Difference between revisions of "Alopecia - Hair Loss"

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{{TOCrightEx}}
 
{{TOCrightEx}}
 
== Rationale ==
 
== Rationale ==
−
* "Medication for men plagued by hair loss has become a topic of interest in Japan since a drug company began marketing it at the end of last year." March 5th, 2006 – [http://stophair.setupmyblog.com/?p=55]
+
* "Medication for men plagued by hair loss has become a topic of interest in Japan since a drug company began marketing it at the end of last year." March 5th, 2006 – [http://stophair.setupmyblog.com/?p=55 Source]
−
 
+
* "An increasing number of companies are apparently turning the Chinese fear of a bald spot into big bucks with some doing so well they are branching out into other countries." February 16, 2006 – [http://stophair.setupmyblog.com/ Source]
−
* "An increasing number of companies are apparently turning the Chinese fear of a bald spot into big bucks with some doing so well they are branching out into other countries." February 16, 2006 – [http://stophair.setupmyblog.com/]
+
* "There is something in the air, or should we say in the hair, these days. Scientific research into hair loss remedies has never been more active or more exciting." June 7, 2006 - [http://www.prnewswire.com/cgi-bin/stories.pl?ACCT=109&STORY=/www/story/06-07-2005/0003821470&EDATE= Source]<br><br>
−
 
+
<br>
−
* "There is something in the air, or should we say in the hair, these days. Scientific research into hair loss remedies has never been more active or more exciting." June 7, 2006 - [http://www.prnewswire.com/cgi-bin/stories.pl?ACCT=109&STORY=/www/story/06-07-2005/0003821470&EDATE=]
+
−
 
+
−
== Alopecia IPMap ==
+
−
[http://www.dolcera.com/client/ds94x0s90akq9d7xb402fm/hairloss_map.htm Dolcera IPMap for Alopecia]
+
  
 
== Introduction ==
 
== Introduction ==
  
−
=== Hair Basics ===
+
=== Hair basics ===
 
* Hair is a complex and delicate part of the body.
 
* Hair is a complex and delicate part of the body.
 
* Keeping it healthy and beautiful is a challenge.
 
* Keeping it healthy and beautiful is a challenge.
−
* Hair grows everywhere on the body with the exception of the lips, eyelids, the palms of the hands and soles of the feet.
+
* Hair grows everywhere on the body with the exception of lips, eyelids, palms of the hands and soles of the feet.
 
* Hair is basically a form of skin.  
 
* Hair is basically a form of skin.  
 
* Hair is made up of a protein called keratin.
 
* Hair is made up of a protein called keratin.
 
* Each shaft of hair is made of two or three inter-twined layers of keratin which grow from a follicle beneath the skin.  
 
* Each shaft of hair is made of two or three inter-twined layers of keratin which grow from a follicle beneath the skin.  
−
* Hair Structure - [http://www.pg.com/science/haircare/hair_twh_12.htm]
+
* Hair Structure - [http://www.pg.com/science/haircare/hair_twh_12.htm Source]
−
* Hair Cycle - [http://www.follicle.com/hair-structure-life-cycle.html]
+
* Hair Cycle - [http://www.follicle.com/hair-structure-life-cycle.html Source]
−
[[Image:Hairbasics.jpg|thumb|center|500px|Structure of Hair root and Hair bulb]]
+
  
−
=== What causes Hair loss? ===       
+
[[Image:Hairbasics.jpg|center|400px|Structure of Hair root and Hair bulb]]
−
* Decreased growth of the hair  
+
 
−
* Increased shedding of the hair  
+
=== What causes hair loss? ===       
−
* Breakage of hairs
+
* Decrease in growth of hair  
 +
* Increase in shedding of hair  
 +
* Breakage of hair
 
* Conversion of thick terminal hairs to thin vellus hairs     
 
* Conversion of thick terminal hairs to thin vellus hairs     
−
[[Image:Facts.jpg|thumb|right|400px|Survey results from Japan]]
+
[[Image:Facts.jpg|thumb|right|250px|Survey results from Japan]]
−
Both men and women lose hair for similar reasons. Hair loss in men is often more dramatic, and follows a specific pattern of loss, one of which has been termed '''“Male Pattern Baldness"''' or '''"Androgenetic Alopecia"'''.
+
Both men and women lose hair for similar reasons. Hair loss in men is often more dramatic, and follows a specific pattern of loss, one of which has been termed “Male Pattern Baldness" or "Androgenetic Alopecia".
−
=== Type of Alopecia===
+
  
−
* '''Alopecia Areata (AA):''' Used to describe hair loss occurring in patches anywhere on the body.
 
−
* '''Alopecia Totalis (AT):''' Total loss of the hair on the scalp.
 
−
* '''Alopecia Universalis (AU):''' Total loss of all hair on the body.
 
−
* '''Alopecia Barbae:''' Loss of facial hair (for a man) especially in the beard area.
 
−
* '''Alopecia Mucinosa:''' A type of alopecia which results in scaley patches.
 
−
* '''Androgenetic Alopecia (AGA)''': Also known as male pattern baldness. It is a thinning of the hair to an almost transparent state, in both men or women. It is thought to be a hereditary form of hair loss.
 
−
* '''Traction Alopecia:''' Traction alopecia is usually due to excessive pulling or tension on hair shafts as a result of certain hair styles. It is seen more often in women, particularly those of East Indian and Afro-Caribbean origin. Hair loss depends on the way the hair is being pulled. Prolonged traction alopecia can stop new hair follicles developing and lead to permanent hair loss.
 
−
* '''Anagen Effluvium:''' This hair loss is generally caused by chemicals such as those used to treat cancer. Initially it causes patchy hair loss, which often then becomes total hair loss. The good news is that when you stop using these chemicals the hair normally grows back (usually about 6 months later). Other drugs also can cause hair loss. Many medicines used to treat even common diseases can cause hair loss.
 
−
* '''Scarring Alopecia:''' A form of alopecia which leaves scarring on the area of hair loss.
 
−
* '''Telogen Effluvium:''' A form of hair loss where more than normal amounts of hair fall out. There is a general 'thinning' of the hair. Unlike some other hair and scalp conditions, it is temporary and the hair growth usually recovers. [http://www.alopeciaonline.org.uk/about/types.asp source]
 
  
−
=== Androgenetic Alopecia ===
+
=== Types of alopecia===
−
* Gradual Onset.
+
−
* Transition from large, thick, pigmented terminal hairs to thinner, shorter, indeterminate hairs and finally to short, wispy, nonpigmented vellus hairs in the involved areas.
+
−
* Characterised by a receding hairline and/or hair loss on the top of the head.
+
  
−
'''Main Causes'''
+
* Alopecia Areata (AA): Hair loss occurring in patches anywhere on the body.
 +
* Alopecia Totalis (AT): Total loss of the hair on the scalp.
 +
* Alopecia Universalis (AU): Total loss of all hair on the body.
 +
* Alopecia Barbae: Loss of facial hair (for a man) especially in the beard area.
 +
* Alopecia Mucinosa: A type of alopecia which results in scaley patches.
 +
* Androgenetic Alopecia (AGA): Also known as male pattern baldness. It is a thinning of the hair to an almost transparent state, in both men or women. It is thought to be a hereditary form of hair loss.
 +
* Traction Alopecia: Traction alopecia is usually due to excessive pulling or tension on hair shafts as a result of certain hair styles. It is seen more often in women, particularly those of East Indian and Afro-Caribbean origin. Hair loss depends on the way the hair is being pulled. Prolonged traction alopecia can stop new hair follicles from developing and leads to permanent hair loss.
 +
* Anagen Effluvium: This hair loss is generally caused by chemicals such as those used to treat cancer. Initially it causes patchy hair loss, which often then leads to total hair loss. The good news is that when you stop using these chemicals the hair normally grows back (usually about 6 months later). Other drugs also can cause hair loss. Many medicines used to treat even common diseases can cause hair loss.
 +
* Scarring Alopecia: A form of alopecia which leaves scarring on the area of hair loss.
 +
* Telogen Effluvium: A form of hair loss where more than normal numbers of hair fall out. There is a general 'thinning' of the hair. Unlike some other hair and scalp conditions, it is temporary and the hair growth usually recovers. ([http://www.alopeciaonline.org.uk/about/types.asp Source])
 +
 
 +
=== Androgenetic alopecia ===
 +
* Gradual onset
 +
* Transition from large, thick, pigmented terminal hairs to thinner, shorter, indeterminate hairs and finally to short, wispy, non-pigmented vellus hairs in the involved areas
 +
* Characterized by a receding hairline and/or hair loss on the top of the head
 +
 
 +
'''Main causes'''
 
* Genetic predisposition
 
* Genetic predisposition
 
* Hormonal effect of androgen  
 
* Hormonal effect of androgen  
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(JICST-EPlus - Japanese Science & Technology)
 
(JICST-EPlus - Japanese Science & Technology)
  
−
== Goals ==
+
== IP activity over the years ==
−
 
+
−
The goal of this report is to:
+
−
* Summarize IP activity over the years
+
−
* Identify major players
+
−
* Conduct patent analysis
+
−
a) Composition
+
−
b) Nature
+
−
c) Action
+
−
 
+
−
'''And then'''
+
−
 
+
−
* Analyze patents pertaining to high sebum activity
+
−
 
+
−
== Approach ==
+
−
 
+
−
* A broad search was conducted on hair loss patents.
+
−
* Patent information was sourced through SIP.
+
−
* A set of patents was selected for analysis.
+
−
 
+
−
Composition of treatment for causes are identified and categorized as follows:
+
−
 
+
−
* Anti-androgen
+
−
* Minoxidil
+
−
* Double action (Anti-androgen + Mindoxidil)
+
−
* Hair matrix cells activator
+
−
* Sebum production inhibitor
+
−
 
+
−
== IP activity over years ==
+
 
The graph indicates:
 
The graph indicates:
 
* Number of patents filed every 5 years (except for first 7 years).
 
* Number of patents filed every 5 years (except for first 7 years).
Line 96: Line 67:
 
[[Image:Year1.jpg|thumb|center|400px|IP Activity over years]]
 
[[Image:Year1.jpg|thumb|center|400px|IP Activity over years]]
  
−
== Major Players ==
+
== Major players ==
−
[[Image:players.jpg|thumb|left|400px|Assignees with more than 20 patents ]]
+
[[Image:players.jpg|thumb|left|500px|Assignees with more than 20 patents ]]
−
[[Image:players1.jpg|thumb|center|400px|Assignees with fewer than 20 patents ]]<br>
+
[[Image:players1.jpg|thumb|center|500px|Assignees with fewer than 20 patents ]]<br>
  
−
* '''Active Assignees'''
+
* '''Active assignees'''
 
Assignees currently active with more than 5 patents to their credit during 2000-2005.  
 
Assignees currently active with more than 5 patents to their credit during 2000-2005.  
 
* Warner with 9 patents,
 
* Warner with 9 patents,
Line 108: Line 79:
 
[[Image:Active.jpg|thumb|center|500px|Active Assignees]]
 
[[Image:Active.jpg|thumb|center|500px|Active Assignees]]
  
−
== Anti-androgens ==  
+
== Taxonomy ==
 +
 
 +
[[Image:Alopecia toxonomy.jpg|thumb|center|800px]]
 +
 
 +
== Interactive Taxonomy ==
 +
''Use the mouse(click and drag/scroll up or down/click on nodes) to explore nodes in the detailed taxonomy'' <br>
 +
''Click on the red arrow on the side of a node name to view the content for that particular node in the dashboard''
 +
 
 +
<mm>[[Map12.mm]]</mm>
 +
 
 +
== Treatment Approaches==
 +
Composition of treatment for causes are identified and categorized as follows:
 +
 
 +
* Anti-androgens (Finasteride) [http://www.emedicine.com/DERM/topic21.htm source]
 +
* Vasodilators (Minoxidil) [http://www.emedicine.com/DERM/topic21.htm source]
 +
* Double action (Anti-androgen + Vasodilator)
 +
* Hair matrix cells activator
 +
 
 +
{|border="1" cellpadding="2", style="#008080" align="center"
 +
|- style="font-weight:bold"  valign="top"
 +
! Cause !! Treatment approach !! Pathways affected
 +
 
 +
|-  valign="top"
 +
| Hormonal effect of androgen || Anti-androgens || Testosterone pathway
 +
 
 +
|-  valign="top"
 +
| Reduction of blood circulation around hair follicle || Vasodilators (eg. Minoxidil) || NO/cGMP Pathway
 +
 
 +
|-  valign="top"
 +
| Deactivation of hair matrix cells || Hair matrix cells activator
 +
|
 +
* Wnt pathway
 +
* STAT pathway
 +
* TGF beta/BMP Pathway
 +
* FGF Pathway
 +
* MAPK Pathway
 +
* NOTCH Pathway
 +
* Hedgehog Pathway
 +
|}
 +
 
 +
=== Anti-androgens ===
 
* Anti-androgens are used in hormone therapy.
 
* Anti-androgens are used in hormone therapy.
 
* Anti-androgens are designed to affect the hormones made in the adrenal glands. They don't stop the hormones from being made, but they stop them from having an effect leading to hair loss.
 
* Anti-androgens are designed to affect the hormones made in the adrenal glands. They don't stop the hormones from being made, but they stop them from having an effect leading to hair loss.
−
 
  
 
'''What causes hair loss?'''
 
'''What causes hair loss?'''
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* Upon binding of anti-androgen in place of DHT, follicle miniaturization is lowered and hair loss prevented.
 
* Upon binding of anti-androgen in place of DHT, follicle miniaturization is lowered and hair loss prevented.
  
−
=== Functions of Anti-androgen ===  
+
==== Functions of Anti-androgen ====  
 
[http://www.revivogen.com/revivogen/work.html Anti-androgen]
 
[http://www.revivogen.com/revivogen/work.html Anti-androgen]
  
 
[[Image:Andogen1.jpg|thumb|center|500px|Functions of Anti-androgen]]
 
[[Image:Andogen1.jpg|thumb|center|500px|Functions of Anti-androgen]]
  
−
=== IP Map for Anti-androgen ===
+
==== IP Map for anti-androgen ====
  
−
{| border="1" cellpadding="8", style="#008080"
+
{| border="1" cellpadding="0", style="#008080"
−
!width="30" bgcolor=DodgerBlue|'''Pat/Pub#'''
+
!width="120" bgcolor=DodgerBlue|'''Pat/Pub#'''
−
!width="30" bgcolor=DodgerBlue|'''Nature'''
+
!width="100" bgcolor=DodgerBlue|'''Nature'''
−
!width="300" bgcolor=DodgerBlue|'''Composition'''  
+
!width="450" bgcolor=DodgerBlue|'''Composition'''  
−
!width="200" bgcolor=DodgerBlue|'''Composition action'''
+
!width="400" bgcolor=DodgerBlue|'''Composition action'''
 
|- style="height:20px"  
 
|- style="height:20px"  
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220060009430%22.PGNR.&OS=DN/20060009430&RS=DN/20060009430 US20060009430]  
+
|bgcolor=LightCyan|[[US20060009430]]  
 
BLOTECH (2004)
 
BLOTECH (2004)
 
|bgcolor=LightCyan|Natural extracts
 
|bgcolor=LightCyan|Natural extracts
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|bgcolor=LightCyan|Organic compound
 
|bgcolor=LightCyan|Organic compound
 
|bgcolor=LightCyan|New class of 4-cycloalkoxy benzonitrile derivatives and salts
 
|bgcolor=LightCyan|New class of 4-cycloalkoxy benzonitrile derivatives and salts
−
|bgcolor=LightCyan|Acts as androgen receptor modulators and blocks formation of DHT.
+
|bgcolor=LightCyan|Acts as androgen receptor modulator and blocks formation of DHT.
 
|- style="height:20px"  
 
|- style="height:20px"  
 
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220050085467%22.PGNR.&OS=DN/20050085467&RS=DN/20050085467 US20050085467]
 
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220050085467%22.PGNR.&OS=DN/20050085467&RS=DN/20050085467 US20050085467]
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|bgcolor=LightCyan|Peptides/nucleic acid
 
|bgcolor=LightCyan|Peptides/nucleic acid
 
|bgcolor=LightCyan|Bradykinin antagonist (peptide of plasma origin from kininogen precursor-kallikrein)
 
|bgcolor=LightCyan|Bradykinin antagonist (peptide of plasma origin from kininogen precursor-kallikrein)
−
|bgcolor=LightCyan|Inhibit synthesis of bradykinin receptors or compounds by binding to B2 receptor
+
|bgcolor=LightCyan|Inhibits synthesis of bradykinin receptors or compounds by binding to B2 receptor
 
|- style="height:20px"  
 
|- style="height:20px"  
 
|bgcolor=LightCyan|[http://v3.espacenet.com/textdoc?DB=EPODOC&IDX=EP0279010&F=0 EP0279010]
 
|bgcolor=LightCyan|[http://v3.espacenet.com/textdoc?DB=EPODOC&IDX=EP0279010&F=0 EP0279010]
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|}
 
|}
  
−
== Minoxidil ==
+
=== Minoxidil (Vasodilators) ===
 
* Minoxidil is a "potassium channel opener" that leads to vasodilation.
 
* Minoxidil is a "potassium channel opener" that leads to vasodilation.
 
* The drug is available in two forms. Oral minoxidil is used to treat high blood pressure and the topical solution form is used to treat hair loss and baldness.
 
* The drug is available in two forms. Oral minoxidil is used to treat high blood pressure and the topical solution form is used to treat hair loss and baldness.
−
 
  
 
'''What causes hair loss?'''
 
'''What causes hair loss?'''
−
* A thick network of tiny veins and arteries lines the outer wall of the follicle. Blood pumps through the bulb and hair via this network.
+
* A thick network of tiny veins and arteries line the outer wall of the follicle. Blood pumps through the bulb and hair via this network.
 
* DHT accumulates in the hair follicles and roots, constricting the blood supply of oxygen and nutrients to the hair roots; which is also seen to possibly contribute towards hair loss.
 
* DHT accumulates in the hair follicles and roots, constricting the blood supply of oxygen and nutrients to the hair roots; which is also seen to possibly contribute towards hair loss.
  
−
'''How does Minoxidal treat hair loss?'''
+
'''How does Minoxidil treat hair loss?'''
−
* Minoxidal is applied to the scalp topically, where it dilates blood vessels in the scalp and sustains the hair follicles for longer period of time.
+
* Minoxidil is applied to the scalp topically, where it dilates blood vessels in the scalp and sustains the hair follicles for longer period of time.
−
* Minoxidil is thought to have a direct mitogenic effect on epidermal cells, as has been observed both in vitro in vivo. Though the mechanism of its action for causing cell proliferation is not very clear, minoxidil is thought to prevent intracellular calcium entry. Calcium normally enhances epidermal growth factors to inhibit hair growth, and Minoxidil by getting converted to minoxidil sulfate acts as a potassium channel agonist and enhances potassium ion permeability to prevent calcium ions from entering into cells.[http://www.hairtransplantadvice.com/medical-hair-restoration.php source]
+
* Minoxidil is thought to have a direct mitogenic effect on epidermal cells, as has been observed both in vitro and in vivo. Though the mechanism of its action for causing cell proliferation is not very clear, minoxidil is thought to prevent intracellular calcium entry. Calcium normally enhances epidermal growth factors to inhibit hair growth, and Minoxidil by getting converted to minoxidil sulfate acts as a potassium channel agonist and enhances potassium ion permeability to prevent calcium ions from entering into cells. ([http://www.hairtransplantadvice.com/medical-hair-restoration.php Source])
 
* Minoxidil sulfate (MS) appears to be the active metabolite responsible for hair growth stimulation.
 
* Minoxidil sulfate (MS) appears to be the active metabolite responsible for hair growth stimulation.
  
−
=== Functions of Monoxidil ===  
+
==== Functions of Vasodilators ====  
  
 
[[Image:minoxidil1.jpg|thumb|center|500px|Functions of Monoxidil [http://www.nurseminerva.co.uk/diagrams.htm#Diagram%201 source]]]
 
[[Image:minoxidil1.jpg|thumb|center|500px|Functions of Monoxidil [http://www.nurseminerva.co.uk/diagrams.htm#Diagram%201 source]]]
  
−
=== IP Map for Minoxidil ===
+
==== IP Map for Vasodilators ====
  
 
{| border="1" cellpadding="2"
 
{| border="1" cellpadding="2"
−
!width="100" bgcolor=DodgerBlue|'''Pat/Pub#'''
+
!width="120" bgcolor=DodgerBlue|'''Pat/Pub#'''
 
!width="75" bgcolor=DodgerBlue|'''Nature'''
 
!width="75" bgcolor=DodgerBlue|'''Nature'''
−
!width="300" bgcolor=DodgerBlue|'''Composition'''
+
!width="600" bgcolor=DodgerBlue|'''Composition'''
 
!width="300" bgcolor=DodgerBlue|'''Composition action'''
 
!width="300" bgcolor=DodgerBlue|'''Composition action'''
 
|- style="height:100px"  
 
|- style="height:100px"  
Line 228: Line 237:
 
|}
 
|}
  
−
== Double action (Anti-androgen + Minoxidil) ==
+
=== Double action (Anti-androgen + Vasodilator) ===
−
* Combination of Minoxidil + Anti-androgen (double action) composition for effective treatment of Male-Pattern Baldness.
+
* Combination of Vasodilator + Anti-androgen (double action) composition for effective treatment of Male-Pattern Baldness.
−
 
+
  
 
'''What is the problem with using only Anti-androgen therapy?'''
 
'''What is the problem with using only Anti-androgen therapy?'''
 
* Anti-androgen is not effective in addressing the issue of vasocontriction around hair follicles due to sebum oil build up.
 
* Anti-androgen is not effective in addressing the issue of vasocontriction around hair follicles due to sebum oil build up.
−
* Anti-androgen only prevent binding of DHT to androgen receptors. However, the effects of improper oxygen and nutrient supply to the brain due to vasocontriction still remains and gradually causes hair loss.
+
* Anti-androgen only prevents binding of DHT to androgen receptors. However, the effects of improper oxygen and nutrient supply to the brain due to vasocontriction still remains and gradually causes hair loss.
  
−
'''What is the problem with using only Minoxidal therapy?'''
+
'''What is the problem with using only Vasodilator (or Minoxidil only) therapy?'''
−
* Minoxidil-based products are generally not effective in stopping hair loss as minoxidil does not block the harmful effects of DHT in the scalp and hair follicles.  
+
* Vasodilator or Minoxidil-based products are generally not effective in stopping hair loss as vasodilators (or Minoxidil) do not block the harmful effects of DHT in the scalp and hair follicles.  
−
* Minoxidil simply dilates blood vessels in the scalp. However, the harmful DHT is still being produced in the body and still getting into the scalp and hair follicles and causing eventual hair loss.
+
* Vasodilators or Minoxidil simply dilate blood vessels in the scalp. However, the harmful DHT still gets produced in the body, enters the scalp and hair follicles causing hair loss.
  
−
'''How is the combination of Anti-androgens and Minoxidil effective?'''
+
'''How is the combination of Anti-androgens and Vasodilator (or Minoxidil) effective?'''
 
* Anti-androgens target the problem of DHT binding to androgen receptors and prevents follicle miniaturization.
 
* Anti-androgens target the problem of DHT binding to androgen receptors and prevents follicle miniaturization.
−
* Minoxidil causes vasodilation and therefore improves supply of oxygen and nutrients to the hair follicle and roots.
+
* Vasodilators like Minoxidil cause vasodilation and therefore improve supply of oxygen and nutrients to the hair follicle and roots.
 
* Combination therapy therefore proves to be much more effective than individual therapy.
 
* Combination therapy therefore proves to be much more effective than individual therapy.
  
−
=== Functions of (Anti-androgen + Minoxidil) === [http://www.revivogen.com/revivogen/work.html Anti-androgen ]and [http://www.xandrox.net/articles/article01.htm Minoxidil]
+
==== Functions of (Anti-androgen + Vasodilators) ====
−
[[Image:Doubleaction1.jpg|thumb|center|500px|Functions of (Anti-androgen + Minoxidil)]]
+
[http://www.revivogen.com/revivogen/work.html Anti-androgen ]and [http://www.xandrox.net/articles/article01.htm Minoxidil]
 +
[[Image:Doubleaction1.jpg|thumb|center|500px|Functions of (Anti-androgen + Vasodilators)]]
  
−
=== IP Map for (Anti-androgen + Minoxidil) ===
+
==== IP Map for (Anti-androgen + Vasodilators) ====
 
{| border="1" cellpadding="3"
 
{| border="1" cellpadding="3"
−
!width="100" bgcolor=DodgerBlue|'''Pat/Pub#'''
+
!width="120" bgcolor=DodgerBlue|'''Pat/Pub#'''
 
!width="75" bgcolor=DodgerBlue|'''Nature'''
 
!width="75" bgcolor=DodgerBlue|'''Nature'''
−
!width="300" bgcolor=DodgerBlue|'''Composition'''  
+
!width="500" bgcolor=DodgerBlue|'''Composition'''  
−
!width="300" bgcolor=DodgerBlue|'''Composition action'''
+
!width="500" bgcolor=DodgerBlue|'''Composition action'''
 
|- style="height:100px"  
 
|- style="height:100px"  
 
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220060052405%22.PGNR.&OS=DN/20060052405&RS=DN/20060052405 US20060052405]  
 
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220060052405%22.PGNR.&OS=DN/20060052405&RS=DN/20060052405 US20060052405]  
 
N/A(2000)
 
N/A(2000)
 
|bgcolor=LightCyan|Peptides
 
|bgcolor=LightCyan|Peptides
−
|bgcolor=LightCyan|Testosterone blocker or vascular toner (Flutamide, cyproterone acetate, spironolactone, progesterone, or analogs or derivatives) and minoxidil mixed along with non-retinoid penetration enhance and sunscreen
+
|bgcolor=LightCyan|Testosterone blocker or vascular toner (Flutamide, cyproterone acetate, spironolactone, progesterone, or analogs or derivatives) and minoxidil mixed along with non-retinoid penetration enhancer and sunscreen
 
|bgcolor=LightCyan|Inhibits 5.alpha.-reductase activity (block DHT) and increase blood flow on the scalp
 
|bgcolor=LightCyan|Inhibits 5.alpha.-reductase activity (block DHT) and increase blood flow on the scalp
 
|- style="height:100px"  
 
|- style="height:100px"  
Line 274: Line 283:
 
|}
 
|}
  
−
 
+
=== Hair matrix cell activator ===
−
== Hair matrix cell activator ==
+
 
Hair matrix cell activator is a substance that acts at the matrix cells in the hair follicle preventing their degradation.
 
Hair matrix cell activator is a substance that acts at the matrix cells in the hair follicle preventing their degradation.
−
 
  
 
'''What causes hair loss?'''
 
'''What causes hair loss?'''
Line 291: Line 298:
 
* Matrix activator allows activation of hair matrix cells and therefore follicle stimulation leading to hair growth.
 
* Matrix activator allows activation of hair matrix cells and therefore follicle stimulation leading to hair growth.
  
−
=== Functions of Hair matrix cell activator === [http://www.ijdb.ehu.es/fullaccess/fulltext.04023/ft163.pdf Hair matrix cell activator]
+
==== Functions of Hair matrix cell activator ====
 +
[http://www.ijdb.ehu.es/fullaccess/fulltext.04023/ft163.pdf Hair matrix cell activator]
 
[[Image:Hair matrix.jpg|thumb|center|500px|Functions of Hair matrix cell activator ]]
 
[[Image:Hair matrix.jpg|thumb|center|500px|Functions of Hair matrix cell activator ]]
  
−
=== IP Map for Hair matrix cell activator ===
+
==== IP Map for Hair matrix cell activator ====
 
{| border="1" cellpadding="2"
 
{| border="1" cellpadding="2"
−
!width="100" bgcolor=DodgerBlue|'''Pat/Pub#'''
+
!width="120" bgcolor=DodgerBlue|'''Pat/Pub#'''
−
!width="75" bgcolor=DodgerBlue|'''Nature'''
+
!width="100" bgcolor=DodgerBlue|'''Nature'''
−
!width="300" bgcolor=DodgerBlue|'''Composition'''  
+
!width="200" bgcolor=DodgerBlue|'''Composition'''  
−
!width="300" bgcolor=DodgerBlue|'''Composition action'''
+
!width="600" bgcolor=DodgerBlue|'''Composition action'''
−
|- style="height:100px"  
+
|- style="height:50px"  
 
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220020052498%22.PGNR.&OS=DN/20020052498&RS=DN/20020052498 US20020052498]
 
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220020052498%22.PGNR.&OS=DN/20020052498&RS=DN/20020052498 US20020052498]
 
SHISEIDO(1999)  
 
SHISEIDO(1999)  
Line 306: Line 314:
 
|bgcolor=LightCyan|(2-substituted oxyphenyl) alkanamide derivative and its salt
 
|bgcolor=LightCyan|(2-substituted oxyphenyl) alkanamide derivative and its salt
 
|bgcolor=LightCyan|Mechanism of action has not been made clear, having excellent hair follicle activating action and regrowth promoting effect
 
|bgcolor=LightCyan|Mechanism of action has not been made clear, having excellent hair follicle activating action and regrowth promoting effect
−
|- style="height:100px"  
+
|- style="height:50px"  
 
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220040071647%22.PGNR.&OS=DN/20040071647&RS=DN/20040071647 US20040071647]
 
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220040071647%22.PGNR.&OS=DN/20040071647&RS=DN/20040071647 US20040071647]
 
L'OREAL(1998)  
 
L'OREAL(1998)  
 
|bgcolor=LightCyan|Peptides
 
|bgcolor=LightCyan|Peptides
 
|bgcolor=LightCyan|Metalloprotease (MMP-9) inhibitor (thiol or a hydroxamate) other than chelating calcium ions
 
|bgcolor=LightCyan|Metalloprotease (MMP-9) inhibitor (thiol or a hydroxamate) other than chelating calcium ions
−
|bgcolor=LightCyan|Reducing the expression of MMPs (Metalloproteases) in the scalp - slow down or inhibit the degradation of the perifollicular matrix (extracellular matrix surround the hair follicle)  
+
|bgcolor=LightCyan|Reducing the expression of MMPs (Metalloproteases) in the scalp - slows down or inhibits the degradation of the perifollicular matrix (extracellular matrix surrounding the hair follicle)  
−
|}
+
−
 
+
−
== Sebum Production Inhibitor ==
+
−
Sebum Production Inhibitor is a substance that prevents the synthesis of sebum, mixture of lipid substances.
+
−
 
+
−
'''What causes hair loss?'''
+
−
* Sebum is a fatty acid substance secreted from sebaceous glands associated with hair follicles.
+
−
* Hair can get heavy sebum build-up and mixes with cholesterol to form a hardened plug around the bottom part of the hair bulb.
+
−
* Hardened plugs prevent cell respirations and eventually lead to hair loss.
+
−
* Bacteria will also attach to the hardened plug and this can also cause further cause problems with hair growth.
+
−
 
+
−
'''How does Sebum production inhibitor treat hair loss?'''
+
−
* The inhibitor prevents synthesis of sebum and slows down accumulation and mixing of sebum with cholesterol leading to hardened plugs.
+
−
* Reduction of sebum results in unclogged hair follicles/bulbs and allows oxygen and nutrients from reaching the hair follicle.
+
−
* Reduction in sebum also prevents vasoconstriction.
+
−
* Sum result of these effects of Sebum production inhibitor is prevention of hair loss.
+
−
 
+
−
 
+
−
* The inhibitor blocks the excessive sebum production produces greasy effect on hair and scalp and also responsible for thinning and loosing of hair.
+
−
 
+
−
=== Functions of Sebum Production Inhibitor ===
+
−
[[http://en.wikipedia.org/wiki/Image:HairFollicle.jpg Sebum Production Inhibitor]]
+
−
[[Image:Sebum1.jpg|thumb|center|500px|Functions of Sebum Production Inhibitor]]
+
−
 
+
−
=== IPMap for Sebum Production Inhibitor ===
+
−
+
−
{| border="1" cellpadding="3", style="#008080"
+
−
!width="100" bgcolor=DodgerBlue|'''Pat/Pub#'''
+
−
!width="75" bgcolor=DodgerBlue|'''Nature'''
+
−
!width="300" bgcolor=DodgerBlue|'''Composition'''
+
−
!width="300" bgcolor=DodgerBlue|'''Composition action'''
+
−
|- style="height:100px"
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220050277699%22.PGNR.&OS=DN/20050277699&RS=DN/20050277699 US20050277699]
+
−
Unilever(2005)
+
−
|bgcolor=LightCyan|Natural extract and organic compound
+
−
|bgcolor=LightCyan|Polyamine (putrescine, spermine or spermidine) analogs and/or derivatives; DFMO; N-acetyl cysteines; neutralized salts of a non-hydroxy C2-C40 dicarboxylic acids, preferably malonate salts; and mixtures thereof.
+
−
|bgcolor=LightCyan|Decreasing sebum production and/or pore size
+
−
|- style="height:100px"
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220050244362%22.PGNR.&OS=DN/20050244362&RS=DN/20050244362 US20050244362]
+
−
KAO COPR.(2004)
+
−
|bgcolor=LightCyan|Natural extract and organic compound
+
−
|bgcolor=LightCyan|Avocado oil (Butyl esters of fatty acids)
+
−
|bgcolor=LightCyan|Reduce sebum of the hair and scalp
+
−
|- style="height:100px"
+
−
|bgcolor=LightCyan|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=4529587.PN.&OS=PN/4529587&RS=PN/4529587 US4529587]
+
−
Unilever(1982)
+
−
|bgcolor=LightCyan|organic compound
+
−
|bgcolor=LightCyan |Biotin antagonist or a salt thereof 
+
−
|bgcolor=LightCyan|Decrease activity of the enzyme acetyl-SCoA-carboxylase and hence reduce lipid synthesis in sebaceous glands so that less sebum is produced
+
 
|}
 
|}
  
−
== Composition nature matrix ==
+
== Technology mapping based on patents analyzed ==
  
 
=== IPMap: Composition nature matrix ===
 
=== IPMap: Composition nature matrix ===
  
 
{| border="1" cellpadding="11", style="#008080"
 
{| border="1" cellpadding="11", style="#008080"
−
!width="50" bgcolor=DodgerBlue|'''Year'''
+
!width="120" bgcolor=DodgerBlue|'''Year'''
−
!width="75" bgcolor=DodgerBlue|'''Organic Compound'''
+
!width="200" bgcolor=DodgerBlue|'''Organic Compound'''
−
!width="75" bgcolor=DodgerBlue|'''Natural extracts'''  
+
!width="200" bgcolor=DodgerBlue|'''Natural extracts'''  
−
!width="75" bgcolor=DodgerBlue|'''Peptides'''
+
!width="200" bgcolor=DodgerBlue|'''Peptides'''
−
!width="75" bgcolor=DodgerBlue|'''Nucleotides'''
+
!width="200" bgcolor=DodgerBlue|'''Nucleotides'''
−
!width="75" bgcolor=DodgerBlue|'''Natural extract + Organic comp'''
+
!width="200" bgcolor=DodgerBlue|'''Natural extract + Organic comp'''
 
|- style="height:10px"
 
|- style="height:10px"
 
|bgcolor=LightCyan|2005  
 
|bgcolor=LightCyan|2005  
Line 393: Line 352:
 
|bgcolor=LightCyan|APHIOS (1)  
 
|bgcolor=LightCyan|APHIOS (1)  
 
|bgcolor=LightCyan|....
 
|bgcolor=LightCyan|....
−
|bgcolor=LightCyan|FUNDIACION (1)
+
|bgcolor=LightCyan|FUNDACION (1)
 
|bgcolor=LightCyan|....
 
|bgcolor=LightCyan|....
 
|-  
 
|-  
Line 452: Line 411:
 
|bgcolor=LightCyan|....
 
|bgcolor=LightCyan|....
 
|}
 
|}
−
 
+
=== Focus of patents ===
−
== Focus of patents ==
+
  
 
{| border="1" cellpadding="17", style="#008080"
 
{| border="1" cellpadding="17", style="#008080"
−
!width="600" bgcolor=DodgerBlue|'''Focus of patents'''
+
!width="800" bgcolor=DodgerBlue|'''Focus of patents'''
−
!width="20" bgcolor=DodgerBlue|'''Patent no.'''
+
!width="150" bgcolor=DodgerBlue|'''Patent no.'''
−
!width="20" bgcolor=DodgerBlue|'''Rec. no.'''
+
!width="100" bgcolor=DodgerBlue|'''Rec. no.'''
 
|-   
 
|-   
 
|bgcolor=LightCyan|2-substituted oxyphenyl alkanamide derivative having excellent hair growth effect.
 
|bgcolor=LightCyan|2-substituted oxyphenyl alkanamide derivative having excellent hair growth effect.
Line 529: Line 487:
 
|}
 
|}
  
−
=== Focus of patents by technology ===
+
=== Technology focus===
 
[[Image:Technologyfocus2.jpg|thumb|center|700px|Technology focus]]
 
[[Image:Technologyfocus2.jpg|thumb|center|700px|Technology focus]]
−
 
+
=== Distribution of patents ===
−
== Distribution of patents ==
+
 
   
 
   
−
=== By patent types ===
+
==== By patent types ====
 
[[Image:Didtribution.jpg|thumb|center|700px|Distribution based on patent types ]]
 
[[Image:Didtribution.jpg|thumb|center|700px|Distribution based on patent types ]]
  
  
−
=== By key ingredients ===
+
==== By key ingredients ====
 
[[Image:key1.jpg|thumb|center|700px|Distribution of key ingredients]]
 
[[Image:key1.jpg|thumb|center|700px|Distribution of key ingredients]]
  
−
=== By target disease ===
+
==== By target disease ====
 
[[Image:target.jpg|thumb|center|700px|Distribution based on target diseases]]
 
[[Image:target.jpg|thumb|center|700px|Distribution based on target diseases]]
  
  
−
=== Key ingredients vs. Target disease ===
+
==== Key ingredients vs. Target disease ====
 
[[Image:key&target1.jpg|thumb|center|1000px|Key ingredients vs. Target disease]]
 
[[Image:key&target1.jpg|thumb|center|1000px|Key ingredients vs. Target disease]]
  
  
−
=== Target species ===
+
==== Target species ====
 
[[Image:Species.jpg|thumb|center|700px|Target species]]
 
[[Image:Species.jpg|thumb|center|700px|Target species]]
  
  
−
=== Mode of administration ===
+
 
 +
==== Mode of administration ====
 
[[Image:Mode.jpg|thumb|center|700px|Mode of administration]]
 
[[Image:Mode.jpg|thumb|center|700px|Mode of administration]]
  
  
−
=== Product type vs. Product form ===
+
==== Product type vs. Product form ====
 
[[Image:prod.jpg|thumb|center|700px|Product type vs. Product form]]
 
[[Image:prod.jpg|thumb|center|700px|Product type vs. Product form]]
  
−
== Distribution based on different aspects ==
+
==== Patents by target diseases ====
−
 
+
−
=== List of patents ===
+
−
{| border="1" cellpadding="9", style="#008080"
+
−
!width="20" bgcolor=DodgerBlue|'''Rec. no.'''
+
−
!width="70" bgcolor=DodgerBlue|'''Patent no.'''
+
−
!width="20" bgcolor=DodgerBlue|'''Rec. no.'''
+
−
!width="70" bgcolor=DodgerBlue|'''Patent no.'''
+
−
|- style="height:10px"
+
−
|bgcolor=LightCyan|1
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220020052498%22.PGNR.&OS=DN/20020052498&RS=DN/20020052498 US20020052498]
+
−
|bgcolor=LightCyan|10
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220040157856%22.PGNR.&OS=DN/20040157856&RS=DN/20040157856 US20040157856]
+
−
|-
+
−
|bgcolor=LightCyan|2
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220030007941%22.PGNR.&OS=DN/20030007941&RS=DN/20030007941 US20030007941]
+
−
|bgcolor=LightCyan|11
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220050053572%22.PGNR.&OS=DN/20050053572&RS=DN/20050053572 US20050053572]
+
−
|-
+
−
|bgcolor=LightCyan|3
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220060009430%22.PGNR.&OS=DN/20060009430&RS=DN/20060009430 US20060009430]
+
−
|bgcolor=LightCyan|12
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220060052405%22.PGNR.&OS=DN/20060052405&RS=DN/20060052405 US20060052405]
+
−
|-
+
−
|bgcolor=LightCyan|4
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220060009427%22.PGNR.&OS=DN/20060009427&RS=DN/20060009427 US20060009427]
+
−
|bgcolor=LightCyan|13
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220050123577%22.PGNR.&OS=DN/20050123577&RS=DN/20050123577 US20050123577]
+
−
|-
+
−
|bgcolor=LightCyan|5
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220050118282%22.PGNR.&OS=DN/20050118282&RS=DN/20050118282 US20050118282]
+
−
|bgcolor=LightCyan|14
+
−
|bgcolor=LightCyan|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6447762.PN.&OS=PN/6447762&RS=PN/6447762 US6447762]
+
−
|-
+
−
|bgcolor=LightCyan|6
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220050085467%22.PGNR.&OS=DN/20050085467&RS=DN/20050085467 US20050085467]
+
−
|bgcolor=LightCyan|15
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220040071647%22.PGNR.&OS=DN/20040071647&RS=DN/20040071647 US20040071647]
+
−
|-
+
−
|bgcolor=LightCyan|7
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220060009429%22.PGNR.&OS=DN/20060009429&RS=DN/20060009429 US20060009429]
+
−
|bgcolor=LightCyan|16
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220050277699%22.PGNR.&OS=DN/20050277699&RS=DN/20050277699 US20050277699]
+
−
|-
+
−
|bgcolor=LightCyan|8
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220030073616%22.PGNR.&OS=DN/20030073616&RS=DN/20030073616 US20030073616]
+
−
|bgcolor=LightCyan|17
+
−
|bgcolor=LightCyan|[http://appft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220050244362%22.PGNR.&OS=DN/20050244362&RS=DN/20050244362 US20050244362]
+
−
|-
+
−
|bgcolor=LightCyan|9
+
−
|bgcolor=LightCyan|[http://v3.espacenet.com/textdoc?DB=EPODOC&IDX=EP0279010&F=0 EP0279010]
+
−
|bgcolor=LightCyan|18
+
−
|bgcolor=LightCyan|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=4529587.PN.&OS=PN/4529587&RS=PN/4529587 US4529587]
+
−
|}
+
−
 
+
−
=== Patents by target diseases ===
+
 
{| border="1" cellpadding="16", style="#008080"
 
{| border="1" cellpadding="16", style="#008080"
−
!width="600" bgcolor=DodgerBlue|'''Target disease/ disorder'''
+
!width="800" bgcolor=DodgerBlue|'''Target disease/ disorder'''
−
!width="20" bgcolor=DodgerBlue|'''Patent no.'''
+
!width="150" bgcolor=DodgerBlue|'''Patent no.'''
−
!width="20" bgcolor=DodgerBlue|'''Rec. no.'''
+
!width="150" bgcolor=DodgerBlue|'''Rec. no.'''
 
|-   
 
|-   
 
|bgcolor=LightCyan|Alopecia areata, alopecia pityrodes or alopecia seborrheica, or androgenic alopecia (i.e. male pattern baldness)
 
|bgcolor=LightCyan|Alopecia areata, alopecia pityrodes or alopecia seborrheica, or androgenic alopecia (i.e. male pattern baldness)
Line 686: Line 589:
 
|}
 
|}
  
−
=== Patents by application ===
 
−
[[Image:application.jpg|thumb|center|700px|Distribution of patents based on application]]
 
  
−
=== Signaling Pathway and linkages ===
+
 
 +
==== [[List of patents]] ====
 +
== Pathways and linkages ==
 +
 
 +
=== Pathways associated with hair matrix cell activation===
 +
 
 
'''Molecular mediators of hair follicle embryogenesis:''' Identification of the molecular pathways controlling differentiation and proliferation in mammalian hair follicles provides the crucial link to understanding the regulation of normal hair growth, the basis of hereditary hair loss diseases, and the origin of follicle-based tumors. Homeobox (hox), hedgehog (hh), patched (ptc), wingless (wg}/wnt, disheveled (dsh), engrailed (en), Notch 1 and armadillo/B-catenin genes are all critical for hair follicle.
 
'''Molecular mediators of hair follicle embryogenesis:''' Identification of the molecular pathways controlling differentiation and proliferation in mammalian hair follicles provides the crucial link to understanding the regulation of normal hair growth, the basis of hereditary hair loss diseases, and the origin of follicle-based tumors. Homeobox (hox), hedgehog (hh), patched (ptc), wingless (wg}/wnt, disheveled (dsh), engrailed (en), Notch 1 and armadillo/B-catenin genes are all critical for hair follicle.
  
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* '''FGF Pathway:''' Fibroblast growth factor (bFGF) and platelet-derived growth factor (PDGF) potentiate the growth of dermal papilla cells. It is proposed that these proteins increase the synthesis of stromelysin (an enzyme, matrix metalloproteinase) which acts on the papilla cells and accelerates their growth.
 
* '''FGF Pathway:''' Fibroblast growth factor (bFGF) and platelet-derived growth factor (PDGF) potentiate the growth of dermal papilla cells. It is proposed that these proteins increase the synthesis of stromelysin (an enzyme, matrix metalloproteinase) which acts on the papilla cells and accelerates their growth.
 
* '''MAPK Pathway:''' Mitogen-activated protein kinase (MAPK) activation, increases keratinocyte turnover.
 
* '''MAPK Pathway:''' Mitogen-activated protein kinase (MAPK) activation, increases keratinocyte turnover.
−
* '''Testosterone Pathway'''
 
 
* '''NOTCH Pathway''':  Notch-1 is expressed in ectodermal-derived cells of the follicle, in the inner cells of the embryonic placode and the follicle bulb, and in the suprabasal cells of the mature outer root sheath. Delta-1, one of the three ligands is only expressed during embryonic follicle development and is exclusive to the mesenchymal cells of the pre-papilla located beneath the follicle placode, and appears to promote and accelerate placode formation, while suppressing placode formation in surrounding cells. Other ligands, Serrate 1 and Serrate 2, are expressed in matrix cells destined to form the inner root sheath and hair shaft.
 
* '''NOTCH Pathway''':  Notch-1 is expressed in ectodermal-derived cells of the follicle, in the inner cells of the embryonic placode and the follicle bulb, and in the suprabasal cells of the mature outer root sheath. Delta-1, one of the three ligands is only expressed during embryonic follicle development and is exclusive to the mesenchymal cells of the pre-papilla located beneath the follicle placode, and appears to promote and accelerate placode formation, while suppressing placode formation in surrounding cells. Other ligands, Serrate 1 and Serrate 2, are expressed in matrix cells destined to form the inner root sheath and hair shaft.
  
 +
=== Pathways associated with Anti Androgen===
 +
[[Image:Slide3.gif|center|720 px|Alopecia pathways]]
  
−
 
+
==== Players of WNT inhibition Pathway ====
−
[[Image:Slide1.GIF|thumb|center|700px|Alopecia pathways]]
+
[[Image:wnt.jpg|thumb|right|200 px|Wnt inhibition]]
−
 
+
−
== Players of Wnt inhibition Pathway == [[Image:wnt.jpg|thumb|right|600px|Wnt inhibition]]
+
 
{| border="1" cellpadding="15", style="#008080"
 
{| border="1" cellpadding="15", style="#008080"
−
!width="70" bgcolor=DodgerBlue|'''Patent no.'''
+
!width="150" bgcolor=DodgerBlue|'''Patent no.'''
−
!width="20" bgcolor=DodgerBlue|'''Key compound'''
+
!width="200" bgcolor=DodgerBlue|'''Key compound'''
−
!width="70" bgcolor=DodgerBlue|'''Players of inhibition'''
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!width="200" bgcolor=DodgerBlue|'''Players of inhibition'''
 
|- style="height:10px"
 
|- style="height:10px"
 
|bgcolor=lightyellow|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6664247.PN.&OS=PN/6664247&RS=PN/6664247 US6664247]
 
|bgcolor=lightyellow|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6664247.PN.&OS=PN/6664247&RS=PN/6664247 US6664247]
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|bgcolor=LightCyan|[http://v3.espacenet.com/textdoc?DB=EPODOC&IDX=WO03011287&F=0 WO2003011287]
 
|bgcolor=LightCyan|[http://v3.espacenet.com/textdoc?DB=EPODOC&IDX=WO03011287&F=0 WO2003011287]
 
|bgcolor=LightCyan|Pyrazolon derivatives  
 
|bgcolor=LightCyan|Pyrazolon derivatives  
−
|bgcolor=LightCyan|GSK3, β-catenin
+
|bgcolor=LightCyan|GSK3, ß-catenin
 
|-
 
|-
 
|bgcolor=LightCyan|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6924141.PN.&OS=PN/6924141&RS=PN/6924141 US6924141]
 
|bgcolor=LightCyan|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6924141.PN.&OS=PN/6924141&RS=PN/6924141 US6924141]
 
|bgcolor=LightCyan|Lithium chloride, Wnt3/4/ 7  
 
|bgcolor=LightCyan|Lithium chloride, Wnt3/4/ 7  
−
|bgcolor=LightCyan|β-catenin, GSK3, Wnt
+
|bgcolor=LightCyan|ß-catenin, GSK3, Wnt
 
|-
 
|-
 
|bgcolor=LightCyan|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6706685.PN.&OS=PN/6706685&RS=PN/6706685 US6706685]
 
|bgcolor=LightCyan|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6706685.PN.&OS=PN/6706685&RS=PN/6706685 US6706685]
 
|bgcolor=LightCyan|Peptide sequence  
 
|bgcolor=LightCyan|Peptide sequence  
−
|bgcolor=LightCyan|β-catenin
+
|bgcolor=LightCyan|ß-catenin
 
|-
 
|-
 
|bgcolor=LightCyan|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6683048.PN.&OS=PN/6683048&RS=PN/6683048 US6683048]
 
|bgcolor=LightCyan|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6683048.PN.&OS=PN/6683048&RS=PN/6683048 US6683048]
 
|bgcolor=LightCyan|Peptide sequence  
 
|bgcolor=LightCyan|Peptide sequence  
−
|bgcolor=LightCyan|α-catenin, β-catenin
+
|bgcolor=LightCyan|a-catenin, ß-catenin
 
|-
 
|-
 
|bgcolor=LightCyan|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6677116.PN.&OS=PN/6677116&RS=PN/6677116 US6677116]
 
|bgcolor=LightCyan|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6677116.PN.&OS=PN/6677116&RS=PN/6677116 US6677116]
 
|bgcolor=LightCyan|Peptide sequence  LXXLL
 
|bgcolor=LightCyan|Peptide sequence  LXXLL
−
|bgcolor=LightCyan|β-catenin
+
|bgcolor=LightCyan|ß-catenin
 
|-
 
|-
 
|bgcolor=LightCyan|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6303576.PN.&OS=PN/6303576&RS=PN/6303576 US6303576]
 
|bgcolor=LightCyan|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6303576.PN.&OS=PN/6303576&RS=PN/6303576 US6303576]
 
|bgcolor=LightCyan|Peptide sequence  LXXLL
 
|bgcolor=LightCyan|Peptide sequence  LXXLL
−
|bgcolor=LightCyan|β-catenin
+
|bgcolor=LightCyan|ß-catenin
 
|}
 
|}
−
[[Image:coloury.jpg]]- '''Target sites and Details'''
 
−
 
−
== Pyrazole compounds ==
 
  
 +
==== Role of Pyrazole compounds in Wnt Pathway====
 +
'''Pyrazole'''
 
* '''Pyrazole''' (C3H4N2) refers both to the class of simple aromatic ring organic compounds of the heterocyclic series characterized by a 5-membered ring structure composed of three carbon atoms and two nitrogen atoms in adjacent positions and to the unsubstituted parent compound. Being so composed and having pharmacological effects on humans, they are classified as alkaloids although they are not known to occur in nature.
 
* '''Pyrazole''' (C3H4N2) refers both to the class of simple aromatic ring organic compounds of the heterocyclic series characterized by a 5-membered ring structure composed of three carbon atoms and two nitrogen atoms in adjacent positions and to the unsubstituted parent compound. Being so composed and having pharmacological effects on humans, they are classified as alkaloids although they are not known to occur in nature.
−
* Pyrazoles are produced synthetically through the reaction of α,β-unsaturated aldehydes with hydrazine and subsequent dehydrogenation  
+
* Pyrazoles are produced synthetically through the reaction of a,ß-unsaturated aldehydes with hydrazine and subsequent dehydrogenation  
 
[[Image:pyrazole1.jpg|thumb|center|500px|Pyrazole (C3H4N2)]]
 
[[Image:pyrazole1.jpg|thumb|center|500px|Pyrazole (C3H4N2)]]
 
* Pyrazoles are used for their analgesic, anti-inflammatory, antipyretic, antiarrhythmic, tranquilizing, muscle relaxing, psychoanaleptic, anticonvulsant, monoamineoxidase inhibiting, antidiabetic and antibacterial activities.
 
* Pyrazoles are used for their analgesic, anti-inflammatory, antipyretic, antiarrhythmic, tranquilizing, muscle relaxing, psychoanaleptic, anticonvulsant, monoamineoxidase inhibiting, antidiabetic and antibacterial activities.
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[[Image:pyrazole2.jpg|thumb|center|500px|Structurally related compounds]]
 
[[Image:pyrazole2.jpg|thumb|center|500px|Structurally related compounds]]
  
−
=== GSK3 inhibition by pyrazole compounds ===
+
==== GSK3 inhibition by pyrazole compounds ====
 
[[Image:bold3.jpg]]
 
[[Image:bold3.jpg]]
 
{| border="1" cellpadding="2", style="#008080"
 
{| border="1" cellpadding="2", style="#008080"
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!width="100"|[http://patft1.uspto.gov/netacgi/nph-Parser?TERM1=6989385+&Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=0&f=S&l=50 US6989385]
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!width="350"|[http://patft1.uspto.gov/netacgi/nph-Parser?TERM1=6989385+&Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=0&f=S&l=50 US6989385]
 
[[Image:US6989385.jpg]]
 
[[Image:US6989385.jpg]]
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!width="100"|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6664247.PN.&OS=PN/6664247&RS=PN/6664247 US6664247]  
+
!width="350"|[http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6664247.PN.&OS=PN/6664247&RS=PN/6664247 US6664247]  
 
[[Image:US6664247.jpg]]
 
[[Image:US6664247.jpg]]
−
!width="100"|[http://v3.espacenet.com/textdoc?DB=EPODOC&IDX=WO2005012256&F=0 WO2005012256]  
+
!width="350"|[http://v3.espacenet.com/textdoc?DB=EPODOC&IDX=WO2005012256&F=0 WO2005012256]  
 
[[Image:WO2005012256.jpg]]
 
[[Image:WO2005012256.jpg]]
 
|-  
 
|-  
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|}
 
|}
  
−
=== Inhibition by amine derivatives ===
+
==== Inhibition by amine derivatives ====
  
 
'''Patent Number''': US6989385
 
'''Patent Number''': US6989385
 
'''Applicant''': ''Vertex Pharmaceuticals Incorporated''
 
'''Applicant''': ''Vertex Pharmaceuticals Incorporated''
 
'''Title''': Pyrazole compounds useful as protein kinase inhibitors
 
'''Title''': Pyrazole compounds useful as protein kinase inhibitors
 +
 
'''Basic Structure''':
 
'''Basic Structure''':
  
 
[[Image:pyrazol1.jpeg]]
 
[[Image:pyrazol1.jpeg]]
  
−
'''Derivatives of pyrimidine-pyrazole amine disclosed in the patent:'''
+
[[Derivatives of pyrimidine-pyrazole amine disclosed in US6989385 patent]]
  
−
* [6-(2,6-Dimethylphenyl)-2-(naphthalen-2-ylsulfanyl)-pyrimidin-4-yl]-(5-met- hyl-2H-pyrazol-3-yl)-amine
 
−
* [6-(2-Methylphenyl)-2-(naphthalen-2-ylsulfanyl)-pyrimidin-4-yl]-(5-methyl-- 2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Acetamido-phenylsulfanyl)-6-phenyl-pyrimidin-4-yl]-(5-methyl-2H-pyra- zol-3-yl)-amine
 
−
* [2-(4-Isobutyrylylamino-phenylsulfanyl)-6-phenylpyrimidin-4-yl]-(5-methyl-- 2H-pyrazol-3-yl)-
 
−
* [6-(4-Methylpiperazin-1-yl)-2-methylsulfanyl-pyrimidin-4-yl]-(5-methyl-2H-- pyrazol-3-yl)-amine
 
−
* (5-Methyl-2H-pyrazol-3-yl)-[6-phenyl-2-(4-propionylamino-phenylsulfanyl)-p- yrimidin-4-yl]-amine
 
−
* [2-(4-Cyclopropanecarbonylamino-phenylsulfanyl)-6-phenylpyrimidin-4-yl]-(5- -methyl-2H-pyrazol-3-yl)-amine
 
−
* (5-Methyl-2H-pyrazol-3-yl)-{6-phenyl-2-[4-(propane-1-sulfonylamino)-phenyl- sulfanyl]-pyrimidin-4-yl}-amine
 
−
* [2-(4-Ethanesulfonylamino-phenylsulfanyl)-6-phenyl-pyrimidin-4-yl]-(5-meth- yl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Acetamidophenyl-sulfanyl)-6-(2-methylphenyl)-pyrimidin-4-yl]-(5-meth- yl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Isobutanecarbonylamino-phenyl-sulfanyl)-6-phenyl-pyrimidin-4-yl]-(5-- methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Acetamido-phenyl-sulfanyl)-5-methyl-6-phenyl-pyrimidin-4-yl]-(5-meth- yl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Acetamido-phenyl-sulfanyl)-6-(4-methoxyphenyl)-pyrimidin-4-yl]-(5-me- thyl-2H-pyrazol-3-yl)-amine
 
−
* [6-(3-Acetamidophenyl)-2-(4-acetamido-phenyl-sulfanyl)-pyrimidin-4-yl]-(5-- methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Isopropanesulfonylamino-phenyl-sulfanyl)-6-phenyl-pyrimidin-4-yl]-(5- -methyl-2H-pyrazol-3-yl)-amine
 
−
* {2-[4-(2-Dimethylamino-acetylamino)-phenylsulfanyl]-6-phenyl-pyrimidin-4-y- l}-(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(3-Chloro-benzylsulfanyl)-6-morpholin-4-yl-pyrimidin-4-yl]-(5-methyl-2H- -pyrazol-3-yl)-amine
 
−
* [2-(3-Chloro-benzylsulfanyl)-6-(2-methoxy-ethylamino)-pyrimidin-4-yl]-(5-m- ethyl-2H-pyrazol-3-yl)-amine
 
−
* [2-Benzylsulfanyl-6-(4-methylpiperazin-1-yl)-pyrimidin-4-yl]-(5-methyl-2H-- pyrazol-3-yl)-amine
 
−
* [2-Benzylsulfanyl-6-morpholin-4-yl-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-- yl)-amine
 
−
* [2-(3-Chloro-benzylsulfanyl)-6-(4-methylpiperazin-1-yl)-pyrimidin-4-yl]-(5- -methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-methoxy-benzylsulfanyl)-6-(4-methylpiperazin-1-yl)-pyrimidin-4-yl]-(- 5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Acetamido-phenyl-sulfanyl)-6-tert-butyl-pyrimidin-4-yl]-(5-methyl-2H- -pyrazol-3-yl)-amine
 
−
* (5-Cyclopropyl-2H-pyrazol-3-yl)-[6-phenyl-2-(4-propionylamino-phenyl-sulfa- nyl)-pyrimidin-4-yl]-amine
 
−
* [2-(3-Chloro-benzylsulfanyl)-6-(piperidin-1-yl)-pyrimidin-4-yl]-(5-methyl-- 2H-pyrazol-3-yl)-amine
 
−
* (5-Methyl-2H-pyrazol-3-yl)-{2-[4-(morpholinesulfonyl)-benzylsulfanyl]-6-mo- rpholin-4-yl-pyrimidin-4-yl}-amine
 
−
* {6-(2-Methoxy-ethylamino)-2-[4-(morpholinesulfonyl)-benzylsulfanyl]-pyrimi- din-4-yl}-(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* {6-(4-methylpiperazin-1-yl)-2-[4-(morpholinesulfonyl)-benzylsulfanyl]-pyri- midin-4-yl}-(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [6-Methoxymethyl-2-(4-propionylamino-phenyl-sulfanyl)-pyrimidin-4-yl]-(5-m- ethyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Methoxycarbonyl-phenyl-sulfanyl)-6-methoxymethyl-pyrimidin-4-yl]-(5-- methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(3,5-Dimethoxy-benzylsulfanyl)-6-morpholin-4-yl-pyrimidin-4-yl]-(5-meth- yl-2H-pyrazol-3-yl)-amine
 
−
* [2-(3,5-Dimethoxy-benzylsulfanyl)-6-pyrrolidin-4-yl-pyrimidin-4-yl]-(5-met- hyl-2H-pyrazol-3-yl)-amine
 
−
* 5-Methyl-2H-pyrazol-3-yl)-[6-morpholin-4-yl-2-(naphthalene-2-ylmethylsulf- anyl)-pyrimidin-4-yl]-amine
 
−
* {2-(4-Acetamido-phenyl-sulfanyl)-6-[4-(3-dimethylamino-propoxy)-phenyl]-py- rimidin-4-yl}-(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Acetamidophenylsulfanyl)-6-(morpholin-4-yl)-pyrimidin-4-yl]-(5-methy- l-2H-pyrazol-3-yl)-amine
 
−
* [6-Hydroxymethyl-2-(4-propionylamino-phenyl-sulfanyl)-pyrimidin-4-yl]-(5-m- ethyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Acetamido-phenyl-sulfanyl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl- )-amine
 
−
* [6-(1-Butoxycarbonyl)-2-(4-propionylamino-phenyl-sulfanyl)-pyrimidin-4-yl]- -(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [6-Methoxycarbonyl-2-(4-propionylamino-phenyl-sulfanyl)-pyrimidin-4-yl]-(5- -methyl-2H-pyrazol-3-yl)-amine
 
−
* (5-Methyl-2H-pyrazol-3-yl)-(6-phenyl-2-phenylamino-pyrimidin-4-yl)-amine
 
−
* (5-Cyclopropyl-2H-pyrazol-3-yl)-(6-phenyl-2-phenylamino-pyrimidin-4-yl)-amine
 
−
* (5-Cyclopropyl-2H-pyrazol-3-yl)-[2-(3-methylphenylamino)-6-phenyl-pyrimidi- n-4-yl]-amine
 
−
* [2-(4-cyanomethylphenylamino)-6-phenyl-pyrimidin-4-yl]-(5-cyclopropyl-2H-p- yrazol-3-yl)-amine
 
−
* (5-Cyclopropyl-2H-pyrazol-3-yl)-[6-phenyl-2-(pyridin-3-ylmethylamino)-pyri- midin-4-yl]-amine
 
−
* [2-(3-Chlorophenyl)amino-6-(3-nitrophenyl)-pyrimidin-4-yl]-(5-methyl-2H-py- razol-3-yl)-amine
 
−
* [2-(3-Chlorophenyl)amino-6-(3,4,5-trimethoxyphenyl)-pyrimidin-4-yl]-(5-met- hyl-2H-pyrazol-3-yl)-amine
 
−
* (5-Methyl-2H-pyrazol-3-yl)-[2-(4-sulfamoylphenylamino)-6-(3,4,5-trimethoxy- phenyl)-pyrimidin-4-yl]-amine
 
−
* [2-(4-Chlorophenyl)amino-6-methyl-pyrimidin-4-yl]-[5-(furan-2-yl)-2H-pyraz- ol-3-yl]-amine
 
−
* [2-(Benzimidazol-2-ylamino-)6-ethyl-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3- -yl)-amine
 
−
* [2-(4-Chlorophenyl)amino-6-methyl-pyrimidin-4-yl]-(5-phenyl-2H-pyrazol-3-y- l)-amine
 
−
* [2-(4-Chlorophenyl)amino-6-ethyl-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl- )-amine
 
−
* (5-tert-Butyl-2H-pyrazol-3-yl)-[2-(3-chlorophenyl)amino-6-(3-nitrophenyl)-- pyrimidin-4-yl]-amine
 
−
* [2-(3-Chlorophenyl)amino-6-(3-nitrophenyl)-pyrimidin-4-yl]-(5-phenyl-2H-py- razol-3-yl)-amine
 
−
* [5-(Furan-2-yl)-2H-pyrazol-3-yl]-(6-phenyl-2-phenylamino-pyrimidin-4-yl)-a- mine
 
−
* [2-(Benzimidazol-2-ylamino)-6-methyl-pyrimidin-4-yl]-(5-phenyl-2H-pyrazol-- 3-yl)-amine
 
−
* [2-(Benzimidazol-2-ylamino)-6-methyl-pyrimidin-4-yl]-[5-(Furan-2-yl)-2H-py- razol-3-yl]-amine
 
−
* [2-(4-Chlorophenylamino)-6-methyl-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-y- l)-amine
 
−
* [2-(4-Chlorophenyl)amino-5,6-dimethyl-pyrimidin-4-yl]-(5-methyl-2H-pyrazol- -3-yl)-amine
 
−
* (5,6-Dimethyl-2-phenylamino-pyrimidin-4-yl)-(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Chlorophenyl)amino-6-methoxymethyl-pyrimidin-4-yl]-(5-methyl-2H-pyra- zol-3-yl)-amine
 
−
* [2-(Benzimidazol-2-ylamino)-6-methoxymethyl-pyrimidin-4-yl]-(5-methyl-2H-p- yrazol-3-yl)-amine
 
−
* (6-Methoxymethyl-2-phenylamino-pyrimidin-4-yl)-(5-methyl-2H-pyrazol-3-yl)-- amine
 
−
* (6-Methyl-2-phenylamino-pyrimidin-4-yl)-(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(2-Chlorophenoxymethyl)-6-methyl-pyrimidin-4-yl]-(5-phenyl-2H-pyrazol-3- -yl)-amine
 
−
* [2-(2-Chlorophenoxymethyl)-6-methyl-pyrimidin-4-yl]-[5-(furan-2-yl)-2H-pyr- azol-3-yl]-amine
 
−
* (6-methyl-2-phenoxymethyl-pyrimidin-4-yl)-(5-phenyl-2H-pyrazol-3-yl)-amine
 
−
* [5-(Furan-2-yl)-2H-pyrazol-3-yl]-(6-methyl-2-phenoxymethyl-pyrimidin-4-yl)- -amine
 
−
* [5-(Furan-2-yl)-2H-pyrazol-3-yl]-(6-methyl-2-phenylsulfanylmethyl-pyrimidin-4-yl)-amine
 
−
* [6-Methyl-2-(4-methyl-phenylsulfanylmethyl)-pyrimidin-4-yl]-(5-phenyl-2H-p- yrazol-3-yl)-amine
 
−
* [5-(Furan-2-yl)-2H-pyrazol-3-yl]-[6-Methyl-2-(4-methyl-phenylsulfanylmethy- l)-pyrimidin-4-yl]-amine
 
−
* [2-(4-Fluoro-phenoxymethyl)-6-methyl-pyrimidin-4-yl]-(5-phenyl-2H-pyrazol-- 3-yl)-amine
 
−
* [2-(4-Fluoro-phenoxymethyl)-6-methyl-pyrimidin-4-yl]-[5-(furan-2-yl)-2H-py- razol-3-yl]-amine
 
−
* (6-Ethyl-2-phenylsulfanylmethyl-pyrimidin-4-yl)-(5-methyl-2H-pyrazol-3-yl)- -amine
 
−
* (6-Ethyl-2-phenoxymethyl-pyrimidin-4-yl)-(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [6-Ethyl-2-(4-fluorophenoxymethyl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-- yl)-amine
 
−
* [6-Ethyl-2-(1-methyl-1-phenyl-ethyl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-- 3-yl)-amine
 
−
* [2-(4-Chlororophenoxymethyl)-6-methyl-pyrimidin-4-yl]-(5-phenyl-2H-pyrazol- -3-yl)-amine
 
−
* [2-(4-Chlororophenoxymethyl)-6-methyl-pyrimidin-4-yl]-(5-methyl-2H-pyrazol- -3-yl)-amine
 
−
* [2-(4-Chlororophenoxymethyl)-6-methoxymethyl-pyrimidin-4-yl]-(5-methyl-2H-- pyrazol-3-yl)-amine
 
−
* [2-(4-Chlororophenoxymethyl)-6-methyl-pyrimidin-4-yl]-[5-(furan-2-yl)-2H-p- yrazol-3-yl]-amine
 
−
* (5-Methyl-2H-pyrazol-3-yl)-(2-phenylsulfanylmethyl-5,6,7,8-tetrahydro-quin- azolin-4-yl)-amine
 
−
* [2-(4-Methylphenylsulfanylmethyl)-6,7,8,9-tetrahydro-5H-cycloheptapyrimidi- n-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(1-Methyl-1-phenyl-ethyl)-6,7,8,9-tetrahydro-5H-cycloheptapyrimidin-4-y- l]-(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(2,6-Dichlorobenzyl)-5,6,7,8-tetrahydro-quinazolin-4-yl]-(5-methyl-2H-p- yrazol-3-yl)-amine
 
−
* [7-Benzyl-2-(2,6-dichlorobenzyl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-- 4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [6-Benzyl-2-(4-chlorophenoxymethyl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimi- din-4-yl]-(5-methyl-2H-pyrazol-3-yl)-
 
−
* [2-(4-Chlorophenoxymethyl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-yl]- -(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(2,6-Dichlorobenzyl)-6-methyl-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl- )-amine
 
−
* [2-(2,6-Dichlorobenzyl)-5,6-dimethyl-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-- 3-yl)-amine
 
−
----
 
 
'''Patent Number''': US7008948  
 
'''Patent Number''': US7008948  
 
'''Applicant''': Vertex Pharmaceuticals Incorporated
 
'''Applicant''': Vertex Pharmaceuticals Incorporated
 
'''Title''': Fused pyrimidyl pyrazole compounds useful as protein kinase inhibitors
 
'''Title''': Fused pyrimidyl pyrazole compounds useful as protein kinase inhibitors
 +
 
'''Basic Structure'''
 
'''Basic Structure'''
  
 
[[Image:pyrazol2.jpeg]]
 
[[Image:pyrazol2.jpeg]]
  
−
'''Derivatives of pyrimidine-pyrazole amine disclosed in the patent:'''
+
[[Derivatives of pyrimidine-pyrazole amine disclosed in US7008948 patent]]
  
−
* [2-(2-Clorophenyl)-5,6-dimethylpyrimidin-4-yl]-(5-Methyl-2H-pyrazol-3-yl)-- amine
 
−
* [2-(2-Chloro-phenyl)-6,7,8,9-tetrahydro-5H-cycloheptapyrimidin-4-yl]-(1H-i- ndazol-3-yl)-amine
 
−
* (5-Fluoro-1H-indazol-3-yl)-[2-(2-trifluoromethyl-phenyl)-5,6,7,8-tetrahydr- o-pyrido[3,4-d]pyrimidin-4-yl]-
 
−
* [2-(2-Chloro-phenyl)-6,7,8,9-tetrahydro-5H-cycloheptapyrimidin-4-yl]-(7-fl- uoro-1H-indazol-3-yl)-amine
 
−
* [2-(2-Chloro-phenyl)-6,7,8,9-tetrahydro-5H-cycloheptapyrimidin-4-yl]-(5-fl- uoro-1H-indazol-3-yl)-amine
 
−
* [2-(2-Chloro-phenyl)-6,7,8,9-tetrahydro-5H-cycloheptapyrimidin-4-yl]-(5,7-- difluoro-1H-indazol-3-yl)-amine
 
−
* (7-Fluoro-1H-indazol-3-yl)-[2-(2-trifluoromethyl-phenyl)-5,6,7,8-tetrahydr- oquinazolin-4-yl]-amine
 
−
* (5-Fluoro-1H-indazol-3-yl)-[2-(2-trifluoromethyl-phenyl)-5,6,7,8-tetrahydr- oquinazolin-4-yl]-amine
 
−
* (5,7-Difluoro-1H-indazol-3-yl)-[2-(2-trifluoromethyl-phenyl)-5,6,7,8-tetra- hydroquinazolin-4-yl]-amine
 
−
* (5-Trifluoromethyl-1H-indazol-3-yl)-[2-(2-trifluoromethyl-phenyl)-5,6,7,8-- tetrahydroquinazolin-4-yl]-amine
 
−
* (5,7-difluoro-1H-indazol-3-yl)-[2-(2-trifluoromethyl-phenyl)-6,7,8,9-tetra- hydro-5H-cycloheptapyrimidin-4-yl]-amine
 
−
* (6-Benzyl-2-(2-trifluoromethyl-phenyl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyr- imidin-4-yl)-(5-fluoro-1H-indazol-3-yl)-amine
 
−
* (1H-Indazol-3-yl)-[2-(2-trifluoromethyl-phenyl)-6,7,8,9-tetrahydro-5H-cycl- oheptapyrimidin-4-yl]-amine
 
−
* (7-Fluoro-1H-indazol-3-yl)-[2-(2-trifluoromethyl-phenyl)-6,7,8,9-tetrahydr- o-5H-cycloheptapyrimidin-4-yl]-amine
 
−
* (5-Fluoro-1H-indazol-3-yl)-[2-(2-trifluoromethyl-phenyl)-6,7,8,9-tetrahydr- o-5H-cycloheptapyrimidin-4-yl]-amine
 
−
* (5-Fluoro-1H-indazol-3-yl)-[2-(2-trifluoromethyl-phenyl)-5,6,7,8-tetrahydr- o-pyrido[4,3-d]pyrimidin-4-yl]-amine
 
−
* (1H-indazol-3-yl)-[2-(2-trifluoromethyl-phenyl)-5,6,7,8-tetrahydroquinazol- in-4-yl]-amine
 
−
* (7-Benzyl-2-(2-trifluoromethyl-phenyl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-yl)-(5-fluoro-1H-indazol-3-yl)-amine
 
−
* (1H-Indazol-3-yl)-[6-methyl-2-(2-trifluoromethyl-phenyl)-pyrimidin-4-yl]-amine
 
−
* 1H-Indazol-3-yl)-[6-phenyl-2-(2-trifluoromethyl-phenyl)-pyrimidin-4-yl]-amine
 
−
----
 
 
'''Patent Number''': US6977262
 
'''Patent Number''': US6977262
 
'''Assignee''': Mitsubishi Pharma Corporation
 
'''Assignee''': Mitsubishi Pharma Corporation
 
'''Title''': Dihydropyrazolopyridine compounds and pharmaceutical use thereof
 
'''Title''': Dihydropyrazolopyridine compounds and pharmaceutical use thereof
 +
 
'''Basic Structure''':
 
'''Basic Structure''':
  
 
[[Image:pyrazol3.jpeg]]
 
[[Image:pyrazol3.jpeg]]
  
−
'''Derivatives of pyrimidine-pyrazole amine disclosed in the patent:'''
+
[[Derivatives of pyrimidine-pyrazole amine disclosed in US6977262 patent]]
  
−
* Ethyl 4-(2-chlorophenyl)-4,7-dihydro-6-methyl-2H-pyrazolo[3,4-b]pyridine-5-carboxylate
 
−
* Ethyl 4,7-dihydro-4-(2-methoxyphenyl)-6-methyl-2H-pyrazolo[3,4-b]pyridine-5-carboxylate
 
−
* Ethyl 4,7-dihydro-6-methyl-4-(2-trifluoromethylphenyl)-2H-pyrazolo[3,4-b]pyridin e-5-carboxylate
 
−
* Methyl 4-(2-chlorophenyl)-4,7-dihydro-6-methyl-2H-pyrazolo[3,4-b]pyridine-5-carboxylate
 
−
* t-Butyl 4-(2-chlorophenyl)-4,7-dihydro-6-methyl-2H-pyrazolo[3,4-b]pyridine-5-carboxylate
 
−
* Isopropyl 4-(2-fluorophenyl)-4,7-dihydro-6-methyl-2H-pyrazolo[3,4-b]pyridine-5-carboxylate
 
−
* Benzyl 4-(2-chlorophenyl)-4,7-dihydro-6-methyl-2H-pyrazolo[3,4-b]pyridine-5-carboxylate
 
−
* 4-(2-Chlorophenyl)-5-dimethylaminocarbonyl-4,7-dihydro-6-methyl-2H-pyrazolo [3,4-b]pyridine
 
−
* 4-(2-Chlorophenyl)-5-hydrazinocarbonyl-4,7-dihydro-6-methyl-2H-pyrazolo[3,4 -b]pyridine
 
−
* 4-(2-Fluorophenyl)-4,7-dihydro-6-methyl-5-isopropylthiocarbonyl-2H-pyrazolo [3,4-b]pyridine
 
−
* 4,7-Dihydro-6-methyl-5-nitro-4-(2-trifluoromethylphenyl)-2H-pyrazolo[3,4-b] pyridine
 
−
* Ethyl 4,7-dihydro-4-phenyl-6-trifluoromethyl-2H-pyrazolo[3,4-b]pyridine-5-carbox ylate
 
−
* Ethyl 4-(2-fluorophenyl)-4,7-dihydro-6-trifluoromethyl-2H-pyrazolo[3,4-b]pyridin e-5-carboxylate
 
−
* Ethyl 4-(2-chlorophenyl)-4,7-dihydro-6-trifluoromethyl-2H-pyrazolo[3,4-b]pyridin e-5-carboxylate maleate
 
−
* Ethyl 4,7-dihydro-4-(2-methoxyphenyl)-6-trifluoromethyl-2H-pyrazolo[3,4-b]pyridi ne-5-carboxylate
 
−
* Ethyl 4,7-dihydro-6-trifluoromethyl-4-(2-trifluoromethylphenyl)-2H-pyrazolo[3,4- b]pyridine-5-carboxylate
 
−
* Ethyl 4-(3-chlorophenyl)-4,7-dihydro-6-trifluoromethyl-2H-pyrazolo[3,4-b]pyridin e-5-carboxylate
 
 
----
 
----
 
'''Patent Number''': US6664247
 
'''Patent Number''': US6664247
 
'''Assignee''': Vertex Pharmaceuticals Incorporated
 
'''Assignee''': Vertex Pharmaceuticals Incorporated
 
'''Title''': Pyrazole compounds useful as protein kinase inhibitors'''
 
'''Title''': Pyrazole compounds useful as protein kinase inhibitors'''
 +
 
'''Basic Structure''':  
 
'''Basic Structure''':  
  
 
[[Image:pyrazol4.jpeg]]
 
[[Image:pyrazol4.jpeg]]
  
−
'''Derivatives of pyrimidine-pyrazole amine disclosed in the patent:'''
+
[[Derivatives of pyrimidine-pyrazole amine disclosed in US6664247 patent]]
  
−
* (5-Cyclopropyl-2H-pyrazol-3-yl)-[2-(naphtalen-2-ylsulfanyl)-6-phenylpyrimid in-4-yl]-amine
 
−
* 5-Cyclopropyl-2H-pyrazol-3-yl)-[2-(3-methoxycarbonyl-phenylylsulfanyl)-6-p henylpyrimidin-4-yl]-amine
 
−
* (5-Cyclopropyl-2H-pyrazol-3-yl)-[2-(naphthalen-2-ylsulfanyl)-pyrimidin-4-yl ]-amine
 
−
* (5-Cyclopropyl-2H-pyrazol-3-yl)-[5,6-dimethyl-2-(naphthalen-2-ylsulfanyl)-p yrimidin-4-yl]-amine
 
−
* (5-Cyclopropyl-2H-pyrazol-3-yl)-[5-methyl-2-(naphthalen-2-ylsulfanyl)-pyrim idin-4-yl]-amine
 
−
* (5-Cyclopropyl-2H-pyrazol-3-yl)-[6-methyl-2-(naphthalen-2-ylsulfanyl)-pyrim idin-4-yl]-amine
 
−
* (5-Cyclopropyl-2H-pyrazol-3-yl)-[6-(morpholin-4-yl)-2-(naphthalen-2-ylsulfa nyl)-pyrimidin-4-yl]-amine
 
−
* (5-Cyclopropyl-2H-pyrazol-3-yl)-[6-(1-methylpiperazin-4-yl)-2-(naphthalen-2 -ylsulfanyl)-pyrimidin-4-yl]-amine
 
−
* [6-(2,6-Dimethylphenyl)-2-(naphthalen-2-ylsulfanyl)-pyrimidin-4-yl]-(5-meth yl-2H-pyrazol-3-yl)-amine
 
−
* [6-(2-Methylphenyl)-2-(naphthalen-2-ylsulfanyl)-pyrimidin-4-yl]-(5-methyl-2 H-pyrazol-3-yl)-amine
 
−
* [2-(4-Acetamido-phenylsulfanyl)-6-phenyl-pyrimidin-4-yl]-(5-methyl-2H-pyraz ol-3-yl)-amine
 
−
* (5-Methyl-2H-pyrazol-3-yl)-[2-(naphthalen-2-ylsulfanyl)-6-phenyl-pyrimidin- 4-yl]-amine
 
−
* [2-(4-Isobutyrylylamino-phenylsulfanyl)-6-phenylpyrimidin-4-yl]-(5-methyl-2 H-pyrazol-3-yl)-amine
 
−
* [6-(4-Methylpiperazin-1-yl)-2-methylsulfanyl-pyrimidin-4-yl]-(5-methyl-2H-p yrazol-3-yl)-amine
 
−
* (5-Methyl-2H-pyrazol-3-yl)-[6-phenyl-2-(4-propionylamino-phenylsulfanyl)-py rimidin-4-yl]-amine
 
−
* [2-(4-Cyclopropanecarbonylamino-phenylsulfanyl)-6-phenylpyrimidin-4-yl]-(5- methyl-2H-pyrazol-3-yl)-amine
 
−
* (5-Methyl-2H-pyrazol-3-yl)-{6-phenyl-2-[4-(propane-1-sulfonylamino)-phenyls ulfanyl]-pyrimidin-4-yl}-amine
 
−
* [2-(4-Ethanesulfonylamino-phenylsulfanyl)-6-phenyl-pyrimidin-4-yl]-(5-methy l-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Acetamidophenyl-sulfanyl)-6-(2-methylphenyl)-pyrimidin-4-yl]-(5-methy l-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Isobutanecarbonylamino-phenyl-sulfanyl)-6-phenyl-pyrimidin-4-yl]-(5-m ethyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Acetamido-phenyl-sulfanyl)-5-methyl-6-phenyl-pyrimidin-4-yl]-(5-methy l-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Acetamido-phenyl-sulfanyl)-6-(4-methoxyphenyl)-pyrimidin-4-yl]-(5-met hyl-2H-pyrazol-3-yl)-amine
 
−
* [6-(3-Acetamidophenyl)-2-(4-acetamido-phenyl-sulfanyl)-pyrimidin-4-yl]-(5-m ethyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Isopropanesulfonylamino-phenyl-sulfanyl)-6-phenyl-pyrimidin-4-yl]-(5- methyl-2H-pyrazol-3-yl)-amine
 
−
* (2-[4-(2-Dimethylamino-acetylamino)-phenylsulfanyl]-6-phenyl-pyrimidin-4-yl }-(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(3-Chloro-benzylsulfanyl)-6-morpholin-4-yl-pyrimidin-4-yl]-(5-methyl-2H- pyrazol-3-yl)-amine
 
−
* [2-(3-Chloro-benzylsulfanyl)-6-(2-methoxy-ethylamino)-pyrimidin-4-yl]-(5-me thyl-2H-pyrazol-3-yl)-amine
 
−
* [2-Benzylsulfanyl-6-(4-methylpiperazin-1-yl)-pyrimidin-4-yl]-(5-methyl-2H-p yrazol-3-yl)-amine
 
−
* [2-Benzylsulfanyl-6-morpholin-4-yl-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-y l)-amine
 
−
* [2-(3-Chloro-benzylsulfanyl)-6-(4-methylpiperazin-1-yl)-pyrimidin-4-yl]-(5- methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-methoxy-benzylsulfanyl)-6-(4-methylpiperazin-1-yl)-pyrimidin-4-yl]-(5 -methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Acetamido-phenyl-sulfanyl)-6-tert-butyl-pyrimidin-4-yl]-(5-methyl-2H- pyrazol-3-yl)-amine
 
−
* 5-Cyclopropyl-2H-pyrazol-3-yl)-[6-phenyl-2-(4-propionylamino-phenyl-sulfan yl)-pyrimidin-4-yl]-amine
 
−
* [2-(3-Chloro-benzylsulfanyl)-6-(piperidin-1-yl)-pyrimidin-4-yl]-(5-methyl-2 H-pyrazol-3-yl)-amine
 
−
* (5-Methyl-2H-pyrazol-3-yl)-{2-[4-(morpholinesulfonyl)-benzylsulfanyl]-6-mor pholin-4-yl-pyrimidin-4-yl}-amine
 
−
* {6-(2-Methoxy-ethylamino)-2-[4-(morpholinesulfonyl)-benzylsulfanyl]-pyrimid in-4-yl}-(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* {6-(4-methylpiperazin-1-yl)-2-[4-(morpholinesulfonyl)-benzylsulfanyl]-pyrim idin-4-yl}-(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [6-Methoxymethyl-2-(4-propionylamino-phenyl-sulfanyl)-pyrimidin-4-yl]-(5-me thyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Methoxycarbonyl-phenyl-sulfanyl)-6-methoxymethyl-pyrimidin-4-yl]-(5-m ethyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(3,5-Dimethoxy-benzylsulfanyl)-6-morpholin-4-yl-pyrimidin-4-yl]-(5-methy l-2H-pyrazol-3-yl)-amine
 
−
* [2-(3,5-Dimethoxy-benzylsulfanyl)-6-pyrrolidin-4-yl-pyrimidin-4-yl]-(5-meth yl-2H-pyrazol-3-yl)-amine
 
−
* (5-Methyl-2H-pyrazol-3-yl)-[6-morpholin-4-yl-2-(naphthalene-2-yl-methylsulf anyl)-pyrimidin-4-yl]-amine
 
−
* {2-(4-Acetamido-phenyl-sulfanyl)-6-[4-(3-dimethylamino-propoxy)phenyl]-pyri midin-4-yl}-(5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Acetamidophenylsulfanyl)-6-(morpholin-4-yl)-pyrimidin-4-yl]-(5-methyl -2H-pyrazol-3-yl)-amine
 
−
* [6-Hydroxymethyl-2-(4-propionylamino-phenyl-sulfanyl)-pyrimidin-4-yl]-(5-me thyl-2H-pyrazol-3-yl)-amine
 
−
* [2-(4-Acetamido-phenyl-sulfanyl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl) -amine
 
−
* [6-(1-Butoxycarbonyl)-2-(4-propionylamino-phenyl-sulfanyl)pyrimidin-4-yl]-( 5-methyl-2H-pyrazol-3-yl)-amine
 
−
* [6-Methoxycarbonyl-2-(4-propionylamino-phenyl-sulfanyl)-pyrimidin-4-yl]-(5- methyl-2H-pyrazol-3-yl)-amine.
 
 
----
 
----
 
'''Patent Number''': US2004224944
 
'''Patent Number''': US2004224944
 
'''Assignee''': VERTEX PHARMACEUTICALS INC
 
'''Assignee''': VERTEX PHARMACEUTICALS INC
 
'''Title''': Pyrazole compounds useful as protein kinase inhibitors
 
'''Title''': Pyrazole compounds useful as protein kinase inhibitors
 +
 
'''Basic Structure''':  
 
'''Basic Structure''':  
  
 
[[Image:pyrazol5.jpeg]]
 
[[Image:pyrazol5.jpeg]]
  
−
'''Derivatives of pyrimidine-pyrazole amine disclosed in the patent:'''
+
[[Derivatives of pyrimidine-pyrazole amine disclosed in US2004224944 patent]]
−
 
+
−
* [2-(2-Chloro-phenyl)-6,7-dihydro-5H-cyclopentapyrimidin-4-yl]-(5,7-difluoro-1H-indazol-3-yl)-amine
+
−
* (1H-Indazol-3-yl)-[2-(2-trifluoromethyl-phenyl)-5,6,7,8,9,10-hexahydro-cyclooctapyrimidin-4-yl]-amine
+
−
* (7-Fluoro-1H-indazol-3-yl)-[2-(2-trifluoromethyl-phenyl)-5,6,7,8,9,10-hexahydro-cyclooctapyrimidin-4-yl]-amine
+
−
* (5,7-Difluoro-1H-indazol-3-yl)-[2-(2-trifluoromethyl-phenyl)-5,6,7,8,9,10-hexahydro-cyclooctapyrimidin-4-yl]-amine
+
−
* [6-Cyclohexyl-2-(2-trifluoromethyl-phenyl)-pyrimidin-4-yl]-(1H-indazol-3-yl)-amine
+
−
* [6-(2-Fluoro-phenyl)-2-(2-trifluoromethyl-phenyl)-pyrimidin-4-yl]-(1H-indazol-3-yl)-amine
+
−
* (6-Fluoro-1H-indazol-3-yl)-[2-(2-trifluoromethyl-phenyl)-quinazolin-4-yl]-amine
+
−
* 3-[2-(2-Trifluoromethyl-phenyl)-quinazolin-4-ylamino]-1H-indazole-5-carboxylic acid methyl ster
+
−
* (5-Methyl-2H-pyrazol-3-yl)-[2-(2-naphthyl-1-yl)-quinazolin-4-yl]-
+
−
* [2-(2-Chloro-phenyl)-pyrido[2,3-d]pyrimidin-4-yl]-(7-fluoro-1H-indazol-3-yl)-amine
+
−
* [2-(2-Chloro-phenyl)-pyrido[2,3-d]pyrimidin-4-yl]-(5-fluoro-1H-indazol-3-yl)-amine
+
−
 
+
−
=== Other derivates for alopecia ===
+
−
[[Image:other derivates.jpeg]]
+
−
 
+
−
== Inhibition of 5- - reductase by Finasteride ==
+
−
[[Image:5-alpha-reductase inhibition.jpeg]]
+
−
 
+
−
=== Structure-Activity Relationships(SARs) ===
+
−
[[Image:SAR_map.gif]]
+
−
 
+
−
== Questions Dolcera Answers ==
+
−
 
+
−
'''What’s hot?'''
+
−
* What compositions/ approaches are the most promising?
+
−
* What can I license?
+
−
* Can you map blockbuster products to their patents?
+
−
 
+
−
'''Can you save me some time?'''
+
−
* What combinations/ compounds have already been tried?
+
−
* Is any empirical data available?
+
−
* Can you tell me the side effects?
+
−
 
+
−
'''Where should I focus my R&D investment?'''
+
−
* What are the most promising approaches?
+
−
* Where’s the ‘white space’ for me to play in?
+
−
 
+
−
'''Any hints for research?'''
+
−
* Are there any combinations I could develop?
+
−
 
+
−
'''What should I do in this geography?'''
+
−
* What are my competitors up to in this geography?
+
−
* What are my strengths/ weaknesses here?
+
−
 
+
−
'''What’s my competition up to?'''
+
−
 
+
−
* What’s my top competitor investing in?
+
−
* Are there any loopholes in their patents?
+
−
* When are their patents expiring?
+
−
* Will a competitor emerge from nowhere and surprise me?
+
−
* What are the crowded areas?
+
−
 
+
−
'''How do I play defense?'''
+
−
* What should my blocking/reactive strategies be?
+
−
 
+
−
 
+
−
== New Combinations based on IP study? ==
+
−
 
+
−
Yes, new Combinations can be made with '''natural products''' based on IP study
+
−
* Walnut extract containing [[Image:5ar.jpg]] inhibitor (as anti-androgen) and Flavnones (for vasodilation).
+
−
* Sophora Flavnones (for vasodilation) in combination with Saw Palmetto berry (as anti-androgen).
+
−
 
+
−
'''Note:''' The above combinations are based on limited study and are only possible examples
+
−
 
+
−
== IP studies provides ==
+
−
 
+
−
=== Technology trends ===
+
−
* Use of saw palmetto berry for treating alopecia was first patented in 1996.
+
−
* Since then, 144 patents (including family patents) have been filed till 2006.
+
−
* Most patents use saw palmetto berry in combination with other products.
+
−
[[Image:Technology1.jpg|thumb|center|700px|Technology trends]]
+
−
 
+
−
=== New opportunities ===
+
−
Yes, the IP studies provide new opportunities in the following area.
+
−
* Sophora Flavescens contain flavnoids.
+
−
* Natural extract Sophora Flavescens cited in LG patent of 2001.
+
−
* Research shows fewer than 7 patents based on Sophora Flavescens for hair loss or alopecia.
+
  
−
* What's this?
+
[[Other derivates for alopecia]]
  
−
== GSK-3 Inhibition==
+
==== GSK-3 Inhibition Mechanism - Phosphorylation====
−
* ''GSK-3 inhibition targets treatment of chemotherapy-induced alopecia''[http://www.biomedcentral.com/1471-2199/5/15 source]
+
* ''GSK-3 inhibition targets treatment of chemotherapy-induced alopecia'' [http://www.biomedcentral.com/1471-2199/5/15 source]
 
* In the canonical Wnt signaling cascade, adenomatous polyposis coli (APC), axin, and GSK3 constitute the so-called destruction complex, which controls the stability of beta-catenin. It is generally believed that four conserved Ser/Thr residues in the N terminus of beta-catenin are the pivotal targets for the constitutively active serine kinase GSK3. GSK3 covalently modifies beta-catenin by attaching phosphate groups (from ATP) to serine, and threonine residues. In so doing, the functional properties of the protein kinase’s substrate (beta-catenin) are modified.  
 
* In the canonical Wnt signaling cascade, adenomatous polyposis coli (APC), axin, and GSK3 constitute the so-called destruction complex, which controls the stability of beta-catenin. It is generally believed that four conserved Ser/Thr residues in the N terminus of beta-catenin are the pivotal targets for the constitutively active serine kinase GSK3. GSK3 covalently modifies beta-catenin by attaching phosphate groups (from ATP) to serine, and threonine residues. In so doing, the functional properties of the protein kinase’s substrate (beta-catenin) are modified.  
  
Line 1,158: Line 813:
  
 
'''Serine - pyrazole reaction'''
 
'''Serine - pyrazole reaction'''
−
 
  
 
[[image:serine-pyrazol.jpg|600 px|center|thumb|Serine and Pyrazole reaction [http://www.genome.ad.jp/dbget-bin/www_bget?rn+R03134 source]]]
 
[[image:serine-pyrazol.jpg|600 px|center|thumb|Serine and Pyrazole reaction [http://www.genome.ad.jp/dbget-bin/www_bget?rn+R03134 source]]]
Line 1,187: Line 841:
 
'''Key Finding'''
 
'''Key Finding'''
 
* '''Pyrazole compounds with inhibition constant (Ki) of <0.1 mM''' are a good starting point for developing molecules that can inhibit serine/threonine protein kinase (such as GSK-3) and the proteins they help to regulate. [http://www.chemistry.org/portal/a/c/s/1/acsdisplay.html?DOC=patentwatch%5Carchive%5C011204_patentwatch.html source]
 
* '''Pyrazole compounds with inhibition constant (Ki) of <0.1 mM''' are a good starting point for developing molecules that can inhibit serine/threonine protein kinase (such as GSK-3) and the proteins they help to regulate. [http://www.chemistry.org/portal/a/c/s/1/acsdisplay.html?DOC=patentwatch%5Carchive%5C011204_patentwatch.html source]
 +
 +
=== Pathway associated with anti-androgen ===
 +
 +
* Dihydrotestosterone
 +
** Formed by peripheral conversion of testosterone by 5-alpha reductase
 +
** Binds to androgen receptor on susceptible hair follicles
 +
* Hormone-receptor complex activates genes responsible for gradual transformation of large terminal follicles to miniaturized (progressive diminution of hair shaft diameter and length in response to systemic androgens) follicles
 +
 +
[[Image:5-alpha-reductase inhibition.jpeg|center|500 px]]
 +
 +
==== Structure-Activity Relationships(SARs) ====
 +
[[Image:SAR_map.gif|center|720px]]
 +
 +
=== Pathway associated with Minoxidil (vasodilators) ===
 +
Minoxidil is a well know drug used for the treatment of alopecia. A co-relation between Sesquiterpene lactone (Helenalin) produced from Arnica montana and Minoxidil is illustrated in the figure below. Arnica montana, a Vasodilator, acts on  the NO/cGMP Pathway through T-cells, B-cells and epithelial cells & abrogates kappa B-driven gene expression.
 +
[[image:vasodiator-rev.jpg|800 px|center]]
 +
 +
== Alopecia IPMap ==
 +
[http://www.dolcera.com/client/d8r3/hairloss_map.htm Dolcera IPMap for Alopecia]
 +
 +
 +
 +
 +
 +
== Patent activity in China ==
 +
===Treatment approaches===
 +
{|border="2" cellspacing="0" cellpadding="4" width="100%"
 +
|align = "center"|'''Treatment approach'''
 +
|align = "center"|'''Patent number'''
 +
|align = "center"|'''Priority year'''
 +
|align = "center"|'''Assignee/Inventor'''
 +
|-
 +
|rowspan = "7"|Vasodilators
 +
|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN200510107497.8&leixin=fmzl&title=治疗瘀血阻滞型脱发的中草药汤剂及制备方法&ipc=A61K36/804(2006.01)I CN1772105]
 +
|2005
 +
|叶明伟
 +
|-
 +
|[http://v3.espacenet.com/textdoc?DB=EPODOC&IDX=CN1772139&F=0 CN1772139]
 +
|2005
 +
|王亚杰
 +
|-
 +
|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN03139861.8&leixin=fmzl&title=一种可用于治疗脱发、白发的天然中草药提取组合物及应用&ipc=A61K35/78 CN1569080]
 +
|2003
 +
|谈汝标
 +
|-
 +
|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN02155404.8&leixin=fmzl&title=毛囊激活液&ipc=A61K35/78 CN1506103]
 +
|2002
 +
|赵章光
 +
|-
 +
|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN01127395.X&leixin=fmzl&title=一种止脱生发药物及其制备方法&ipc=A61K35/78 CN1403100]
 +
|2001
 +
|范希田
 +
|-
 +
|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN96116925.7&leixin=fmzl&title=免洗养发生发香波&ipc=C11D3/48 CN1165181]
 +
|1996
 +
|殷国健
 +
|-
 +
|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN88103853.9&leixin=fmzl&title=一种通络生发香波&ipc=A61K7/06 CN1031022]
 +
|1988
 +
|天津市轻工业化学研究所
 +
|-
 +
|Hair matrix activator
 +
|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN02111941.4&leixin=fmzl&title=一种含中西药复方的育发剂&ipc=A61K7/06 CN1463693]
 +
|2002
 +
|朱静建
 +
|-
 +
|Anti-androgen <nowiki>+</nowiki> Vasodilator
 +
|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN96109964.X&leixin=fmzl&title=一种治疗脂溢性脱发的高效低副作用外用药物&ipc=A61K35/78 CN1150043]
 +
|1996
 +
|梅晓春
 +
|-
 +
|}
 +
 +
=== Details of treatment approaches===
 +
 +
{|border="2" cellspacing="0" cellpadding="4" width="100%" align="left"
 +
|align = "center"|'''Patent number'''
 +
|align = "center"|'''Patent title'''
 +
|align = "center"|'''Treatment approach'''
 +
|align = "center"|'''Composition nature'''
 +
|align = "center"|'''Composition'''
 +
|align = "center"|'''Composition action'''
 +
|-
 +
|align = "justify"|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN200510107497.8&leixin=fmzl&title=治疗瘀血阻滞型脱发的中草药汤剂及制备方法&ipc=A61K36/804(2006.01)I CN1772105]<br>YE MINGWEI (CN)<br>叶明伟 (2005)
 +
|align = "justify"|Chinese herbal medicine decoction for treating blood stasis obstruction type alopecia and its prepn<br>治疗瘀血阻滞型脱发的中草药汤剂及制备方法
 +
|align = "justify"|Vasodilators
 +
|align = "justify"|Herbal extract
 +
|align = "justify"|Astragalus root, prepared rhizome of rehmannia, white peony root, angelica, peach kernel and sufflower
 +
|align = "justify"|Promote blood circulation
 +
|-
 +
|align = "justify"|[http://v3.espacenet.com/textdoc?DB=EPODOC&IDX=CN1772139&F=0 CN1772139<br>]WANG YAJIE (CN)<br>王亚杰 2005
 +
|align = "justify"|Alopecia areata treating medicine<br>一种治疗斑秃的药物
 +
|align = "justify"|Vasodilators
 +
|align = "justify"|Herbal extract
 +
|align = "justify"|Pinellia tuber, fleeceflower root, arborvitae seed, chickení s gizzard membrane, prepared rhizome of rehmannia, Poris cocos, Codonopsis pilosula, etc
 +
|align = "justify"|Promote blood circulation
 +
|-
 +
|align = "justify"|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN03139861.8&leixin=fmzl&title=一种可用于治疗脱发、白发的天然中草药提取组合物及应用&ipc=A61K35/78 CN1569080]<br>TAN RUBIAO (CN)<br>谈汝标 2003
 +
|align = "justify"|Natural Chinese herb composition for treating alopecia and leucotrichia and its application<br>一种可用于治疗脱发、白发的天然中草药提取组合物及应用
 +
|align = "justify"|Vasodilators
 +
|align = "justify"|Herbal extract
 +
|align = "justify"|Ginger, Cinnamomum cassia, myrrh, clove, mace nutmeg, Loranthus mulberry mistletoe, rhizoma dioscoreae, ligustrum japonicum, drynaria, fleece-flower root, and black sesame seeds
 +
|align = "justify"|Enhances the hair growth and healthier hairs
 +
|-
 +
|align = "justify"|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN02111941.4&leixin=fmzl&title=一种含中西药复方的育发剂&ipc=A61K7/06 CN1463693]<br>朱静建 2002
 +
|Hair growing preparation containing compound of Chinese medicine and Western medicine<br>一种含中西药复方的育发剂
 +
|align = "justify"|Hair matrix activator
 +
|Mixture of Herbal extracts and western medicine
 +
|align = "justify"|Persimmon leaf, oriental arbor-vitae leaf, ginseng leaf, yellow qi, fruit of the glossy privet, polygonum multiflorum, Kudzu root, dry ginger; Plus：Minoxidil, Vitamins and derivative, cystine, serine, leucine.
 +
|align = "justify"|Better and  faster hair growth
 +
|-
 +
|align = "justify"|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN02155404.8&leixin=fmzl&title=毛囊激活液&ipc=A61K35/78 CN1506103]<br>赵章光2002
 +
|align = "justify"|Hair follice activating liquid<br>毛囊激活液
 +
|align = "justify"|Vasodilators
 +
|align = "justify"|Herbal extract
 +
|align = "justify"|Ginseng, twists the stock blue, the licorice, the Sophora flavescens and hot peppers
 +
|align = "justify"|Activates the hair-follicle and enhances the hair growth.
 +
|-
 +
|align = "justify"|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN01127395.X&leixin=fmzl&title=一种止脱生发药物及其制备方法&ipc=A61K35/78 CN1403100]<br>范希田 2001
 +
|align = "justify"|Trichogen and its prepn<br>一种止脱生发药物及其制备方法
 +
|align = "justify"|Vasodilators
 +
|align = "justify"|Herbal extract
 +
|align = "justify"|Ginseng, ganoderma lucidum, Chinese rhubarb, polygonum multiflorum, Chinese prickly ash, ginger, grass seed
 +
|align = "justify"|Promote blood circulation and enhance hair growth
 +
|-
 +
|align = "justify"|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN96116925.7&leixin=fmzl&title=免洗养发生发香波&ipc=C11D3/48 CN1165181]<br>殷国健 1996
 +
|Washing free shampoo for nourishing and growing hair<br>免洗养发生发香波
 +
|align = "justify"|Vasodilator
 +
|Vitamin composition
 +
|align = "justify"|Vitamin P (Bioflavonoids), Vitamin B15, Vitamin B2, nicotinic acid, bromo—geramineum
 +
|align = "justify"|Stimulate hair growth
 +
|-
 +
|align = "justify"|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN96109964.X&leixin=fmzl&title=一种治疗脂溢性脱发的高效低副作用外用药物&ipc=A61K35/78 CN1150043]<br>梅晓春 1996
 +
|Efficient low-side effect external use medicine for curing seborrheic baldness<br>一种治疗脂溢性脱发的高效低副作用外用药物
 +
|align = "justify"|Anti-androgen <nowiki>+</nowiki> Vasodilator
 +
|Mixture of Herbal extracts and organic compounds
 +
|align = "justify"|Polygonum multiflorum, Ligustrum lucidum, Morus alba, Rehmannia glutinosa, Eclipta prostrata, Saliva miltiorrhiza, Carthamus tinctorius, Cnidium monnieri, Sophora flavescens, Dictamnus dasycarpus, Kochia scoparia,  and antioxidants
 +
|align = "justify"|Inhibit the excess secretion of the sebaceous glands, increase the blood circulation on scalp and enhance the hair growth
 +
|-
 +
|align = "justify"|[http://search.sipo.gov.cn/sipo/zljs/hyjs-yx-new.jsp?recid=CN88103853.9&leixin=fmzl&title=一种通络生发香波&ipc=A61K7/06 CN1031022]<br>天津市轻工业化学研究所 1988
 +
|Channel-stimulating and hair-growing hair shampoo<br>一种通络生发香波
 +
|align = "justify"|Vasodilators
 +
|Herbal extract <nowiki>+</nowiki> detergent
 +
|align = "justify"|<font color="#454545">Herbal extracts, Penetration media, Detergents.</font>
 +
|align = "justify"|Increases the blood circulation under the scalp, reduces the hair los
 +
|-
 +
|}<br clear="all">
 +
 +
 +
==<span style="color:#C41E3A">Like this report?</span>==
 +
<p align="center"> '''This is only a sample report with brief analysis''' <br>
 +
'''Dolcera can provide a comprehensive report customized to your needs'''</p>
 +
{|border="2" cellspacing="0" cellpadding="4" align="center" "
 +
|style="background:lightgrey" align = "center"  colspan = "3"|'''[mailto:info@dolcera.com <span style="color:#0047AB">Buy the customized Alopecia report from Dolcera</span>]'''
 +
|-
 +
| align = "center"| [http://www.dolcera.com/website_prod/services/ip-patent-analytics-services Patent Analytics Services]
 +
|align = "center"| [http://www.dolcera.com/website_prod/services/business-research-services Market Research Services]
 +
|align = "center"| [http://www.dolcera.com/website_prod/tools/patent-dashboard Purchase Patent Dashboard]
 +
|-
 +
|align = "center"| [http://www.dolcera.com/website_prod/services/ip-patent-analytics-services/patent-search/patent-landscapes Patent Landscape Services]
 +
|align = "center"| [http://www.dolcera.com/website_prod/research-processes Dolcera Processes]
 +
|align = "center"| [http://www.dolcera.com/website_prod/industries Industry Focus]
 +
|-
 +
|align = "center"| [http://www.dolcera.com/website_prod/services/ip-patent-analytics-services/patent-search/patent-landscapes Patent Search Services]
 +
|align = "center"| [http://www.dolcera.com/website_prod/services/ip-patent-analytics-services/alerts-and-updates Patent Alerting Services]
 +
|align = "center"| [http://www.dolcera.com/website_prod/tools Dolcera Tools]
 +
|-
 +
|}
 +
<br>
  
 
== Conclusions ==
 
== Conclusions ==
Line 1,193: Line 1,016:
 
* The top companies are Merck, L’Oreal and Smithkline.
 
* The top companies are Merck, L’Oreal and Smithkline.
  
−
== Useful links ==
+
==Contact Dolcera==
−
* [http://www.biocarta.com/pathfiles/h_ghPathway.asp Pathways example]
+
−
* [http://www.cellsignal.com/category.asp?catalog_name=CellSignal&category_name=MAPK+Signaling Signaling Pathways]
+
  
−
== Summary ==
+
{| style="border:1px solid #AAA; background:#E9E9E9" align="center"
 +
|-
 +
! style="background:lightgrey" | Contact Dolcera
 +
|-
 +
| '''Email''': [mailto:info@dolcera.com info@dolcera.com]
 +
|-
 +
| '''Phone''': +1-650-269-7952
 +
|}

Latest revision as of 03:04, 4 December 2014

Contents

Rationale

  • "Medication for men plagued by hair loss has become a topic of interest in Japan since a drug company began marketing it at the end of last year." March 5th, 2006 – Source
  • "An increasing number of companies are apparently turning the Chinese fear of a bald spot into big bucks with some doing so well they are branching out into other countries." February 16, 2006 – Source
  • "There is something in the air, or should we say in the hair, these days. Scientific research into hair loss remedies has never been more active or more exciting." June 7, 2006 - Source


Introduction

Hair basics

  • Hair is a complex and delicate part of the body.
  • Keeping it healthy and beautiful is a challenge.
  • Hair grows everywhere on the body with the exception of lips, eyelids, palms of the hands and soles of the feet.
  • Hair is basically a form of skin.
  • Hair is made up of a protein called keratin.
  • Each shaft of hair is made of two or three inter-twined layers of keratin which grow from a follicle beneath the skin.
  • Hair Structure - Source
  • Hair Cycle - Source
Structure of Hair root and Hair bulb

What causes hair loss?

  • Decrease in growth of hair
  • Increase in shedding of hair
  • Breakage of hair
  • Conversion of thick terminal hairs to thin vellus hairs
Survey results from Japan

Both men and women lose hair for similar reasons. Hair loss in men is often more dramatic, and follows a specific pattern of loss, one of which has been termed “Male Pattern Baldness" or "Androgenetic Alopecia".


Types of alopecia

  • Alopecia Areata (AA): Hair loss occurring in patches anywhere on the body.
  • Alopecia Totalis (AT): Total loss of the hair on the scalp.
  • Alopecia Universalis (AU): Total loss of all hair on the body.
  • Alopecia Barbae: Loss of facial hair (for a man) especially in the beard area.
  • Alopecia Mucinosa: A type of alopecia which results in scaley patches.
  • Androgenetic Alopecia (AGA): Also known as male pattern baldness. It is a thinning of the hair to an almost transparent state, in both men or women. It is thought to be a hereditary form of hair loss.
  • Traction Alopecia: Traction alopecia is usually due to excessive pulling or tension on hair shafts as a result of certain hair styles. It is seen more often in women, particularly those of East Indian and Afro-Caribbean origin. Hair loss depends on the way the hair is being pulled. Prolonged traction alopecia can stop new hair follicles from developing and leads to permanent hair loss.
  • Anagen Effluvium: This hair loss is generally caused by chemicals such as those used to treat cancer. Initially it causes patchy hair loss, which often then leads to total hair loss. The good news is that when you stop using these chemicals the hair normally grows back (usually about 6 months later). Other drugs also can cause hair loss. Many medicines used to treat even common diseases can cause hair loss.
  • Scarring Alopecia: A form of alopecia which leaves scarring on the area of hair loss.
  • Telogen Effluvium: A form of hair loss where more than normal numbers of hair fall out. There is a general 'thinning' of the hair. Unlike some other hair and scalp conditions, it is temporary and the hair growth usually recovers. (Source)

Androgenetic alopecia

  • Gradual onset
  • Transition from large, thick, pigmented terminal hairs to thinner, shorter, indeterminate hairs and finally to short, wispy, non-pigmented vellus hairs in the involved areas
  • Characterized by a receding hairline and/or hair loss on the top of the head

Main causes

  • Genetic predisposition
  • Hormonal effect of androgen
  • Reduction of blood circulation around hair follicle
  • Deactivation of hair matrix cells

Some facts from Japan

  • Market size: ¥ 30 Billion
  • Number of products: more than 100

(JICST-EPlus - Japanese Science & Technology)

IP activity over the years

The graph indicates:

  • Number of patents filed every 5 years (except for first 7 years).
  • First solution proposed in 1973
  • Filing trend indicates steep rise in activity recently.
IP Activity over years

Major players

Assignees with more than 20 patents
Assignees with fewer than 20 patents

  • Active assignees

Assignees currently active with more than 5 patents to their credit during 2000-2005.

  • Warner with 9 patents,
  • Bristol with 6 and
  • Abbott with 5.
Active Assignees

Taxonomy

Alopecia toxonomy.jpg

Interactive Taxonomy

Use the mouse(click and drag/scroll up or down/click on nodes) to explore nodes in the detailed taxonomy
Click on the red arrow on the side of a node name to view the content for that particular node in the dashboard

Treatment Approaches

Composition of treatment for causes are identified and categorized as follows:

  • Anti-androgens (Finasteride) source
  • Vasodilators (Minoxidil) source
  • Double action (Anti-androgen + Vasodilator)
  • Hair matrix cells activator
Cause Treatment approach Pathways affected
Hormonal effect of androgen Anti-androgens Testosterone pathway
Reduction of blood circulation around hair follicle Vasodilators (eg. Minoxidil) NO/cGMP Pathway
Deactivation of hair matrix cells Hair matrix cells activator
  • Wnt pathway
  • STAT pathway
  • TGF beta/BMP Pathway
  • FGF Pathway
  • MAPK Pathway
  • NOTCH Pathway
  • Hedgehog Pathway

Anti-androgens

  • Anti-androgens are used in hormone therapy.
  • Anti-androgens are designed to affect the hormones made in the adrenal glands. They don't stop the hormones from being made, but they stop them from having an effect leading to hair loss.

What causes hair loss?

  • Testosterone is reduced to its active metabolite, Dihydrotestosterone (DHT) by the enzyme 5 alpha reductase.
  • DHT attaches to androgen receptor sites at the hair follicle.
  • DHT causes gradual miniaturization of the follicle, which eventually results in hair loss.

How do anti-androgens treat hair loss?

  • Anti-androgens compete with DHT to bind to the androgen receptor.
  • Upon binding of anti-androgen in place of DHT, follicle miniaturization is lowered and hair loss prevented.

Functions of Anti-androgen

Anti-androgen

Functions of Anti-androgen

IP Map for anti-androgen

Pat/Pub# Nature Composition Composition action
US20060009430

BLOTECH (2004)

Natural extracts Palmetto berry extract (fatty acids & sterols), Pumpkin seed extract (Vitamins-B, alpha-linolenic acid, amino acids and phytosterols), Quercetin (Flavonoids) and Beta-sitosterol (Rice bran, wheat germ, corn oils and soybeans) Fatty acids – Inhibit testosterone

Sterols - Mechanism of action unknown.

Quercetin results in cell growth cycle.

Beta-sitosterol reduce inflammation on scalp

US20060009427

WARNER LAMBERT(2004)

Organic compound New class of 4-cycloalkoxy benzonitrile derivatives and salts Acts as androgen receptor modulator and blocks formation of DHT.
US20050085467

WARNER LAMBERT(2004)

Organic compound New class of 6-sulfonamido-quinolin-2-one and 6-sulfonamido-2-oxo-chromene derivatives. The compounds inhibit, or decrease, activation of androgen receptor by androgens.
US20050118282

APHIOS Corp (2003)

Natural extracts Supercritical fluid isolate of Saw Palmetto and Sperol (Serenoa repens berry) and their analogs or derivatives. Modulates androgenic activity by inhibiting 5.alpha.-reductase activity.
US20060009429

Fundacion Pablo Cassara (2003)

Nucleotide Pharmacologically active oligonucleotides (encompass both DNA and S-DNA bond) Oligonucleotides inhibit androgen receptor (AR) expression at very low concentrations in skin and hair follicle
US20030007941

PFIZER INC (2001)

Organic compound Thyromimetic compounds (structurally similar to thyronine) with finasteride, or cyproterone acetate Activates thyroid hormone receptors in hair follicle which in turn promote elasticisation of follicle walls and hair follicle
US20030073616

N/A (1995)

Peptides/nucleic acid Bradykinin antagonist (peptide of plasma origin from kininogen precursor-kallikrein) Inhibits synthesis of bradykinin receptors or compounds by binding to B2 receptor
EP0279010

KAO Corp (1987)

Natural extracts Walnut extract (leaves/pericarps) with an organic solvent Blocks formation of DHT

Minoxidil (Vasodilators)

  • Minoxidil is a "potassium channel opener" that leads to vasodilation.
  • The drug is available in two forms. Oral minoxidil is used to treat high blood pressure and the topical solution form is used to treat hair loss and baldness.

What causes hair loss?

  • A thick network of tiny veins and arteries line the outer wall of the follicle. Blood pumps through the bulb and hair via this network.
  • DHT accumulates in the hair follicles and roots, constricting the blood supply of oxygen and nutrients to the hair roots; which is also seen to possibly contribute towards hair loss.

How does Minoxidil treat hair loss?

  • Minoxidil is applied to the scalp topically, where it dilates blood vessels in the scalp and sustains the hair follicles for longer period of time.
  • Minoxidil is thought to have a direct mitogenic effect on epidermal cells, as has been observed both in vitro and in vivo. Though the mechanism of its action for causing cell proliferation is not very clear, minoxidil is thought to prevent intracellular calcium entry. Calcium normally enhances epidermal growth factors to inhibit hair growth, and Minoxidil by getting converted to minoxidil sulfate acts as a potassium channel agonist and enhances potassium ion permeability to prevent calcium ions from entering into cells. (Source)
  • Minoxidil sulfate (MS) appears to be the active metabolite responsible for hair growth stimulation.

Functions of Vasodilators

Functions of Monoxidil source

IP Map for Vasodilators

Pat/Pub# Nature Composition Composition action
US20040157856

WARNER LAMBERT(2002)

Organic compound Benzopyran compounds Rapidly metabolizes, and causes reduced cardiovascular effects as compared to other known potassium channel openers
US20050053572

LG HOUSEHOLD & HEALTH CARE(2001)

Natural extracts Sophora flavescens extract (alkaloids & flavonoids, luteolin-7-glucose and cytosine) Hinokitiol (Taiwan hinoki oil, Aomori, Western Red Cedar oil) and Nicotinamide (Vitamin B complex) Promotes function of cell activity and dilates blood vessels

Double action (Anti-androgen + Vasodilator)

  • Combination of Vasodilator + Anti-androgen (double action) composition for effective treatment of Male-Pattern Baldness.

What is the problem with using only Anti-androgen therapy?

  • Anti-androgen is not effective in addressing the issue of vasocontriction around hair follicles due to sebum oil build up.
  • Anti-androgen only prevents binding of DHT to androgen receptors. However, the effects of improper oxygen and nutrient supply to the brain due to vasocontriction still remains and gradually causes hair loss.

What is the problem with using only Vasodilator (or Minoxidil only) therapy?

  • Vasodilator or Minoxidil-based products are generally not effective in stopping hair loss as vasodilators (or Minoxidil) do not block the harmful effects of DHT in the scalp and hair follicles.
  • Vasodilators or Minoxidil simply dilate blood vessels in the scalp. However, the harmful DHT still gets produced in the body, enters the scalp and hair follicles causing hair loss.

How is the combination of Anti-androgens and Vasodilator (or Minoxidil) effective?

  • Anti-androgens target the problem of DHT binding to androgen receptors and prevents follicle miniaturization.
  • Vasodilators like Minoxidil cause vasodilation and therefore improve supply of oxygen and nutrients to the hair follicle and roots.
  • Combination therapy therefore proves to be much more effective than individual therapy.

Functions of (Anti-androgen + Vasodilators)

Anti-androgen and Minoxidil

Functions of (Anti-androgen + Vasodilators)

IP Map for (Anti-androgen + Vasodilators)

Pat/Pub# Nature Composition Composition action
US20060052405

N/A(2000)

Peptides Testosterone blocker or vascular toner (Flutamide, cyproterone acetate, spironolactone, progesterone, or analogs or derivatives) and minoxidil mixed along with non-retinoid penetration enhancer and sunscreen Inhibits 5.alpha.-reductase activity (block DHT) and increase blood flow on the scalp
US20050123577

L'OREAL(2000)

Peptides Prostaglandin (polyunsaturated fatty acids) EP-2, EP-3 EP-4 receptor agonist with Minoxidil, 2,4-diaminopyrimidine 3-oxide, and Aminexil, cyclic AMP Minoxidil (designed to mimic nitric oxide's effects) grows hair via prostaglandin-H synthase stimulation. EP-3 and EP-4 are expressed in anagen hair follicles which induce a reduction in the level of cAMP
US6447762

COLOMER GROUP(1999)

Natural extract Hop extract (oil contains terpenes and humulene), Rosemary extract (hydroalcohol), Swertia extract (glycol with a swertiamarin), Silanodiol salicylate (biologically active silicon compound) Inhibits activity of 5-alpha-reductase, protects follicular cell membranes by neutralizing action of oxidation reaction in tissues, stimulates hair follicles and blood circulation to the hair root, supplies oxygen and nutrients to base of follicle, retains humidity, avoids dehydration of scalp

Hair matrix cell activator

Hair matrix cell activator is a substance that acts at the matrix cells in the hair follicle preventing their degradation.

What causes hair loss?

  • Stem cells are interspersed within the basal layer of the outer root sheath and in an area called the bulge.
  • Stem cells migrate to hair matrix where they start to divide and differentiate, under the influence of substances produced by cells of the dermal papilla.
  • Perifollicular matrix cells undergo slow degradation which prevents follicle stimulation.
  • Hair follicle activation is required for hair growth and thus inhibition of follicle activation eventually leads to hair loss.


How does hair cell matrix activator treat hair loss?

  • Hair cell matrix activator slows down and inhibits degradation of the perifollicular matrix.
  • This leads to an increase in hair follicle matrix cells that differentiate from progenitor stem cells.
  • Matrix activator allows activation of hair matrix cells and therefore follicle stimulation leading to hair growth.

Functions of Hair matrix cell activator

Hair matrix cell activator

Functions of Hair matrix cell activator

IP Map for Hair matrix cell activator

Pat/Pub# Nature Composition Composition action
US20020052498

SHISEIDO(1999)

Organic compound (2-substituted oxyphenyl) alkanamide derivative and its salt Mechanism of action has not been made clear, having excellent hair follicle activating action and regrowth promoting effect
US20040071647

L'OREAL(1998)

Peptides Metalloprotease (MMP-9) inhibitor (thiol or a hydroxamate) other than chelating calcium ions Reducing the expression of MMPs (Metalloproteases) in the scalp - slows down or inhibits the degradation of the perifollicular matrix (extracellular matrix surrounding the hair follicle)

Technology mapping based on patents analyzed

IPMap: Composition nature matrix

Year Organic Compound Natural extracts Peptides Nucleotides Natural extract + Organic comp
2005 .... .... .... .... UNILEVER (1)
2004 WARNER (1) BLOTECH (1) .... .... KAO (1)
2003 WARNER (1) APHIOS (1) .... FUNDACION (1) ....
2002 WARNER (1) .... .... .... ....
2001 PFIZER (1) LG HEALTH-CARE (1) .... .... ....
2000 .... .... L’OREAL (1) / N/A (1) .... ....
1999 SHISEDIO (1) COLOMER (1) .... .... ....
1998 .... .... L’OREAL (1) .... ....
1995 .... .... N/A (1) .... ....
1987 .... KAO (1) .... .... ....
1982 UNILEVER (1) .... .... .... ....

Focus of patents

Focus of patents Patent no. Rec. no.
2-substituted oxyphenyl alkanamide derivative having excellent hair growth effect. US20020052498 1
Thyromimetic compounds, and its role in treating hair loss US20030007941 2
Saw Palmetto berry extract, pumpkin seed extract, sitosterol and quercetin for the treatment and prevention of the biologically detrimental effects of DHT US20060009430 3
4-cycloalkoxy benzonitriles and its use as androgen receptor modulators US20060009427 4
Supercritical fluid isolate of Saw Palmetto, Sperol for inhibition of 5-.alpha.-reductase activity US20050118282 5
New class of quinolin-2-ones and chromen-2-ones andtheir use as androgen receptor antagonists US20050085467 6
Antiandrogen oligonucleotides usable for the treatment of dermatological androgen-related disorders US20060009429 7
Bradykinin antagonists for stimulating or inducing hair growth and/or arresting hair loss US20030073616 8
Extract from walnut leaves and/or pericarps as 5 alpha -reductase inhibitor EP0279010 9
Stimulating hair growth using benzopyrans US20040157856 10
Sophora flavescens extract, Coicis semen extract, clove extract, etc for promoting hair growth, function of cell activity and dilating peripheral blood vessels. US20050053572 11
Compositions to prevent or reduce hair loss US20060052405 12
Prostaglandin EP-3 receptor antagonists for reducing hair loss US20050123577 13
Synergic effect arising from the interaction of active ingredients, consisting of three plant extracts and a synthetic organosilicic compound for prevent hair loss and stimulate hair growth US6447762 14
Metalloprotease inhibitors to induce and/or stimulate the growth US20040071647 15
Method of decreasing sebum production and pore size US20050277699 16
Method for reducing sebum on the hair and skin US4529587 17

Technology focus

Technology focus

Distribution of patents

By patent types

Distribution based on patent types


By key ingredients

Distribution of key ingredients

By target disease

Distribution based on target diseases


Key ingredients vs. Target disease

Key ingredients vs. Target disease


Target species

Target species


Mode of administration

Mode of administration


Product type vs. Product form

Product type vs. Product form

Patents by target diseases

Target disease/ disorder Patent no. Rec. no.
Alopecia areata, alopecia pityrodes or alopecia seborrheica, or androgenic alopecia (i.e. male pattern baldness) US20020052498 1
Alopecia areata, male pattern baldness and female pattern baldness US20030007941 2
Androgenic alopecia (i.e. male pattern baldness), prostatic hyperplasia or both. US20060009430 3
Inappropriate activation of the androgen receptor, acne, oily skin, alopecia US20060009427 4
Prostatic hyperplasia, prostatic cancer, hirsutism, acne, male pattern baldness, seborrhea, and other diseases related to androgen hyperactivity US20050118282 5
Alopecia, acne, oily skin, prostrate cancer, hirsutism, and benign prostate hyperplasia US20050085467 6
Androgen-associated hair loss and androgen-skin related disorders. US20060009429 7
Androgenetic or androgenic alopecia or androgeno-genetic alopecia US20030073616 8
Diseases caused by testosterone (male-pattern alopecia) EP0279010 9
Alopecia areata, female pattern hair loss, hair loss secondary to chemotherapy or radiation treatment, stress-related hair loss, self-induced hair loss, scarring alopecia, and alopecia in non-human mammal US20040157856 10
Male pattern alopecia US20050053572 11
Alopecia, androgenic alopecia US20060052405 12
Hair loss US20050123577 13
Male pattern alopecia US6447762 14
Androgenetic, androgenic or androgenogenetic alopecia US20040071647 15
Curing other scalp related problems US20050244362 16


List of patents

Pathways and linkages

Pathways associated with hair matrix cell activation

Molecular mediators of hair follicle embryogenesis: Identification of the molecular pathways controlling differentiation and proliferation in mammalian hair follicles provides the crucial link to understanding the regulation of normal hair growth, the basis of hereditary hair loss diseases, and the origin of follicle-based tumors. Homeobox (hox), hedgehog (hh), patched (ptc), wingless (wg}/wnt, disheveled (dsh), engrailed (en), Notch 1 and armadillo/B-catenin genes are all critical for hair follicle.

  • Wnt pathway: Maintains hair-inducing activity of the dermal papilla.
  • Hedgehog pathway: Sonic hedgehog (SHH) signaling plays a critical role in hair follicle development. Sonic hedgehog gene. Sonic hedgehog, SHH for short, helps guide hair follicles from a resting stage into growth activity. SHH is particularly important in the embryonic formation of hair follicles.
  • STAT pathway
  • TGF beta/BMP Pathway: Bone morphogenetic protein (BMP) signaling have been implicated in the regulation of both proliferation and differentiation in the hair follicle. BMP2 is expressed in the embryonic ectoderm, but then localizes to the early hair follicle placode and underlying mesenchyme. BMP4 is expressed in the early dermal condensate. Research results show that BMPs are a key component of the signaling network controlling hair development and are required to induce the genetic program regulating hair shaft differentiation in the anagen hair follicle. Transforming growth factor beta (TGF-beta), inhibits mitogen - induced dermal papilla cell proliferation
  • FGF Pathway: Fibroblast growth factor (bFGF) and platelet-derived growth factor (PDGF) potentiate the growth of dermal papilla cells. It is proposed that these proteins increase the synthesis of stromelysin (an enzyme, matrix metalloproteinase) which acts on the papilla cells and accelerates their growth.
  • MAPK Pathway: Mitogen-activated protein kinase (MAPK) activation, increases keratinocyte turnover.
  • NOTCH Pathway: Notch-1 is expressed in ectodermal-derived cells of the follicle, in the inner cells of the embryonic placode and the follicle bulb, and in the suprabasal cells of the mature outer root sheath. Delta-1, one of the three ligands is only expressed during embryonic follicle development and is exclusive to the mesenchymal cells of the pre-papilla located beneath the follicle placode, and appears to promote and accelerate placode formation, while suppressing placode formation in surrounding cells. Other ligands, Serrate 1 and Serrate 2, are expressed in matrix cells destined to form the inner root sheath and hair shaft.

Pathways associated with Anti Androgen

Alopecia pathways

Players of WNT inhibition Pathway

Wnt inhibition
Patent no. Key compound Players of inhibition
US6664247 Pyrazole compounds GSK3
US6989385 Pyrazole compounds GSK3
WO2005012256 Pyrazole compounds CDK,GSK3
US6974819 Pyrimidine derivative GSK3
US6743791 Heterocyclic compounds AKT3, GSK-3, ERK2
US20050277773 Pyrrolo[3,2-d]pyrimidine derivatives GSK3
US20040072836 Aza-oxindole derivatives GSK3, AKT, PKC
EP1477489 Pyrrolopyrimidine derivatives GSK3
WO0056710 3-(Anilinomethylene) oxindoles GSK3, AKT, PKC
WO2003011287 Pyrazolon derivatives GSK3, ß-catenin
US6924141 Lithium chloride, Wnt3/4/ 7 ß-catenin, GSK3, Wnt
US6706685 Peptide sequence ß-catenin
US6683048 Peptide sequence a-catenin, ß-catenin
US6677116 Peptide sequence LXXLL ß-catenin
US6303576 Peptide sequence LXXLL ß-catenin

Role of Pyrazole compounds in Wnt Pathway

Pyrazole

  • Pyrazole (C3H4N2) refers both to the class of simple aromatic ring organic compounds of the heterocyclic series characterized by a 5-membered ring structure composed of three carbon atoms and two nitrogen atoms in adjacent positions and to the unsubstituted parent compound. Being so composed and having pharmacological effects on humans, they are classified as alkaloids although they are not known to occur in nature.
  • Pyrazoles are produced synthetically through the reaction of a,ß-unsaturated aldehydes with hydrazine and subsequent dehydrogenation
Pyrazole (C3H4N2)
  • Pyrazoles are used for their analgesic, anti-inflammatory, antipyretic, antiarrhythmic, tranquilizing, muscle relaxing, psychoanaleptic, anticonvulsant, monoamineoxidase inhibiting, antidiabetic and antibacterial activities.
  • Structurally related compounds are pyrazoline and pyrazolidine.
Structurally related compounds

GSK3 inhibition by pyrazole compounds

Bold3.jpg

US6989385

US6989385.jpg

US6664247

US6664247.jpg

WO2005012256

WO2005012256.jpg

R1=T-Ring D, wherein

T is a valence bond and Ring D = 5-6 membered aryl or heteroaryl ring;

R2 = hydrogen or C1-4 aliphatic and R2'= hydrogen;

R3 = -R, -OR, or -N(R4)2, wherein R = hydrogen, C1-6 aliphatic, 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl, and L is -O-, -S-, or -NH-; and Ring D is substituted by up to three substituents selected from -halo, -CN, -NO2, -N(R4)2, optionally substituted C1-6 aliphatic group, -OR, -C(O)R, -CO2R, -CONH(R<4>), -N(R4)COR, -N(R4)CO2R, -SO2N(R4)2, -N(R4)SO2R, -N(R6)COCH2N(R4)2, -N(R6)COCH2CH2N(R4)2, or -N(R6)COCH2CH2CH2N(R4)2, wherein R = hydrogen, C1-6 aliphatic, phenyl, 5-6 membered heteroaryl ring, or 5-6 membered heterocyclic ring

X = R1-A-NR4- or a 5- or 6-membered carbocyclic or heterocyclic ring; A is a bond, S02, C=O, NRg(C=O) or O(C=O) wherein Rg is hydrogen or C1-4 hydrocarbyl optionally substituted by hydroxy or C1-4 alkoxy; Y is a bond or an alkylene chain of 1, 2 or 3 carbon atoms in length;

R1 is hydrogen; carbocyclic or heterocyclic group having from 3 to 12 ring members; or C1-8 hydrocarbyl group optionally substituted by one or more substituents selected from halogen (e.g. fluorine), hydroxy, C1-4 hydrocarbyloxy, amino, mono- or di-C1-4 hydrocarbylamino, and carbocyclic or heterocyclic groups having from 3 to 12 ring members, and wherein 1 or 2 of the carbon atoms of the hydrocarbyl group may optionally be replaced by an atom or group selected from 0, S, NH, SO, S02;

R2 is hydrogen; halogen; C1-4 alkoxy (e.g. methoxy); or a C1-4 hydrocarbyl group optionally substituted by halogen (e.g. fluorine), hydroxyl or C1-4 alkoxy (e.g. methoxy); R3 is selected from hydrogen and carbocyclic and heterocyclic groups having from 3 to 12 ring members; and

R4 is hydrogen or a C1-4 hydrocarbyl group optionally substituted by halogen (e.g. fluorine), hydroxyl or C1-4 alkoxy (e.g. methoxy).

X is a groupR1-A-NR4-or a 5-or 6-membered carbocyclic or heterocyclic ring;

A is a bond,SO2, C=O, NRg (C=O) or O(C=O) wherein Rg is hydrogen orC14 hydrocarbyl optionally substituted by hydroxy or C1-4 alkoxy;Y is a bond or an alkylene chain of 1,2 or 3 carbon atoms in length;R'is hydrogen; a carbocyclic or heterocyclic group having from 3 to 12 ring members; or a C1-8 hydrocarbyl group optionally substituted by one or more substituents selected from halogen (e. g. fluorine), hydroxy, C1-4 hydrocarbyloxy, amino, mono-ordi-Cl 4 hydrocarbylamino, and carbocyclic or heterocyclic groups having from 3 to 12 ring members, and wherein 1 or 2 of the carbon atoms of the hydrocarbyl group may optionally be replaced by an atom or group selected fromO, S, NH, SO, SO2 ;R2 is hydrogen; halogen;C14 alkoxy (e. g. methoxy); or aC14 hydrocarbyl group optionally substituted by halogen (e. g. fluorine), hydroxyl orC14 alkoxy (e. g. methoxy);R3 is selected from hydrogen and carbocyclic and heterocyclic groups having from 3 to 12 ring members; andR4 is hydrogen or a C1-4 hydrocarbyl group optionally substituted by halogen (e. g. fluorine), hydroxyl or C1-4 alkoxy (e. g. methoxy).

Inhibition by amine derivatives

Patent Number: US6989385 Applicant: Vertex Pharmaceuticals Incorporated Title: Pyrazole compounds useful as protein kinase inhibitors

Basic Structure:

Pyrazol1.jpeg

Derivatives of pyrimidine-pyrazole amine disclosed in US6989385 patent

Patent Number: US7008948 Applicant: Vertex Pharmaceuticals Incorporated Title: Fused pyrimidyl pyrazole compounds useful as protein kinase inhibitors

Basic Structure

Pyrazol2.jpeg

Derivatives of pyrimidine-pyrazole amine disclosed in US7008948 patent

Patent Number: US6977262 Assignee: Mitsubishi Pharma Corporation Title: Dihydropyrazolopyridine compounds and pharmaceutical use thereof

Basic Structure:

Pyrazol3.jpeg

Derivatives of pyrimidine-pyrazole amine disclosed in US6977262 patent

Patent Number: US6664247 Assignee: Vertex Pharmaceuticals Incorporated Title: Pyrazole compounds useful as protein kinase inhibitors

Basic Structure:

Pyrazol4.jpeg

Derivatives of pyrimidine-pyrazole amine disclosed in US6664247 patent

Patent Number: US2004224944 Assignee: VERTEX PHARMACEUTICALS INC Title: Pyrazole compounds useful as protein kinase inhibitors

Basic Structure:

Pyrazol5.jpeg

Derivatives of pyrimidine-pyrazole amine disclosed in US2004224944 patent

Other derivates for alopecia

GSK-3 Inhibition Mechanism - Phosphorylation

  • GSK-3 inhibition targets treatment of chemotherapy-induced alopecia source
  • In the canonical Wnt signaling cascade, adenomatous polyposis coli (APC), axin, and GSK3 constitute the so-called destruction complex, which controls the stability of beta-catenin. It is generally believed that four conserved Ser/Thr residues in the N terminus of beta-catenin are the pivotal targets for the constitutively active serine kinase GSK3. GSK3 covalently modifies beta-catenin by attaching phosphate groups (from ATP) to serine, and threonine residues. In so doing, the functional properties of the protein kinase’s substrate (beta-catenin) are modified.
  • In the absence of Wnt signals, glycogen synthase kinase (GSK) is presumed to phosphorylate the N-terminal end of beta-catenin, thus promote degradation of beta-catenin and subsequent ubiquitination and proteasomal targeting.
  • Exposure of cells to Wnts leads to inactivation of GSK-3 through an as yet unclear mechanism.The phosphoprotein Dishevelled is required, after receptor-ligand interaction, to transduce the signal that results in the inactivation of GSK-3. As a result, beta-catenin is dephosphorylated and escapes the ubiqduitylation-dependent destruction machinery.
  • Unphosphorylated beta-catanin accumulates in the cytoplasm and translocates to the nucleus, where it can associate with the TCF/LEFs and become a transcriptional transactivator.

More details on GSK-3

Key points

  • Beta-catenin phosphorylation at serine 45 (Ser45), threonine 41 (Thr41), Ser37, and Ser33 is critical for beta-catenin degradation. source
  • Regulation of beta-catenin phosphorylation is a central part of the canonical Wnt signaling pathway. source
  • Ser-X-X-X-Ser (X is any amino acid) motif is obligatory for beta-catenin phosphorylation by GSK3.source
  • Beta-catenin phosphorylation/degradation and its regulation by Wnt can occur normally in the absence of Thr41 as long as the Ser-X-X-X-Ser motif/spacing is preserved. [httSp://pubs.acs.org/cgi-bin/abstract.cgi/bichaw/2006/45/i16/abs/bi0601149.html source]

GK3 Inhibition:

  • GSK3 is regulated by phosphorylation.
  • Phosphorylation of GSK3beta on Ser9 (Ser21 in GSK3alpha) by protein kinase B (PKB) causes its inactivation is the primary mechanism responsible for growth factor inhibition of this kinase. Activation of GSK3beta is dependent upon the phosphorylation of Tyr216 (Tyr279 in GSK3alpha). Upon activation, it has been shown to phosphorylate a number of different cellular proteins, including p53, c-Myc, c-Jun, heat shock factor-1 (HSF-1), beta-catenin and cyclin D1. source
  • GSK3 is inhibited by phosphorylation of serine-9 or serine-21 in GSK3beta and GSK3alpha, respectively. source
  • GSK3’s substrate specificity is unique in that phosphorylation of substrate only occurs if a phosphoserine or phosphotyrosine is present four residues C-terminal to the site of GSK phosphorylation. source
  • A phosphorylation cascade starts from GSK3 itself and initiates it in beta-catenin. source
  • Thus our goal is to stop the phosphorylation of the serine and threonine residue of GSK3.
  • The figure below illustrates the phosphorylation mechanism of serine and threonine by ATP.
Phosphorylation mechanism source


  • We can't stop conversion of ADP to ATP that relaseas Phosphorous group causing Phosphorylation.
  • We can only block the oxygen atom on serine and threonine as a result which will in turn stop Phosphorylation.
  • The two probable ways of blocking the oxygen atom are (a) As oxygen is a Lewis acid with strong electron donating capacity, so usually a strong electron pair acceptor can easily bind to oxygen atom and preventing phosphorylation or (b) breaking of the -OH bond with the carbon atom.

Serine - pyrazole reaction

Serine and Pyrazole reaction source
  • The T-loop of GSK-3 is tyrosine phosphorylated at Y216 and Y279 in GSK-3b and GSK-3a, respectively, but not threonine phosphorylated. Y216/Y279 phosphorylation could play a role in forcing open the substrate (e.g, beta-catanin)-binding site.
  • Thus, T-loop tyrosine might facilitate substrate phosphorylation but is not strictly required for kinase activity.
  • Stimulation of cells with pyrazole compounds cause inactivation of GSK-3 through phosphorylation (S9 of GSK-3 beta and S21 of GSK-3 alpha), which inhibits GSK-3 activity. Thus leading to dephosphorylation of substrates (e.g., beta-catanin) resulting in their functional activation and consequent increased hair follicle morphogenisis.
  • Phosphorylation of S9/S21 creates a primed pesudosubstrate that binds intramolecularly to the positively charged pocket of the GSK-3. This folding precludes phosphorylation of substrates (eg., beta-catanin) because the catalytic groove is occupied. The mechanism of inhibition is competitive.
  • A consequence of this is that primed substrates, in high enough concentrations, out-compete the pesudosubstrate and thus become phosphorylated.
  • Thus, small molecule inhibitors modeled to fit in the positively charged pocket of the GSK-3 kinease domain could potentially be very effective for selective inhibition of primed substrates.

Proposed mechanisms to regulate GSK-3 source

  1. inactivation of GSK-3 through serine phosphorylation
  2. activation of GSK-3 through tyrosine phosphorylation
  3. inactivation of GSK-3 through tyrosine dephosphorylation
  4. Covalant modifications of substrates through priming phosphorylation
  5. inhibition or facilation of GSK-3 mediated substrate phosphorylation thriugh interation of GSK-3 with binding or scaffolding proteins
  6. targeting of GSK-3 to different subcellular localizations
  7. differential usage of isoforms or splice variants to alter subcellular localization or substrate specificity
  8. integration of parellel signals conveyed by a signal stimulus.

Key Finding

  • Pyrazole compounds with inhibition constant (Ki) of <0.1 mM are a good starting point for developing molecules that can inhibit serine/threonine protein kinase (such as GSK-3) and the proteins they help to regulate. source

Pathway associated with anti-androgen

  • Dihydrotestosterone
    • Formed by peripheral conversion of testosterone by 5-alpha reductase
    • Binds to androgen receptor on susceptible hair follicles
  • Hormone-receptor complex activates genes responsible for gradual transformation of large terminal follicles to miniaturized (progressive diminution of hair shaft diameter and length in response to systemic androgens) follicles
5-alpha-reductase inhibition.jpeg

Structure-Activity Relationships(SARs)

SAR map.gif

Pathway associated with Minoxidil (vasodilators)

Minoxidil is a well know drug used for the treatment of alopecia. A co-relation between Sesquiterpene lactone (Helenalin) produced from Arnica montana and Minoxidil is illustrated in the figure below. Arnica montana, a Vasodilator, acts on the NO/cGMP Pathway through T-cells, B-cells and epithelial cells & abrogates kappa B-driven gene expression.

Vasodiator-rev.jpg

Alopecia IPMap

Dolcera IPMap for Alopecia



Patent activity in China

Treatment approaches

Treatment approach Patent number Priority year Assignee/Inventor
Vasodilators CN1772105 2005 叶明伟
CN1772139 2005 王亚杰
CN1569080 2003 谈汝标
CN1506103 2002 赵章光
CN1403100 2001 范希田
CN1165181 1996 殷国健
CN1031022 1988 天津市轻工业化学研究所
Hair matrix activator CN1463693 2002 朱静建
Anti-androgen + Vasodilator CN1150043 1996 梅晓春

Details of treatment approaches

Patent number Patent title Treatment approach Composition nature Composition Composition action
CN1772105
YE MINGWEI (CN)
叶明伟 (2005) 		Chinese herbal medicine decoction for treating blood stasis obstruction type alopecia and its prepn
治疗瘀血阻滞型脱发的中草药汤剂及制备方法 		Vasodilators Herbal extract Astragalus root, prepared rhizome of rehmannia, white peony root, angelica, peach kernel and sufflower Promote blood circulation
CN1772139
WANG YAJIE (CN)
王亚杰 2005 		Alopecia areata treating medicine
一种治疗斑秃的药物 		Vasodilators Herbal extract Pinellia tuber, fleeceflower root, arborvitae seed, chickení s gizzard membrane, prepared rhizome of rehmannia, Poris cocos, Codonopsis pilosula, etc Promote blood circulation
CN1569080
TAN RUBIAO (CN)
谈汝标 2003 		Natural Chinese herb composition for treating alopecia and leucotrichia and its application
一种可用于治疗脱发、白发的天然中草药提取组合物及应用 		Vasodilators Herbal extract Ginger, Cinnamomum cassia, myrrh, clove, mace nutmeg, Loranthus mulberry mistletoe, rhizoma dioscoreae, ligustrum japonicum, drynaria, fleece-flower root, and black sesame seeds Enhances the hair growth and healthier hairs
CN1463693
朱静建 2002 		Hair growing preparation containing compound of Chinese medicine and Western medicine
一种含中西药复方的育发剂 		Hair matrix activator Mixture of Herbal extracts and western medicine Persimmon leaf, oriental arbor-vitae leaf, ginseng leaf, yellow qi, fruit of the glossy privet, polygonum multiflorum, Kudzu root, dry ginger; Plus：Minoxidil, Vitamins and derivative, cystine, serine, leucine. Better and faster hair growth
CN1506103
赵章光2002 		Hair follice activating liquid
毛囊激活液 		Vasodilators Herbal extract Ginseng, twists the stock blue, the licorice, the Sophora flavescens and hot peppers Activates the hair-follicle and enhances the hair growth.
CN1403100
范希田 2001 		Trichogen and its prepn
一种止脱生发药物及其制备方法 		Vasodilators Herbal extract Ginseng, ganoderma lucidum, Chinese rhubarb, polygonum multiflorum, Chinese prickly ash, ginger, grass seed Promote blood circulation and enhance hair growth
CN1165181
殷国健 1996 		Washing free shampoo for nourishing and growing hair
免洗养发生发香波 		Vasodilator Vitamin composition Vitamin P (Bioflavonoids), Vitamin B15, Vitamin B2, nicotinic acid, bromo—geramineum Stimulate hair growth
CN1150043
梅晓春 1996 		Efficient low-side effect external use medicine for curing seborrheic baldness
一种治疗脂溢性脱发的高效低副作用外用药物 		Anti-androgen + Vasodilator Mixture of Herbal extracts and organic compounds Polygonum multiflorum, Ligustrum lucidum, Morus alba, Rehmannia glutinosa, Eclipta prostrata, Saliva miltiorrhiza, Carthamus tinctorius, Cnidium monnieri, Sophora flavescens, Dictamnus dasycarpus, Kochia scoparia, and antioxidants Inhibit the excess secretion of the sebaceous glands, increase the blood circulation on scalp and enhance the hair growth
CN1031022
天津市轻工业化学研究所 1988 		Channel-stimulating and hair-growing hair shampoo
一种通络生发香波 		Vasodilators Herbal extract + detergent Herbal extracts, Penetration media, Detergents. Increases the blood circulation under the scalp, reduces the hair los


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Conclusions

  • Hair loss medication is a very active area of research and intellectual property development.
  • One of the most promising areas of development is the area of Anti-androgens.
  • The top companies are Merck, L’Oreal and Smithkline.

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