Banefoul
Member
something i was noticing so decided to look for more info.
check out the rats diets
"The C57BL/6 mice were housed on a lightdark cycle in a room with temperature (22 ±2°C) and humidity control. They were fed either a high-fat diet (HFD) (49% fat, 18% protein, 33% carbohydrate) or a standard mouse diet (STD) (8% fat, 19% protein, 73% carbohydrate). Six-week-old C57BL/6J male mice were given HFD or STD diets for 17 wks before drug treatment started. This diet treatment caused significantly higher body weight gain in high-fat fed male animals as compared to normal diet animals. Simultaneously, the animals in the high fat diet fed group showed significant loss of body hair, especially on the back. After this, mice were weighed and treated as per the following three groups, while the diet treatment continued."
what caused weight gain and loss of hair?
we then find out....
"These data indicate that compound 1 and compound 2 are able to stimulate hair growth in addition to decreasing body weight."
how was this done?
"Compound 1 and Compound 2 were administered orally in distilled water with 0.1 % Tween 80 one hour before the onset of the dark phase."
Hair growth stimulators
Jul 20, 2005 The present invention discloses method for modulating the growth of body and/or head/cranial hair on mammalian organisms, for example humans, by administering thereto, whether topically and/or systemically, therapeutically effective amounts of at least one cannabinoid ligands, in combination with or without other suitable therapeutically active agents. Skip to: Description · Claims · Patent History · Classifications
Description
FIELD OF INVENTION
The present invention discloses a process for modulating the growth of body and/or head/cranial hair on mammalian organisms, for example humans, by administering thereto, whether topically and/or systemically, therapeutically effective amounts of at least one cannabinoid modulators, in combination with or without other suitable therapeutically active agents.
BACKGROUND AND PRIOR ART
Cannabinoids are present in Indian hemp Cannabis saliva and have been well known for their medicinal properties for ages. Cannabinoids as a therapeutic agents is however a recent phenomenon. (Williamson E. M. & Evans E. J. Drugs 2000 December; 60(6): 1303-14) Research in this area over the last decade have provided very important information on the cannabinoid receptors and their agonists and antagonists.
There has been an increased interest among the different pharmaceutical companies in developing drugs for the treatment of diseases connected with disorders of the cannabinoid systems (Greenberg D. A, Drugs News & Perspectives 1999; 12: 458; Kulkarni S. K. & Ninan, Indian Journal of Pharmacology 2001; 33; 170-184; Piomelli D et. al., Trends Pharmacol Sci. 2000 June; 21(6); 218-24). Several compounds which are either CB1, CB2 &/or CB3 antagonists have been reported and are under various stages of development for e.g. SR-141716 A (Sanofi), CP-272871 (Pfizer), LY-320135 (Eli Lily), AM-630 (Alexis), SR-144528 (Sanofi) etc.
Compounds which mimic the actions of the cannabinoids are useful for preventing or reversing the symptoms that can be treated with cannabis, some of its derivatives, and synthetic cannabinoids in a human or other mammalian subject. Thus compounds which are modulators of cannabinoid receptors are known to be useful in the treatment or amelioration of disorders, in mammals, such as (a) pulmonary disorders including asthma, chronic bronchitis; (b) ocular disorders such as glaucoma; (c) allergies and allergic reactions; (d) inflammatory conditions like arthritis, inflammatory bowel disease; (e) pain, (f) immune system disorders like AIDS, lupus; (g) allograft rejections; (h) central nervous system disorders like Torette's syndrome, Parkinson's disease, Huntington's disease, epilepsy, various psychotic disorders like depression, manic depression etc.; (i) vomiting, nausea and vertigo; (O) obesity; (k) cognitive disorders such as Alzheimer's disease; (1) schizophrenia; (m) smoking cessation
Use of cyclooxygenase or a lipoxygenase inhibitor as hair growth modulators have been described in U.S. Pat. No. 6,465,421 & U.S. Pat. No. 5,928,654.
We herein disclose compounds, which are cannabinoid receptors ligands, as hair growth modulators suitable for use in mammals either alone or in combination with other suitable therapeutically active agents.
DESCRIPTION OF THE ACCOMPANYING DRAWINGS
FIGS. 1 and 2: Effect of Compound 2 on Hair Growth in C57BL/6J Mice
DETAILED DESCRIPTION
The present invention discloses compounds, which are cannabinoid receptors ligands, suitable for modulating hair growth in mammals. Several compounds which act as cannabinoid receptors ligands, their preparation and their use in medicine have been reported in U.S. 20050101592, U.S. 20050096379, U.S. Pat. No. 5,925,768, U.S. Pat. No. 6,344,474, U.S. Pat. No. 6,028,084, U.S. Pat. No. 5,462,960, EP 0656354, U.S. Pat. No. 6,432,984, U.S. Pat. No. 6,509,367, U.S. Pat. No. 5,624,941, U.S. 20010053788, U.S. Pat. No. 6,476,060, U.S. 2004039024, EP1230222, EP 122952, FR 2816938, FR 2761266, FR 2800375, EP 0656354, EP 0576357, WO 0170700, WO 02076949, WO 2005044822, WO 2004096801, WO 2004094429, WO 2004096794, WO 2004094421, WO 2004094417, WO 2004096763, WO 200435566, WO 2004048317, WO 2004037823, WO 2004017920, WO 2004029204, WO 2004026301, WO 2004021974, WO 03082833, WO 03027076, WO 03026648, WO 03026647, WO 03020217, WO 03082191, WO 03084930, WO 03084943, WO 0228346, WO 0158450, WO 0185092, WO 0132663, WO 0132629, WO 9719063. Other compounds having similar activity have been disclosed in J Pharmacology & Experimental Therapeutics, 2003, 306(1), 363-370; Bioorganic Medicinal Chemistry, 1997, 5, 1591-1600; J Med. Chem. 1999, 42, 769-776; Bioorg. Med. Chem. Lett., 1999, 9, 2233-2236; Bioorg. Med. Chem. 2003, 11, 251-263; Bioorg. Med. Chem. 2003, 11, 3121-3132; Bioorg. Med. Chem. 2004, 12, 393-404, J Biological Chemistry, 1996, 271, 6941-6946; J. Med. Chem., 2002, 45, 1748-1756; J. Med. Chem., 2002, 45, 2708-2719; J Med. Chem., 2002, 45, 3649-3659; J Med. Chem., 2002, 45, 1447-1459; J. Med. Chem., 2003, 46, 642-645; J. Med. Chem., 2004, 47, 627-643; J Pharmacology & Experimental Therapeutics, 2002, 301(3), 963-968; Molecular Pharmacology, 2002, 62(6), 1274-1287; Drugs Fut., 2002, 27 (Suppl. A): XVIIth Int. Symposium on Medicinal Chemistry, Chem. Pharm. Bull., 2002, 50, 1109-1113. However, use of such compounds as modulators of hair growth has not been envisaged.
In a specific embodiment, the present invention discloses use of compounds disclosed in any of the above references or pharmaceutical compositions containing them as modulators of hair growth in mammals either alone or in combination with one or more other suitable therapeutic agents.
A “cannabinoid receptor ligand” according to the present invention includes a cannabinoid receptor antagonist, agonist or an inverse agonist.
A “hair growth modulator” according to the present invention includes a compound which hair growth stimulant or a repressant.
In a further embodiment the present invention provides method of modulating hair growth in mammals by treatment with compounds which axe ligands of the cannabinoid receptors.
In one of its embodiments the suitable cannabinoid receptor ligands for use according to the present invention bind to CB1, CB2 and/or CB3 receptors.
In a preferred embodiment, the compounds may be selected from the group which are preferentially antagonist or an inverse agonists of the CB1 receptor.
Non-limiting examples of cannabinoid receptor ligands are Rimonabant or its analogues, SLV-319 and the like.
In a further embodiment, the present invention discloses compound of formula (I) or pharmaceutical composition containing the same, as modulators of hair growth in mammals,
wherein,
R1 represents substituted or unsubstituted groups selected from (C3-C7)cycloalkyl, (C3-C7)cycloalkenyl, bicycloalkyl, bicycloalkenyl, aryl, aralkyl, heterocyclyl, heteroaryl, heterocyclyl(C1-C12)alkyl & heteroar(C1-C12)alkyl;
R2 represents a substituted or unsubstituted single or used heteroaromatic or a heterocyclic group containing one or more heteroatoms selected from N, O or S;
R3 represents hydrogen, halo, cyano, nitro, (C1-C12) substituted or unsubstituted alkyl, (C1-C12) substituted or unsubstituted haloalkyl, hydroxyalkyl, cycloalkyl, alkylsulfonyl groups;
X is either a direct bond or a group —(CH2)nN(R4)—, wherein R4 is H, or a (C1-C3)alkyl and n is 0-2;
R represents —NR5R6 where R5 is either H or (C1-C6)alkyl; R6 is
where Ra is (C1-C6)alkyl or Ra forms a bridge with one of the atoms of the heterocyclic radical formed by —NRbRc;
Rb and Ro represents substituted or unsubstituted groups selected from alkyl, aralkyl or alkenyl or Rb & Rc together with the nitrogen atom to which they are bonded, form a 5 to 8 membered saturated or unsaturated heterocyclic radical which may be optionally substituted and may be fused.
In yet another embodiment, the present invention discloses compound of formula (Ia) or pharmaceutical composition containing the same, as regulators/promoters/stimulators of hair growth in mammals,
wherein,
‘R7’ and ‘R8’ are the same or different and represent phenyl, thienyl or pyridyl groups, which may be optionally substituted with 1-3 substituents Y, which may be same or different and selected from the group C1-3-alkyl or alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C1-2)-amino, mono- or dialkyl (C1-3)-alkyl sulfonyl, dimethylsulfamido, C1-3-alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl, or R7 and/or & represent naphtyl; ‘R9’ represents hydrogen, hydroxy, C1-3-alkoxy, acetyloxy or propionyloxy;
‘Aa’ represents one of the groups (i), (ii), (iii), (iv) or (v)
wherein
‘R11’ and ‘R12’ independently of each other represent hydrogen or C1-8 branched or unbranched alkyl or C3-8 cycloalkyl or ‘R11’ represents acetamido or dimethylamino or 2,2,2-trifluroethyl or phenyl or pyridyl with the proviso that R12 represents hydrogen
‘R13’ represents hydrogen or C1-3 unbranched alkyl;
‘Bb’ represents sulfonyl or carbonyl;
‘R10’ represents benzyl, phenyl, thienyl or pyridyl which may be substituted with 1,2 or 3 substitutents Y, which can be the same or different, or ‘R10’ represents C1-8 branched or unbranched alkyl or C3-6 cycloalkyl, or ‘R10’ represents naphthyl.
The present invention also envisages the use of compounds, which are potentially suitable as cannabinoid receptors ligands as modulators of hair growth in mammals.
The present invention also discloses use of cannabinoid receptors ligands, in combination with other suitable therapeutically active agents for e.g. an inhibitor of cyclooxygenase or 5-lipoxygenase, or other hair growth modulators as are known in the art, as modulators of hair growth in mammals. Preferably, the other therapeutically active agent may be selected from Dutasteride, Finasteride, Minoxidil, Fluorominoxidil, Fluridil, Viprostol, Trequinsin hydrochloride, Namindil and Procyanidin B-2.
The quantity of active component, according to the present invention, in the pharmaceutical composition and unit dosage form thereof may be varied or adjusted widely depending upon the particular application method, the potency of the particular compound and the desired concentration. Generally, the quantity of active component will range between 0.5% to 90% by weight of the composition.
The precise dose and method of administration of cannabinoid receptors ligands to be used according to the present invention, will be determined by a number of factors, which will be apparent to those skilled in the art, in light of the disclosure herein.
Any suitable cannabinoid receptors ligands may be employed. A cannabinoid receptors ligands will be suitable if:
(a) at the dose and method of administration to the mammalian subject, it is not acutely toxic, and does not result in chronic toxicity disproportionate to the therapeutic benefit derived from treatment; and
(b) at the dose and method of administration to the mammalian subject it modulates hair growth in the subject.
Methods for conducting toxicity studies are known in the art.
The patient is preferably mammalian. In one embodiment the patient in which hair growth is modulated is a human. In another embodiment, it is a domestic animal such as cat, dog or horse.
In one embodiment of the invention, there is provided a method of modulating hair growth in mammalian patient in need thereof. The method comprises: selecting a patient in need of modulating hair growth, and administering a suitable cannabinoid receptor ligand.
In an embodiment is provided a topical formulation comprising atleast one caunabinoid receptor ligand, as a hair growth stimulant. The topical formulation may optionally contain one or more further hair growth stimulant. The formulation may further comprise other pharmaceutically acceptable excipients, suitable for suitably formulating the composition. The formulation may be prepared by techniques known in the art.
In one embodiment of the invention, there is provided a kit containing a cannabinoid receptor ligand and a pharmaceutically acceptable excipient. In one embodiment, the kit further comprises of, instnrctions for administering the cannabinoid receptor ligand to modulate hair growth in a mammalian subject. In yet another embodiment the kit still further comprises a means to administer the cannabinoid receptor ligand. Such kits may be prepared by techniques known.
Representative compounds suitable for carrying out the present invention includes;
Compound Structure IUPAC name Compound 1 Hydrochloride salt of 5-(5-Chloro- thiophen-2-yl)-1-(2,4-dichloro- phenyl)-4-methyl-1H-pyrazole-3- caxboxylic acid piperidin-1-ylamide Compound 2 5-(4-Chloro-phenyl)-1-(2,4-dichloro- phenyl)-1H-pyrazole-3-carboxylic acid ethyl ester Compound 3 4-Chloro-N-{[3-(4-chloro-phenyl)-4- phenyl-4,5-dihydro-pyrazol-1-yl]- methylamino-methylene}-benzene sulfonamide Compound 4 4-Chloro-N-{[3-(4-chloro-phenyl)-4- phenyl-4,5-dihydro-pyrazol-1-yl]- methylamino-methylene}-benzene sulfonamide
The present invention is illustrated by the following examples, which are provided for the sake of illustrations only and should not be construed as limiting the scope of the invention in any way.
EXAMPLE
Effect of Compound 1 and Compound 2 on Hair Growth and Body Weight in Male C57BL/6 Mice
The C57BL/6 mice were housed on a lightdark cycle in a room with temperature (22±2° C.) and humidity control. They were fed either a high-fat diet (HFD) (49% fat, 18% protein, 33% carbohydrate) or a standard mouse diet (STD) (8% fat, 19% protein, 73% carbohydrate). Six-week-old C57BL/6J male mice were given HFD or STD diets for 17 wks before drug treatment started. This diet treatment caused significantly higher body weight gain in high-fat fed male animals as compared to normal diet animals. Simultaneously, the animals in the high fat diet fed group showed significant loss of body hair, especially on the back. After this, mice were weighed and treated as per the following three groups, while the diet treatment continued.
High-fat diet fed & vehicle treated (HFD-V),
High-fat diet fed & treated with 10 mg/kg Compound 2 (HFD-R 10 mg)
High-fat diet fed & treated with 10 mg/kg Compound 1 (HD-ZY 10 mg)
Compound 1 and Compound 2 were administered orally in distilled water with 0.1% Tween 80 one hour before the onset of the dark phase.
The animals were observed daily. Body weights were recorded daily, and the animals were photographed on 28th day on the back, The results are mentioned in Table 1 and Table 2. It indicates that the treatment with 10 mg/kg Compound 1, has significantly enhanced the growth of body hair. The same treatment has resulted decrease in body weight.
TABLE 1 Effect of different treatments on the hair growth on male C57BL/6J mice Table indicate the bald area (where hair growth or pigmentation has not appeared) after 28th day of dosing (n = 6) Group Area (cm2) (Mean ± Standard Error Mean) HFD-V 0.346 ± 0.079 HFD-Compound 2 0.156 ± 0.068 HFD- Compound 1 0.011 ± 0.223
TABLE 2 Effect of different treatments on the body weight in male C57BL/6J mice (n = 6) Group Body Weight on Day 0 (g) HFD-V 30.5 ± 1.3 HFD- Compound 2 30.5 ± 1.6 HFD- Compound 1 29.2 ± 1.1 Body Weight on Day 28 (g) HFD-V 29.7 ± 1.1 HFD- Compound 2 27.1 ± 1.1 HFD- Compound 1 26.9 ± 1.1 Change in Body Weight (g) in 28 days versus Day 0 HFD-V −0.8 ± 0.4 HFD- Compound 2 −3.5 ± 0.8 HFD- Compound 1 −1.7 ± 0.5 Change in Body Weight (g) versus HFD-V HFD-V HFD- Compound 2 −9.7 ± 2.8 HFD- Compound 1 −3.3 ± 1.8
These data indicate that compound 1 and compound 2 are able to stimulate hair growth in addition to decreasing body weight.
Claims
1-24. (canceled)
25. A method for modulating hair growth in a mammalian subject in need thereof comprising administering an effective amount of a cannabinoid receptor ligand to the mammalian subject.
26. The method according to claim 25, wherein the cannabinoid receptor ligand binds to a cannabinoid receptor subtype selected from the group consisting of CB1, CB2 and CB3 receptors.
27. The method according to claim 25, wherein the cannabinoid receptor ligand is selected from the group consisting of:
(a) a cannabinoid receptor ligand of formula
(b) a cannabinoid receptor ligand of formula,
wherein,
R1 represents a substituted or unsubstituted group selected from the group consisting of (C3-C7)cycloalkyl, (C3-C7)cycloalkenyl, bicycloalkyl, bicycloalkenyl, aryl, aralkyl, heterocyclyl, heteroaryl, heterocyclyl(C1-C12)alkyl and heteroaryl(C1-C12)alkyl;
R2 represents a substituted or unsubstituted single or fused heteroaromatic or a heterocyclic group containing one or more heteroatoms selected from N, O or S;
R3 represents a group selected from the group consisting hydrogen, halo, cyano, nitro, substituted or unsubstituted(C1-C12)alkyl, substituted or unsubstituted halo(C1-C12)alkyl, hydroxyalkyl, cycloalkyl, and alkylsulfonyl X is either a bond or a group —(CH2)nN(R4)—, wherein R4 is H, or (C1-C3)alkyl and n is 0-2;
R represents —NR5R6 where R5 is either H or (C1-C6) alkyl; R6 is
where Ra is (C1-C6)alkyl or Ra forms a bridge with one of the atoms of the heterocyclic radical formed by —NRbRc;
Rb and Rc are the same or different and represent a substituted or unsubstituted group selected from alkyl, aralkyl or alkenyl or Rb and Rc together with the nitrogen atom to which they are bonded, form a 5 to 8 membered saturated or unsaturated heterocyclic radical which may be optionally substituted and may be fused;
(c) a cannabinoid receptor ligand of formula
wherein,
R7 and R8 are the same or different and represent phenyl, thienyl or pyridyl, which may be optionally substituted with 1 to 3 substituents Y, which are the same or different and are selected from the group consisting of (C1-3)alkyl, or (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C1-2)-amino, mono- or dialkyl (C1-3)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R7 or R8 or both represent naphtyl; R9 represents a group selected from the group consisting of hydrogen, hydroxy, (C1-3)alkoxy, acetyloxy and propionyloxy;
Aa represents one of the groups (i), (ii), (iii), (iv) or (v)
wherein
R11 and R12 independently of each other represent hydrogen or branched or unbranched (C1-8)alkyl or cyclo (C3-8)alkyl; or if R11 represents acetamido, dimethylamino, 2,2,2-trifluroethyl, phenyl or pyridyl, R12 represents hydrogen;
R13 represents hydrogen or unbranched (C1-3)alkyl;
Bb represents sulfonyl or carbonyl;
R10 represents benzyl, phenyl, thienyl or pyridyl which may be substituted with 1, 2 or 3 substituents Y, which are the same or different, and are selected from the group consisting of
(C1-3)alkyl, (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C1-2)-amino, mono- or dialkyl (C, 3)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R10 represents branched or unbranched (C1-8)alkyl or cyclo (C3-6)alkyl, or R10 represents naphthyl.
28. The method according to claim 25 wherein the cannabinoid receptor ligand is of formula
29. The method according to claim 25 wherein the cannabinoid receptor ligand is of formula
30. A method for stimulating hair growth in a mammalian subject in need thereof comprising administering an effective amount of a cannabinoid receptor ligand to the mammalian subject.
31. The method according to claim 30, wherein the cannabinoid receptor ligand binds to a cannabinoid receptor subtype selected from the group consisting of CB1, CB2 and CB3 receptors.
32. The method according to claim 30, wherein the cannabinoid receptor ligand is selected from the group consisting of:
(a) a cannabinoid receptor ligand of formula
(b) a cannabinoid receptor ligand of formula,
wherein,
R1 represents a substituted or unsubstituted group selected from the group consisting of (C3-C7)cycloalkyl, (C3-C7)cycloalkenyl, bicycloalkyl, bicycloalkenyl, aryl, aralkyl, heterocyclyl, heteroaryl, heterocyclyl(C1-C12)alkyl and heteroaryl(C1-C12)alkyl;
R2 represents a substituted or unsubstituted single or fused heteroaromatic or a heterocyclic group containing one or more heteroatoms selected from N, O or S;
R3 represents a group selected from the group consisting hydrogen, halo, cyano, nitro, substituted or unsubstituted(C1-C12)alkyl, substituted or unsubstituted halo(C1-C12)alkyl, hydroxyalkyl, cycloalkyl, and alkylsulfonyl X is either a bond or a group —(CH2)nN(R4)—, wherein R4 is H, or (C1-C3)alkyl and n is 0-2;
R represents —NR5R6 where R5 is either H or (C1-C6) alkyl; R6 is
where Ra is (C1-C6)alkyl or Ra forms a bridge with one of the atoms of the heterocyclic radical formed by —NRbRc;
Rb and Rc are the same or different and represent a substituted or unsubstituted group selected from alkyl, aralkyl or alkenyl or Rb and Rc together with the nitrogen atom to which they are bonded, form a 5 to 8 membered saturated or unsaturated heterocyclic radical which may be optionally substituted and may be fused;
(c) a cannabinoid receptor ligand of formula
wherein,
R7 and R8 are the same or different and represent phenyl, thienyl or pyridyl, which may be optionally substituted with 1 to 3 substituents Y, which are the same or different and are selected from the group consisting of
(C1-3)alkyl, (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C, 2)-amino, mono- or dialkyl (C, 3)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R7 or R8 or both represent naphtyl; R9 represents a group selected from the group consisting of hydrogen, hydroxy, (C1-3)alkoxy, acetyloxy and propionyloxy;
Aa represents one of the groups (i), (ii), (iii), (iv) or (v)
wherein
R11 and R12 independently of each other represent hydrogen or branched or unbranched (C1-8)alkyl or cyclo (C3-8)alkyl; or if R11 represents acetamido, dimethylamino, 2,2,2-trifluroethyl, phenyl or pyridyl, R12 represents hydrogen;
R13 represents hydrogen or unbranched (C1-3)alkyl;
Bb represents sulfonyl or carbonyl;
R10 represents benzyl, phenyl, thienyl or pyridyl which may be substituted with 1, 2 or 3 substituents Y, which are the same or different, and are selected from the group consisting of
(C1-3)alkyl, (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C, 2)-amino, mono- or dialkyl (C, 3)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R10 represents branched or unbranched (C1-8)alkyl or cyclo (C3-6)alkyl, or R10 represents naphthyl.
33. The method according to claim 30 wherein the cannabinoid receptor ligand is of formula
34. The method according to claim 30 wherein the cannabinoid receptor ligand is of formula
35. A composition comprising a cannabinoid receptor ligand selected from the group consisting of:
(a) a cannabinoid receptor ligand of formula
(b) a cannabinoid receptor ligand of formula,
wherein, R1 represents a substituted or unsubstituted group selected from the group consisting of (C3-C7)cycloalkyl, (C3-C7)cycloalkenyl, bicycloalkyl, bicycloalkenyl, aryl, aralkyl, heterocyclyl, heteroaryl, heterocyclyl(C1-C12)alkyl and heteroaryl(C1-C12)alkyl; R2 represents a substituted or unsubstituted single or fused heteroaromatic or a heterocyclic group containing one or more heteroatoms selected from N, O or S; R3 represents a group selected from the group consisting hydrogen, halo, cyano, nitro, substituted or unsubstituted(C1-C12)alkyl, substituted or unsubstituted halo(C1-C12)alkyl, hydroxyalkyl, cycloalkyl, and alkylsulfonyl; X is either a bond or a group —(CH2)nN(R4)—, wherein R4 is H, or (C1-C3)alkyl and n is 0-2; R represents —NR5R6 where R5 is either H or (C1-C6) alkyl; R6 is where Ra is (C1-C6)alkyl or Ra forms a bridge with one of the atoms of the heterocyclic radical formed by —NRbRc; Rb and Rc are the same or different and represent a substituted or unsubstituted group selected from alkyl, aralkyl or alkenyl or Rb and Rc together with the nitrogen atom to which they are bonded, form a 5 to 8 membered saturated or unsaturated heterocyclic radical which may be optionally substituted and may be fused; (b) a cannabinoid receptor ligand of formula wherein, R7 and R8 are the same or different and represent phenyl, thienyl or pyridyl, which may be optionally substituted with 1 to 3 substituents Y, which are the same or different and are selected from the group consisting of (C1-3)alkyl, (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C1-2)-amino, mono- or dialkyl (C13)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R7 or R8 or both represent naphtyl; R9 represents a group selected from the group consisting of hydrogen, hydroxy, (C1-3)alkoxy, acetyloxy and propionyloxy; Aa represents one of the groups (i), (ii), (iii), (iv) or (v) wherein R11 and R12 independently of each other represent hydrogen or branched or unbranched (C1-8)alkyl or cyclo (C3-8)alkyl; or if R11 represents acetamido, dimethylamino, 2,2,2-trifluroethyl, phenyl or pyridyl, R12 represents hydrogen;
R13 represents hydrogen or unbranched (C1-3)alkyl; Bb represents sulfonyl or carbonyl; R10 represents benzyl, phenyl, thienyl or pyridyl which may be substituted with 1, 2 or 3 substituents Y, which are the same or different, and are selected from the group consisting of (C1-3)alkyl, (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C12)— amino, mono- or dialkyl (C13)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R10 represents branched or unbranched (C1-8)alkyl or cyclo (C3-6)alkyl, or R10 represents naphthyl; and a pharmeutically acceptable excipient.
36. The composition according to claim 35 wherein the cannabinoid receptor ligand is of formula
37. A composition according to claim 35 wherein the cannabinoid receptor ligand is of formula
38. A composition according to claim 35 further comprising another compound which is a hair growth modulator.
39. A composition according to claim 36 further comprising another compound which is a hair growth modulator.
40. A composition according to claim 37 further comprising another compound which is a hair growth modulator.
41. A composition according to claim 38, wherein the hair growth modulator is at least one of Dutasteride, Finasteride, Minoxidil, Fluorominoxidil, Fluridil, Viprostol, Trequinsin hydrochloride, Namindil and Procyanidin B-2.
42. A composition according to claim 39, wherein the hair growth modulator is at least one of Dutasteride, Finasteride, Minoxidil, Fluorominoxidil, Fluridil, Viprostol, Trequinsin hydrochloride, Namindil and Procyanidin B-2.
43. A composition according to claim 40, wherein the hair growth modulator is at least one of Dutasteride, Finasteride, Minoxidil, Fluorominoxidil, Fluridil, Viprostol, Trequinsin hydrochloride, Namindil and Procyanidin B-2.
44. A kit comprising a pharmaceutical composition comprising a cannabinoid receptor ligand and a pharmaceutically acceptable excipient.
45. A kit according to claim 44, further comprising instructions for administering a cannabinoid receptor ligand to modulate hair growth in a mammalian subject.
46. A kit according to claim 44, further comprising a means to administer the cannabinoid receptor ligand.
47. The kit according to claim 44 wherein the cannabinoid receptor ligand is selected from the group consisting of:
(a) a cannabinoid receptor ligand of formula
(b) a cannabinoid receptor ligand of formula,
wherein,
R1 represents a substituted or unsubstituted group selected from the group consisting of (C3-C7)cycloalkyl, (C3-C7)cycloalkenyl, bicycloalkyl, bicycloalkenyl, aryl, aralkyl, heterocyclyl, heteroaryl, heterocyclyl(C1-C12)alkyl and heteroaryl(C1-C12)alkyl;
R2 represents a substituted or unsubstituted single or fused heteroaromatic or a heterocyclic group containing one or more heteroatoms selected from N, O or S;
R3 represents a group selected from the group consisting hydrogen, halo, cyano, nitro, substituted or unsubstituted(C1-C12)alkyl, substituted or unsubstituted halo(C1-C12)alkyl, hydroxyalkyl, cycloalkyl, and alkylsulfonyl X is either a bond or a group —(CH2)nN(R4)—, wherein R4 is H, or (C1-C3)alkyl and n is 0-2;
R represents —NR5R6 where R5 is either H or (C1-C6) alkyl; R6 is
where Ra is (C1-C6)alkyl or Ra forms a bridge with one of the atoms of the heterocyclic radical formed by —NRbRc;
Rb and Rc are the same or different and represent a substituted or unsubstituted group selected from alkyl, aralkyl or alkenyl or Rb and Rc together with the nitrogen atom to which they are bonded, form a 5 to 8 membered saturated or unsaturated heterocyclic radical which may be optionally substituted and may be fused;
(d) a cannabinoid receptor ligand of formula
wherein,
R7 and R8 are the same or different and represent phenyl, thienyl or pyridyl, which may be optionally substituted with 1 to 3 substituents Y, which are the same or different and are selected from the group consisting of
(C1-3)alkyl, or (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C1-2)-amino, mono- or dialkyl (C1-3)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R7 or R8 or both represent naphtyl; R9 represents a group selected from the group consisting of hydrogen, hydroxy, (C1-3)alkoxy, acetyloxy and propionyloxy;
Aa represents one of the groups (i), (ii), (iii), (iv) or (v)
wherein
R11 and R12 independently of each other represent hydrogen or branched or unbranched (C1-8)alkyl or cyclo (C3-8)alkyl; or if R11 represents acetamido, dimethylamino, 2,2,2-trifluroethyl, phenyl or pyridyl, R12 represents hydrogen;
R13 represents hydrogen or unbranched (C1-3)alkyl;
Bb represents sulfonyl or carbonyl;
R10 represents benzyl, phenyl, thienyl or pyridyl which may be substituted with 1, 2 or 3 substituents Y, which are the same or different, and are selected from the group consisting of (C1-3)alkyl, (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C12)— amino, mono- or dialkyl (C13)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R10 represents branched or unbranched (C1-8)alkyl or cyclo (C3-6)alkyl, or R10 represents naphthyl.
48. The compound of the formula
Patent History
Application number: 20060025448
Type: Application
Filed: Jul 20, 2005
Issued: Feb 02, 2006
Assignee:
Inventors: Braj Lohray (Ahmedabad), Vidya Lohray (Ahmedabad), Mukul Jain (Ahmedabad), Brijesh Srivastava (Ahmedabad)
Application Serial: 11/185,919
Classifications
Current U.S. Class: 514/326.000; 514/406.000
International Classification: A61K 31/454 (20060101); A61K 31/4152 (20060101);
http://patents.justia.com/patent/20060025448
http://www.google.nl/patents/EP1623741A2?cl=en
check out the rats diets
"The C57BL/6 mice were housed on a lightdark cycle in a room with temperature (22 ±2°C) and humidity control. They were fed either a high-fat diet (HFD) (49% fat, 18% protein, 33% carbohydrate) or a standard mouse diet (STD) (8% fat, 19% protein, 73% carbohydrate). Six-week-old C57BL/6J male mice were given HFD or STD diets for 17 wks before drug treatment started. This diet treatment caused significantly higher body weight gain in high-fat fed male animals as compared to normal diet animals. Simultaneously, the animals in the high fat diet fed group showed significant loss of body hair, especially on the back. After this, mice were weighed and treated as per the following three groups, while the diet treatment continued."
what caused weight gain and loss of hair?
we then find out....
"These data indicate that compound 1 and compound 2 are able to stimulate hair growth in addition to decreasing body weight."
how was this done?
"Compound 1 and Compound 2 were administered orally in distilled water with 0.1 % Tween 80 one hour before the onset of the dark phase."
Hair growth stimulators
Jul 20, 2005 The present invention discloses method for modulating the growth of body and/or head/cranial hair on mammalian organisms, for example humans, by administering thereto, whether topically and/or systemically, therapeutically effective amounts of at least one cannabinoid ligands, in combination with or without other suitable therapeutically active agents. Skip to: Description · Claims · Patent History · Classifications
Description
FIELD OF INVENTION
The present invention discloses a process for modulating the growth of body and/or head/cranial hair on mammalian organisms, for example humans, by administering thereto, whether topically and/or systemically, therapeutically effective amounts of at least one cannabinoid modulators, in combination with or without other suitable therapeutically active agents.
BACKGROUND AND PRIOR ART
Cannabinoids are present in Indian hemp Cannabis saliva and have been well known for their medicinal properties for ages. Cannabinoids as a therapeutic agents is however a recent phenomenon. (Williamson E. M. & Evans E. J. Drugs 2000 December; 60(6): 1303-14) Research in this area over the last decade have provided very important information on the cannabinoid receptors and their agonists and antagonists.
There has been an increased interest among the different pharmaceutical companies in developing drugs for the treatment of diseases connected with disorders of the cannabinoid systems (Greenberg D. A, Drugs News & Perspectives 1999; 12: 458; Kulkarni S. K. & Ninan, Indian Journal of Pharmacology 2001; 33; 170-184; Piomelli D et. al., Trends Pharmacol Sci. 2000 June; 21(6); 218-24). Several compounds which are either CB1, CB2 &/or CB3 antagonists have been reported and are under various stages of development for e.g. SR-141716 A (Sanofi), CP-272871 (Pfizer), LY-320135 (Eli Lily), AM-630 (Alexis), SR-144528 (Sanofi) etc.
Compounds which mimic the actions of the cannabinoids are useful for preventing or reversing the symptoms that can be treated with cannabis, some of its derivatives, and synthetic cannabinoids in a human or other mammalian subject. Thus compounds which are modulators of cannabinoid receptors are known to be useful in the treatment or amelioration of disorders, in mammals, such as (a) pulmonary disorders including asthma, chronic bronchitis; (b) ocular disorders such as glaucoma; (c) allergies and allergic reactions; (d) inflammatory conditions like arthritis, inflammatory bowel disease; (e) pain, (f) immune system disorders like AIDS, lupus; (g) allograft rejections; (h) central nervous system disorders like Torette's syndrome, Parkinson's disease, Huntington's disease, epilepsy, various psychotic disorders like depression, manic depression etc.; (i) vomiting, nausea and vertigo; (O) obesity; (k) cognitive disorders such as Alzheimer's disease; (1) schizophrenia; (m) smoking cessation
Use of cyclooxygenase or a lipoxygenase inhibitor as hair growth modulators have been described in U.S. Pat. No. 6,465,421 & U.S. Pat. No. 5,928,654.
We herein disclose compounds, which are cannabinoid receptors ligands, as hair growth modulators suitable for use in mammals either alone or in combination with other suitable therapeutically active agents.
DESCRIPTION OF THE ACCOMPANYING DRAWINGS
FIGS. 1 and 2: Effect of Compound 2 on Hair Growth in C57BL/6J Mice
DETAILED DESCRIPTION
The present invention discloses compounds, which are cannabinoid receptors ligands, suitable for modulating hair growth in mammals. Several compounds which act as cannabinoid receptors ligands, their preparation and their use in medicine have been reported in U.S. 20050101592, U.S. 20050096379, U.S. Pat. No. 5,925,768, U.S. Pat. No. 6,344,474, U.S. Pat. No. 6,028,084, U.S. Pat. No. 5,462,960, EP 0656354, U.S. Pat. No. 6,432,984, U.S. Pat. No. 6,509,367, U.S. Pat. No. 5,624,941, U.S. 20010053788, U.S. Pat. No. 6,476,060, U.S. 2004039024, EP1230222, EP 122952, FR 2816938, FR 2761266, FR 2800375, EP 0656354, EP 0576357, WO 0170700, WO 02076949, WO 2005044822, WO 2004096801, WO 2004094429, WO 2004096794, WO 2004094421, WO 2004094417, WO 2004096763, WO 200435566, WO 2004048317, WO 2004037823, WO 2004017920, WO 2004029204, WO 2004026301, WO 2004021974, WO 03082833, WO 03027076, WO 03026648, WO 03026647, WO 03020217, WO 03082191, WO 03084930, WO 03084943, WO 0228346, WO 0158450, WO 0185092, WO 0132663, WO 0132629, WO 9719063. Other compounds having similar activity have been disclosed in J Pharmacology & Experimental Therapeutics, 2003, 306(1), 363-370; Bioorganic Medicinal Chemistry, 1997, 5, 1591-1600; J Med. Chem. 1999, 42, 769-776; Bioorg. Med. Chem. Lett., 1999, 9, 2233-2236; Bioorg. Med. Chem. 2003, 11, 251-263; Bioorg. Med. Chem. 2003, 11, 3121-3132; Bioorg. Med. Chem. 2004, 12, 393-404, J Biological Chemistry, 1996, 271, 6941-6946; J. Med. Chem., 2002, 45, 1748-1756; J. Med. Chem., 2002, 45, 2708-2719; J Med. Chem., 2002, 45, 3649-3659; J Med. Chem., 2002, 45, 1447-1459; J. Med. Chem., 2003, 46, 642-645; J. Med. Chem., 2004, 47, 627-643; J Pharmacology & Experimental Therapeutics, 2002, 301(3), 963-968; Molecular Pharmacology, 2002, 62(6), 1274-1287; Drugs Fut., 2002, 27 (Suppl. A): XVIIth Int. Symposium on Medicinal Chemistry, Chem. Pharm. Bull., 2002, 50, 1109-1113. However, use of such compounds as modulators of hair growth has not been envisaged.
In a specific embodiment, the present invention discloses use of compounds disclosed in any of the above references or pharmaceutical compositions containing them as modulators of hair growth in mammals either alone or in combination with one or more other suitable therapeutic agents.
A “cannabinoid receptor ligand” according to the present invention includes a cannabinoid receptor antagonist, agonist or an inverse agonist.
A “hair growth modulator” according to the present invention includes a compound which hair growth stimulant or a repressant.
In a further embodiment the present invention provides method of modulating hair growth in mammals by treatment with compounds which axe ligands of the cannabinoid receptors.
In one of its embodiments the suitable cannabinoid receptor ligands for use according to the present invention bind to CB1, CB2 and/or CB3 receptors.
In a preferred embodiment, the compounds may be selected from the group which are preferentially antagonist or an inverse agonists of the CB1 receptor.
Non-limiting examples of cannabinoid receptor ligands are Rimonabant or its analogues, SLV-319 and the like.
In a further embodiment, the present invention discloses compound of formula (I) or pharmaceutical composition containing the same, as modulators of hair growth in mammals,
wherein,
R1 represents substituted or unsubstituted groups selected from (C3-C7)cycloalkyl, (C3-C7)cycloalkenyl, bicycloalkyl, bicycloalkenyl, aryl, aralkyl, heterocyclyl, heteroaryl, heterocyclyl(C1-C12)alkyl & heteroar(C1-C12)alkyl;
R2 represents a substituted or unsubstituted single or used heteroaromatic or a heterocyclic group containing one or more heteroatoms selected from N, O or S;
R3 represents hydrogen, halo, cyano, nitro, (C1-C12) substituted or unsubstituted alkyl, (C1-C12) substituted or unsubstituted haloalkyl, hydroxyalkyl, cycloalkyl, alkylsulfonyl groups;
X is either a direct bond or a group —(CH2)nN(R4)—, wherein R4 is H, or a (C1-C3)alkyl and n is 0-2;
R represents —NR5R6 where R5 is either H or (C1-C6)alkyl; R6 is
where Ra is (C1-C6)alkyl or Ra forms a bridge with one of the atoms of the heterocyclic radical formed by —NRbRc;
Rb and Ro represents substituted or unsubstituted groups selected from alkyl, aralkyl or alkenyl or Rb & Rc together with the nitrogen atom to which they are bonded, form a 5 to 8 membered saturated or unsaturated heterocyclic radical which may be optionally substituted and may be fused.
In yet another embodiment, the present invention discloses compound of formula (Ia) or pharmaceutical composition containing the same, as regulators/promoters/stimulators of hair growth in mammals,
wherein,
‘R7’ and ‘R8’ are the same or different and represent phenyl, thienyl or pyridyl groups, which may be optionally substituted with 1-3 substituents Y, which may be same or different and selected from the group C1-3-alkyl or alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C1-2)-amino, mono- or dialkyl (C1-3)-alkyl sulfonyl, dimethylsulfamido, C1-3-alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl, or R7 and/or & represent naphtyl; ‘R9’ represents hydrogen, hydroxy, C1-3-alkoxy, acetyloxy or propionyloxy;
‘Aa’ represents one of the groups (i), (ii), (iii), (iv) or (v)
wherein
‘R11’ and ‘R12’ independently of each other represent hydrogen or C1-8 branched or unbranched alkyl or C3-8 cycloalkyl or ‘R11’ represents acetamido or dimethylamino or 2,2,2-trifluroethyl or phenyl or pyridyl with the proviso that R12 represents hydrogen
‘R13’ represents hydrogen or C1-3 unbranched alkyl;
‘Bb’ represents sulfonyl or carbonyl;
‘R10’ represents benzyl, phenyl, thienyl or pyridyl which may be substituted with 1,2 or 3 substitutents Y, which can be the same or different, or ‘R10’ represents C1-8 branched or unbranched alkyl or C3-6 cycloalkyl, or ‘R10’ represents naphthyl.
The present invention also envisages the use of compounds, which are potentially suitable as cannabinoid receptors ligands as modulators of hair growth in mammals.
The present invention also discloses use of cannabinoid receptors ligands, in combination with other suitable therapeutically active agents for e.g. an inhibitor of cyclooxygenase or 5-lipoxygenase, or other hair growth modulators as are known in the art, as modulators of hair growth in mammals. Preferably, the other therapeutically active agent may be selected from Dutasteride, Finasteride, Minoxidil, Fluorominoxidil, Fluridil, Viprostol, Trequinsin hydrochloride, Namindil and Procyanidin B-2.
The quantity of active component, according to the present invention, in the pharmaceutical composition and unit dosage form thereof may be varied or adjusted widely depending upon the particular application method, the potency of the particular compound and the desired concentration. Generally, the quantity of active component will range between 0.5% to 90% by weight of the composition.
The precise dose and method of administration of cannabinoid receptors ligands to be used according to the present invention, will be determined by a number of factors, which will be apparent to those skilled in the art, in light of the disclosure herein.
Any suitable cannabinoid receptors ligands may be employed. A cannabinoid receptors ligands will be suitable if:
(a) at the dose and method of administration to the mammalian subject, it is not acutely toxic, and does not result in chronic toxicity disproportionate to the therapeutic benefit derived from treatment; and
(b) at the dose and method of administration to the mammalian subject it modulates hair growth in the subject.
Methods for conducting toxicity studies are known in the art.
The patient is preferably mammalian. In one embodiment the patient in which hair growth is modulated is a human. In another embodiment, it is a domestic animal such as cat, dog or horse.
In one embodiment of the invention, there is provided a method of modulating hair growth in mammalian patient in need thereof. The method comprises: selecting a patient in need of modulating hair growth, and administering a suitable cannabinoid receptor ligand.
In an embodiment is provided a topical formulation comprising atleast one caunabinoid receptor ligand, as a hair growth stimulant. The topical formulation may optionally contain one or more further hair growth stimulant. The formulation may further comprise other pharmaceutically acceptable excipients, suitable for suitably formulating the composition. The formulation may be prepared by techniques known in the art.
In one embodiment of the invention, there is provided a kit containing a cannabinoid receptor ligand and a pharmaceutically acceptable excipient. In one embodiment, the kit further comprises of, instnrctions for administering the cannabinoid receptor ligand to modulate hair growth in a mammalian subject. In yet another embodiment the kit still further comprises a means to administer the cannabinoid receptor ligand. Such kits may be prepared by techniques known.
Representative compounds suitable for carrying out the present invention includes;
Compound Structure IUPAC name Compound 1 Hydrochloride salt of 5-(5-Chloro- thiophen-2-yl)-1-(2,4-dichloro- phenyl)-4-methyl-1H-pyrazole-3- caxboxylic acid piperidin-1-ylamide Compound 2 5-(4-Chloro-phenyl)-1-(2,4-dichloro- phenyl)-1H-pyrazole-3-carboxylic acid ethyl ester Compound 3 4-Chloro-N-{[3-(4-chloro-phenyl)-4- phenyl-4,5-dihydro-pyrazol-1-yl]- methylamino-methylene}-benzene sulfonamide Compound 4 4-Chloro-N-{[3-(4-chloro-phenyl)-4- phenyl-4,5-dihydro-pyrazol-1-yl]- methylamino-methylene}-benzene sulfonamide
The present invention is illustrated by the following examples, which are provided for the sake of illustrations only and should not be construed as limiting the scope of the invention in any way.
EXAMPLE
Effect of Compound 1 and Compound 2 on Hair Growth and Body Weight in Male C57BL/6 Mice
The C57BL/6 mice were housed on a lightdark cycle in a room with temperature (22±2° C.) and humidity control. They were fed either a high-fat diet (HFD) (49% fat, 18% protein, 33% carbohydrate) or a standard mouse diet (STD) (8% fat, 19% protein, 73% carbohydrate). Six-week-old C57BL/6J male mice were given HFD or STD diets for 17 wks before drug treatment started. This diet treatment caused significantly higher body weight gain in high-fat fed male animals as compared to normal diet animals. Simultaneously, the animals in the high fat diet fed group showed significant loss of body hair, especially on the back. After this, mice were weighed and treated as per the following three groups, while the diet treatment continued.
High-fat diet fed & vehicle treated (HFD-V),
High-fat diet fed & treated with 10 mg/kg Compound 2 (HFD-R 10 mg)
High-fat diet fed & treated with 10 mg/kg Compound 1 (HD-ZY 10 mg)
Compound 1 and Compound 2 were administered orally in distilled water with 0.1% Tween 80 one hour before the onset of the dark phase.
The animals were observed daily. Body weights were recorded daily, and the animals were photographed on 28th day on the back, The results are mentioned in Table 1 and Table 2. It indicates that the treatment with 10 mg/kg Compound 1, has significantly enhanced the growth of body hair. The same treatment has resulted decrease in body weight.
TABLE 1 Effect of different treatments on the hair growth on male C57BL/6J mice Table indicate the bald area (where hair growth or pigmentation has not appeared) after 28th day of dosing (n = 6) Group Area (cm2) (Mean ± Standard Error Mean) HFD-V 0.346 ± 0.079 HFD-Compound 2 0.156 ± 0.068 HFD- Compound 1 0.011 ± 0.223
TABLE 2 Effect of different treatments on the body weight in male C57BL/6J mice (n = 6) Group Body Weight on Day 0 (g) HFD-V 30.5 ± 1.3 HFD- Compound 2 30.5 ± 1.6 HFD- Compound 1 29.2 ± 1.1 Body Weight on Day 28 (g) HFD-V 29.7 ± 1.1 HFD- Compound 2 27.1 ± 1.1 HFD- Compound 1 26.9 ± 1.1 Change in Body Weight (g) in 28 days versus Day 0 HFD-V −0.8 ± 0.4 HFD- Compound 2 −3.5 ± 0.8 HFD- Compound 1 −1.7 ± 0.5 Change in Body Weight (g) versus HFD-V HFD-V HFD- Compound 2 −9.7 ± 2.8 HFD- Compound 1 −3.3 ± 1.8
These data indicate that compound 1 and compound 2 are able to stimulate hair growth in addition to decreasing body weight.
Claims
1-24. (canceled)
25. A method for modulating hair growth in a mammalian subject in need thereof comprising administering an effective amount of a cannabinoid receptor ligand to the mammalian subject.
26. The method according to claim 25, wherein the cannabinoid receptor ligand binds to a cannabinoid receptor subtype selected from the group consisting of CB1, CB2 and CB3 receptors.
27. The method according to claim 25, wherein the cannabinoid receptor ligand is selected from the group consisting of:
(a) a cannabinoid receptor ligand of formula
(b) a cannabinoid receptor ligand of formula,
wherein,
R1 represents a substituted or unsubstituted group selected from the group consisting of (C3-C7)cycloalkyl, (C3-C7)cycloalkenyl, bicycloalkyl, bicycloalkenyl, aryl, aralkyl, heterocyclyl, heteroaryl, heterocyclyl(C1-C12)alkyl and heteroaryl(C1-C12)alkyl;
R2 represents a substituted or unsubstituted single or fused heteroaromatic or a heterocyclic group containing one or more heteroatoms selected from N, O or S;
R3 represents a group selected from the group consisting hydrogen, halo, cyano, nitro, substituted or unsubstituted(C1-C12)alkyl, substituted or unsubstituted halo(C1-C12)alkyl, hydroxyalkyl, cycloalkyl, and alkylsulfonyl X is either a bond or a group —(CH2)nN(R4)—, wherein R4 is H, or (C1-C3)alkyl and n is 0-2;
R represents —NR5R6 where R5 is either H or (C1-C6) alkyl; R6 is
where Ra is (C1-C6)alkyl or Ra forms a bridge with one of the atoms of the heterocyclic radical formed by —NRbRc;
Rb and Rc are the same or different and represent a substituted or unsubstituted group selected from alkyl, aralkyl or alkenyl or Rb and Rc together with the nitrogen atom to which they are bonded, form a 5 to 8 membered saturated or unsaturated heterocyclic radical which may be optionally substituted and may be fused;
(c) a cannabinoid receptor ligand of formula
wherein,
R7 and R8 are the same or different and represent phenyl, thienyl or pyridyl, which may be optionally substituted with 1 to 3 substituents Y, which are the same or different and are selected from the group consisting of (C1-3)alkyl, or (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C1-2)-amino, mono- or dialkyl (C1-3)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R7 or R8 or both represent naphtyl; R9 represents a group selected from the group consisting of hydrogen, hydroxy, (C1-3)alkoxy, acetyloxy and propionyloxy;
Aa represents one of the groups (i), (ii), (iii), (iv) or (v)
wherein
R11 and R12 independently of each other represent hydrogen or branched or unbranched (C1-8)alkyl or cyclo (C3-8)alkyl; or if R11 represents acetamido, dimethylamino, 2,2,2-trifluroethyl, phenyl or pyridyl, R12 represents hydrogen;
R13 represents hydrogen or unbranched (C1-3)alkyl;
Bb represents sulfonyl or carbonyl;
R10 represents benzyl, phenyl, thienyl or pyridyl which may be substituted with 1, 2 or 3 substituents Y, which are the same or different, and are selected from the group consisting of
(C1-3)alkyl, (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C1-2)-amino, mono- or dialkyl (C, 3)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R10 represents branched or unbranched (C1-8)alkyl or cyclo (C3-6)alkyl, or R10 represents naphthyl.
28. The method according to claim 25 wherein the cannabinoid receptor ligand is of formula
29. The method according to claim 25 wherein the cannabinoid receptor ligand is of formula
30. A method for stimulating hair growth in a mammalian subject in need thereof comprising administering an effective amount of a cannabinoid receptor ligand to the mammalian subject.
31. The method according to claim 30, wherein the cannabinoid receptor ligand binds to a cannabinoid receptor subtype selected from the group consisting of CB1, CB2 and CB3 receptors.
32. The method according to claim 30, wherein the cannabinoid receptor ligand is selected from the group consisting of:
(a) a cannabinoid receptor ligand of formula
(b) a cannabinoid receptor ligand of formula,
wherein,
R1 represents a substituted or unsubstituted group selected from the group consisting of (C3-C7)cycloalkyl, (C3-C7)cycloalkenyl, bicycloalkyl, bicycloalkenyl, aryl, aralkyl, heterocyclyl, heteroaryl, heterocyclyl(C1-C12)alkyl and heteroaryl(C1-C12)alkyl;
R2 represents a substituted or unsubstituted single or fused heteroaromatic or a heterocyclic group containing one or more heteroatoms selected from N, O or S;
R3 represents a group selected from the group consisting hydrogen, halo, cyano, nitro, substituted or unsubstituted(C1-C12)alkyl, substituted or unsubstituted halo(C1-C12)alkyl, hydroxyalkyl, cycloalkyl, and alkylsulfonyl X is either a bond or a group —(CH2)nN(R4)—, wherein R4 is H, or (C1-C3)alkyl and n is 0-2;
R represents —NR5R6 where R5 is either H or (C1-C6) alkyl; R6 is
where Ra is (C1-C6)alkyl or Ra forms a bridge with one of the atoms of the heterocyclic radical formed by —NRbRc;
Rb and Rc are the same or different and represent a substituted or unsubstituted group selected from alkyl, aralkyl or alkenyl or Rb and Rc together with the nitrogen atom to which they are bonded, form a 5 to 8 membered saturated or unsaturated heterocyclic radical which may be optionally substituted and may be fused;
(c) a cannabinoid receptor ligand of formula
wherein,
R7 and R8 are the same or different and represent phenyl, thienyl or pyridyl, which may be optionally substituted with 1 to 3 substituents Y, which are the same or different and are selected from the group consisting of
(C1-3)alkyl, (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C, 2)-amino, mono- or dialkyl (C, 3)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R7 or R8 or both represent naphtyl; R9 represents a group selected from the group consisting of hydrogen, hydroxy, (C1-3)alkoxy, acetyloxy and propionyloxy;
Aa represents one of the groups (i), (ii), (iii), (iv) or (v)
wherein
R11 and R12 independently of each other represent hydrogen or branched or unbranched (C1-8)alkyl or cyclo (C3-8)alkyl; or if R11 represents acetamido, dimethylamino, 2,2,2-trifluroethyl, phenyl or pyridyl, R12 represents hydrogen;
R13 represents hydrogen or unbranched (C1-3)alkyl;
Bb represents sulfonyl or carbonyl;
R10 represents benzyl, phenyl, thienyl or pyridyl which may be substituted with 1, 2 or 3 substituents Y, which are the same or different, and are selected from the group consisting of
(C1-3)alkyl, (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C, 2)-amino, mono- or dialkyl (C, 3)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R10 represents branched or unbranched (C1-8)alkyl or cyclo (C3-6)alkyl, or R10 represents naphthyl.
33. The method according to claim 30 wherein the cannabinoid receptor ligand is of formula
34. The method according to claim 30 wherein the cannabinoid receptor ligand is of formula
35. A composition comprising a cannabinoid receptor ligand selected from the group consisting of:
(a) a cannabinoid receptor ligand of formula
(b) a cannabinoid receptor ligand of formula,
wherein, R1 represents a substituted or unsubstituted group selected from the group consisting of (C3-C7)cycloalkyl, (C3-C7)cycloalkenyl, bicycloalkyl, bicycloalkenyl, aryl, aralkyl, heterocyclyl, heteroaryl, heterocyclyl(C1-C12)alkyl and heteroaryl(C1-C12)alkyl; R2 represents a substituted or unsubstituted single or fused heteroaromatic or a heterocyclic group containing one or more heteroatoms selected from N, O or S; R3 represents a group selected from the group consisting hydrogen, halo, cyano, nitro, substituted or unsubstituted(C1-C12)alkyl, substituted or unsubstituted halo(C1-C12)alkyl, hydroxyalkyl, cycloalkyl, and alkylsulfonyl; X is either a bond or a group —(CH2)nN(R4)—, wherein R4 is H, or (C1-C3)alkyl and n is 0-2; R represents —NR5R6 where R5 is either H or (C1-C6) alkyl; R6 is where Ra is (C1-C6)alkyl or Ra forms a bridge with one of the atoms of the heterocyclic radical formed by —NRbRc; Rb and Rc are the same or different and represent a substituted or unsubstituted group selected from alkyl, aralkyl or alkenyl or Rb and Rc together with the nitrogen atom to which they are bonded, form a 5 to 8 membered saturated or unsaturated heterocyclic radical which may be optionally substituted and may be fused; (b) a cannabinoid receptor ligand of formula wherein, R7 and R8 are the same or different and represent phenyl, thienyl or pyridyl, which may be optionally substituted with 1 to 3 substituents Y, which are the same or different and are selected from the group consisting of (C1-3)alkyl, (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C1-2)-amino, mono- or dialkyl (C13)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R7 or R8 or both represent naphtyl; R9 represents a group selected from the group consisting of hydrogen, hydroxy, (C1-3)alkoxy, acetyloxy and propionyloxy; Aa represents one of the groups (i), (ii), (iii), (iv) or (v) wherein R11 and R12 independently of each other represent hydrogen or branched or unbranched (C1-8)alkyl or cyclo (C3-8)alkyl; or if R11 represents acetamido, dimethylamino, 2,2,2-trifluroethyl, phenyl or pyridyl, R12 represents hydrogen;
R13 represents hydrogen or unbranched (C1-3)alkyl; Bb represents sulfonyl or carbonyl; R10 represents benzyl, phenyl, thienyl or pyridyl which may be substituted with 1, 2 or 3 substituents Y, which are the same or different, and are selected from the group consisting of (C1-3)alkyl, (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C12)— amino, mono- or dialkyl (C13)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R10 represents branched or unbranched (C1-8)alkyl or cyclo (C3-6)alkyl, or R10 represents naphthyl; and a pharmeutically acceptable excipient.
36. The composition according to claim 35 wherein the cannabinoid receptor ligand is of formula
37. A composition according to claim 35 wherein the cannabinoid receptor ligand is of formula
38. A composition according to claim 35 further comprising another compound which is a hair growth modulator.
39. A composition according to claim 36 further comprising another compound which is a hair growth modulator.
40. A composition according to claim 37 further comprising another compound which is a hair growth modulator.
41. A composition according to claim 38, wherein the hair growth modulator is at least one of Dutasteride, Finasteride, Minoxidil, Fluorominoxidil, Fluridil, Viprostol, Trequinsin hydrochloride, Namindil and Procyanidin B-2.
42. A composition according to claim 39, wherein the hair growth modulator is at least one of Dutasteride, Finasteride, Minoxidil, Fluorominoxidil, Fluridil, Viprostol, Trequinsin hydrochloride, Namindil and Procyanidin B-2.
43. A composition according to claim 40, wherein the hair growth modulator is at least one of Dutasteride, Finasteride, Minoxidil, Fluorominoxidil, Fluridil, Viprostol, Trequinsin hydrochloride, Namindil and Procyanidin B-2.
44. A kit comprising a pharmaceutical composition comprising a cannabinoid receptor ligand and a pharmaceutically acceptable excipient.
45. A kit according to claim 44, further comprising instructions for administering a cannabinoid receptor ligand to modulate hair growth in a mammalian subject.
46. A kit according to claim 44, further comprising a means to administer the cannabinoid receptor ligand.
47. The kit according to claim 44 wherein the cannabinoid receptor ligand is selected from the group consisting of:
(a) a cannabinoid receptor ligand of formula
(b) a cannabinoid receptor ligand of formula,
wherein,
R1 represents a substituted or unsubstituted group selected from the group consisting of (C3-C7)cycloalkyl, (C3-C7)cycloalkenyl, bicycloalkyl, bicycloalkenyl, aryl, aralkyl, heterocyclyl, heteroaryl, heterocyclyl(C1-C12)alkyl and heteroaryl(C1-C12)alkyl;
R2 represents a substituted or unsubstituted single or fused heteroaromatic or a heterocyclic group containing one or more heteroatoms selected from N, O or S;
R3 represents a group selected from the group consisting hydrogen, halo, cyano, nitro, substituted or unsubstituted(C1-C12)alkyl, substituted or unsubstituted halo(C1-C12)alkyl, hydroxyalkyl, cycloalkyl, and alkylsulfonyl X is either a bond or a group —(CH2)nN(R4)—, wherein R4 is H, or (C1-C3)alkyl and n is 0-2;
R represents —NR5R6 where R5 is either H or (C1-C6) alkyl; R6 is
where Ra is (C1-C6)alkyl or Ra forms a bridge with one of the atoms of the heterocyclic radical formed by —NRbRc;
Rb and Rc are the same or different and represent a substituted or unsubstituted group selected from alkyl, aralkyl or alkenyl or Rb and Rc together with the nitrogen atom to which they are bonded, form a 5 to 8 membered saturated or unsaturated heterocyclic radical which may be optionally substituted and may be fused;
(d) a cannabinoid receptor ligand of formula
wherein,
R7 and R8 are the same or different and represent phenyl, thienyl or pyridyl, which may be optionally substituted with 1 to 3 substituents Y, which are the same or different and are selected from the group consisting of
(C1-3)alkyl, or (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C1-2)-amino, mono- or dialkyl (C1-3)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R7 or R8 or both represent naphtyl; R9 represents a group selected from the group consisting of hydrogen, hydroxy, (C1-3)alkoxy, acetyloxy and propionyloxy;
Aa represents one of the groups (i), (ii), (iii), (iv) or (v)
wherein
R11 and R12 independently of each other represent hydrogen or branched or unbranched (C1-8)alkyl or cyclo (C3-8)alkyl; or if R11 represents acetamido, dimethylamino, 2,2,2-trifluroethyl, phenyl or pyridyl, R12 represents hydrogen;
R13 represents hydrogen or unbranched (C1-3)alkyl;
Bb represents sulfonyl or carbonyl;
R10 represents benzyl, phenyl, thienyl or pyridyl which may be substituted with 1, 2 or 3 substituents Y, which are the same or different, and are selected from the group consisting of (C1-3)alkyl, (C1-3)alkoxy, hydroxy, halogen, trifluoromethyl, trifluromethylthio, trifluromethoxy, nitro, amino, mono- or dialkyl (C12)— amino, mono- or dialkyl (C13)-alkyl sulfonyl, dimethylsulfamido, (C1-3)alkoxycarbonyl, carboxyl, trifluromethylsulfonyl, cyano, carbamoyl and acetyl; or R10 represents branched or unbranched (C1-8)alkyl or cyclo (C3-6)alkyl, or R10 represents naphthyl.
48. The compound of the formula
Patent History
Application number: 20060025448
Type: Application
Filed: Jul 20, 2005
Issued: Feb 02, 2006
Assignee:
Inventors: Braj Lohray (Ahmedabad), Vidya Lohray (Ahmedabad), Mukul Jain (Ahmedabad), Brijesh Srivastava (Ahmedabad)
Application Serial: 11/185,919
Classifications
Current U.S. Class: 514/326.000; 514/406.000
International Classification: A61K 31/454 (20060101); A61K 31/4152 (20060101);
http://patents.justia.com/patent/20060025448
http://www.google.nl/patents/EP1623741A2?cl=en
.. plus if someone wants more info but has no care to link out from icmag the info is there for them.
