JNK Inhibitors for Treatment of Skin Diseases
This invention relates to the use of a JNK inhibitor for treating and/or preventing skin diseases selected from psoriasis and dermatitis.
1 - 18 . (canceled)
19 . A method of treating psoriasis or allergic dermatitis comprising the administration of a therapeutically effective amount of a composition comprising a JNK inhibitor to an individual in need of treatment.
20 . The method according to claim 19 , wherein the JNK inhibitor is a benzothiazole derivative according to formula (I)
tautomers, geometrical isomers, enantiomers, diastereomers, racemates and pharmaceutically acceptable salts thereof, wherein:
G is a pyrimidinyl group;
L is C 1 -C 6 -alkoxy, or an amino group, or a 3-8 membered heterocycloalkyl, containing at least one heteroatom selected from N, O, S;
R 1 is selected from the group consisting of hydrogen, sulfonyl, amino, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl or C 1 -C 6 -alkoxy, aryl, halogen, cyano and hydroxy.
21 . The method according to claim 20 , wherein R 1 is H or C 1 -C 3 alkyl.
22 . The method according to claim 20 , wherein the JNK inhibitor has formulae (Ia), (Ia′) or (Ia″):
wherein R 1 is selected from the group consisting of hydrogen, sulfonyl, amino, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl or C 1 -C 6 -alkoxy, aryl, halogen, cyano and hydroxy; L is an amino group of the formula —NR 3 R 4 wherein R 3 and R 4 are each independently from each other H, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 1 -C 6 -alkoxy, aryl, heteroaryl, saturated or unsaturated 3-8-membered cycloalkyl, 3-8-membered heterocycloalkyl, (wherein said cycloalkyl, heterocycloalkyl, aryl or heteroaryl groups may be fused with 1-2 further cycloalkyl, heterocycloalkyl, aryl or heteroaryl group), C 1 -C 6 -alkyl aryl, C 1 -C 6 -alkyl heteroaryl, C 2 -C 6 -alkenyl aryl, C 2 -C 6 -alkenyl heteroaryl, C 2 -C 6 -alkynyl aryl, C 2 -C 6 -alkynyl heteroaryl, C 1 -C 6 -alkyl cycloalkyl, C 1 -C 6 -alkyl heterocycloalkyl, C 2 -C 6 -alkenyl cycloalkyl, C 2 -C 6 -alkenyl heterocycloalkyl, C 2 -C 6 -alkynyl cycloalkyl, C 2 -C 6 -alkynyl heterocycloalkyl, or R 3 and R 4 may form a ring together with the nitrogen to which they are bound.
23 . The method according to claim 22 , wherein R 3 is hydrogen or a methyl or ethyl or propyl group and R 4 is selected from the group consisting of (C 1 -C 6 )-alkyl, C 1 -C 6 alkyl-aryl, C 1 -C 6 -alkyl-heteroaryl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl and 4-8 membered saturated or unsaturated cycloalkyl.
24 . The method according to claim 22 , wherein R 3 and R 4 form an unsubstituted or substituted piperazine or a unsubstituted or substituted piperidine or a unsubstituted or substituted morpholine or a unsubstituted or substituted pyrrolidine ring together with the nitrogen to which they are bound, whereby said substituent is selected from the group consisting of C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 1 -C 6 -alkoxy, aryl, heteroaryl, saturated or unsaturated 3-8-membered cycloalkyl, 3-8-membered heterocycloalkyl, (wherein said cycloalkyl, heterocycloalkyl, aryl or heteroaryl groups may be fused with 1-2 further cycloalkyl, heterocycloalkyl, aryl or heteroaryl group), C 1 -C 6 -alkyl aryl, C 1 -C 6 -alkyl heteroaryl, C 2 -C 6 -alkenyl aryl, C 2 -C 6 -alkenyl heteroaryl, C 2 -C 6 -alkynyl aryl, C 2 -C 6 -alkynylheteroaryl, C 1 -C 6 -alkyl cycloalkyl, C 1 -C 6 -alkyl heterocycloalkyl, C 2 -C 6 -alkenyl cycloalkyl, C 2 -C 6 -alkenyl heterocycloalkyl, C 2 -C 6 -alkynyl cycloalkyl, C 2 -C 6 -alkynyl heterocycloalkyl.
25 . The method according to claim 20 , wherein L is selected from:
wherein n is 1 to 10, preferably 1 to 6, R 5 and R 5′ are independently selected from each other from the group consisting of H, C 1 -C 10 alkyl, aryl or hetero-aryl, C 1 -C 6 alkyl-aryl and C 1 -C 6 -alkyl-heteroaryl.
26 . The method according to claim 22 , wherein L is selected from:
wherein n is 1 to 10, preferably 1 to 6, R 5 and R 5′ are independently selected from each other from the group consisting of H, C 1 -C 10 alkyl, aryl or hetero-aryl, C 1 -C 6 alkyl-aryl and C 1 -C 6 -alkyl-heteroaryl.
27 . The method according to claim 20 , wherein L is selected from:
wherein n is 1 to 10, preferably 1 to 6; and R 5 and R 5′ are independently selected from each other from the group consisting of H, C 1 -C 10 alkyl, aryl or hetero-aryl, C 1 -C 6 alkyl-aryl and C 1 -C 6 -alkyl-heteroaryl.
28 . The method according to claim 22 , wherein L is selected from:
wherein n is 1 to 10, preferably 1 to 6; and R 5 and R 5′ are independently selected from each other from the group consisting of H, C 1 -C 10 alkyl, aryl or hetero-aryl, C 1 -C 6 alkyl-aryl and C 1 -C 6 -alkyl-heteroaryl.
29 . The method according to claim 20 , wherein the JNK inhibitor is: 1,3-benzothiazol-2-yl(2-{[4-(morpholin-4-ylmethyl)benzyl]oxy}pyrimidin-4-yl)acetonitrile.
30 . The method according to claim 20 , wherein the JNK inhibitor is a compound of formula (III)
geometrical isomers, enantiomers, diastereomers, racemates and pharmaceutically acceptable salts thereof, wherein Y is a 4-12-membered saturated cyclic or bicyclic alkyl containing at least one nitrogen atom, whereby one nitrogen atom within said ring is forming a bond with the sulfonyl group of formula (III) thus providing the sulfonamide; R 1 is selected from the group consisting of hydrogen, C 1 -C 6 -alkoxy, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, amino, sulfanyl, sulfinyl, sulfonyl, sulfonyloxy, sulfonamide, acylamino, aminocarbonyl, C 1 -C 6 alkoxycarbonyl, aryl, heteroaryl, carboxy, cyano, halogen, hydroxy, nitro and hydrazide; R 2 is selected from the group consisting of hydrogen, COOR 3 , —CONR 3 R 3′ , OH, a C 1 -C 4 alkyl substituted with an OH or amino group, a hydrazido carbonyl group, a sulfate, a sulfonate, an amine and an ammonium salt; with R 3 , R 3′ being substituents independently selected from the group consisting of H, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, aryl, heteroaryl, aryl-C 1 -C 6 -alkyl, and heteroaryl-C 1 -C 6 -alkyl.
31 . The method according to claim 30 , wherein R 1 is selected from the group consisting of hydrogen, halogen, C 1 -C 6 alkyl and C 1 -C 6 alkoxy.
32 . The method according to claim 30 , wherein Y is either of the cyclic amines having the general formulae:
whereby, L 1 and L 2 are independently selected from each other from the group consisting of C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 4 -C 8 -cycloalkyl optionally containing 1-3 heteroatoms and optionally fused with aryl or heteroaryl; or L 1 and L 2 are independently selected from the group consisting of aryl, heteroaryl, aryl-C 1 -C 6 -alkyl, heteroaryl-C 1 -C 6 -alkyl, —C(O)—OR 3 , —C(O)—R 3 , —C(O)—NR 3′ R 3 , —NR 3′ R 3 , —NR 3′ C(O)R 3 , —NR 3′ C(O)NR 3′ R 3 , —(SO)R 3 , —(SO 2 )R 3 , —NSO 2 R 3 , and —SO 2 NR 3′ R 3 , with R 3 , R 3′ being substituents independently selected from the group consisting of H, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, aryl, heteroaryl, aryl-C 1 -C 6 -alkyl, and heteroaryl-C 1 -C 6 -alkyl; or L 1 and L 2 taken together form a 4-8-membered, saturated cyclic alkyl or heteroalkyl group; and R 6 is selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, OH, halogen, nitro, cyano, sulfonyl, oxo (═O), and n′ is an integer from 0 to 4, preferably 1 or 2.
33 . The method according to claim 32 , wherein R 6 is H, L 2 is H, L 1 is —NR 3′ R 3 ; where at least one of R 3′ and R 3 is not hydrogen, but a substituent selected from the group consisting of straight or branched C 4 -C 18 -alkyl, aryl-C 1 -C 18 -alkyl, heteroaryl-C 2 -C 18 -alkyl, C 1 -C 14 -alkyl substituted with a C 3 -C 12 -cycloalkyl or -bicyclo or -tricyloalkyl, and whereby said alkyl chain may contain 1-3 O or S atoms.
34 . The method according to claim 32 , wherein L 1 is —NHR 3 ; where R 3 is a straight or branched C 4 -C 12 -alkyl, preferably a C 6 -C 12 -alkyl, optionally substituted with a cyclohexyl group or a benzyl group.
35 . The method according to claim 30 , wherein Y is a piperidine group
L 1 is —NHR 3 ; where R 3 is a straight or branched C 4 -C 12 -alkyl, preferably a C 8 -C 12 -alkyl, or a benzyl group.
36 . The method according to claim 20 , wherein the JNK inhibitor is used in about 0.1 to 100 mg/kg of body weight, or about 1 to 50 mg/kg of body weight or about 5 to 10 mg/kg of body weight.
37 . The method according to claim 20 , wherein the administration of JNK inhibitor is via an oral route.
38 . The method according to claim 20 , wherein said composition further comprises an additional therapeutic agent selected from methotrexate, efalizumab, cyclosporine, corticosteroids, or topical retinoids.