ARYL SULFONAMIDES
Compounds are provided that act as potent antagonists of the CCR9 receptor, and which have been further confirmed in animal testing for inflammation, one of the hallmark disease states for CCR9. The compounds are generally aryl sulfonamide derivatives and are useful in pharmaceutical compositions, methods for the treatment of CCR9-mediated diseases, and as controls in assays for the identification of CCR9 antagonists.
1 - 10 . (canceled)
11 . A compound of the formula (I), or a salt thereof:
where
X represents from 1 to 4 substituents independently selected from the group consisting of halogen, —CN, —NO 2 , —OH, —OR 1 , —C(O)R 1 , —CO 2 R 1 , —O(CO)R 1 , —C(O)NR 1 R 2 , —OC(O)NR 1 R 2 , —SR', —SOR 1 , —SO 2 R 1 , —SO 2 NR 1 R 2 , —NR 1 R 2 , —NR 1 C(O)R 2 , —NR 1 C(O) 2 R 2 , —NR 1 SO 2 R 2 , —NR 1 (CO)NR 2 R 3 , unsubstituted or substituted C 1-8 alkyl, unsubstituted or substituted C 2-8 alkenyl, unsubstituted or substituted C 2-8 alkynyl, unsubstituted or substituted C 3-8 cycloalkyl, unsubstituted or substituted C 6-10 aryl, unsubstituted or substituted 5- to 10-membered heteroaryl, and unsubstituted or substituted 3- to 10-membered heterocyclyl;
R 1 , R 2 and R 3 are each independently selected from the group consisting of hydrogen, unsubstituted or substituted C 1-6 haloalkyl, unsubstituted or substituted C 1-6 alkyl, unsubstituted or substituted C 3-6 cycloalkyl, unsubstituted or substituted C 2-6 alkenyl, unsubstituted or substituted C 2-6 alkynyl, unsubstituted or substituted C 6-10 aryl, unsubstituted or substituted 5- to 10-membered heteroaryl, unsubstituted or substituted aryl-C 1-4 alkyl, unsubstituted or substituted aryl-C 1-4 alkyl, and unsubstituted or substituted aryloxy-C 1-4 alkyl; or
two of R 1 , R 2 and R 3 together with the atom(s) to which they are attached, may form an unsubstituted or substituted 5-, 6- or 7-membered ring;
Y represents from 1 to 3 substituents, each independently selected from the group consisting of halogen, —CN, —NO 2 , —OH, —OR 4 , —C(O)R 4 , —CO 2 R 4 , —SR 4 , —SOR 4 , —SO 2 R 4 , and unsubstituted or substituted C 1-4 alkyl;
R 4 is selected from the group consisting of hydrogen, unsubstituted or substituted C 1-6 haloalkyl, unsubstituted or substituted C 1-6 alkyl, unsubstituted or substituted C 3-6 cycloalkyl, unsubstituted or substituted C 2-6 alkenyl, and unsubstituted or substituted C 2-6 alkynyl;
L is —C(O)—, —S—, —SO— or —S(O) 2 —; and
Z represents either unsubstituted or substituted monocyclic or bicyclic C 5-10 heteroaryl or unsubstituted or substituted monocyclic or bicyclic C 3-10 heterocyclyl,
with the proviso that when X is methyl, then Z is not 2-thiophene, 2-(3-hydroxy-1H-indole) or 3-(1-methylpyridinium).
12 . The compound of claim 11 , where L is —CO—.
13 . A composition comprising a pharmaceutically acceptable carrier and a compound of claim 11 .
14 . A method for treating a CCR9-mediated condition or disease comprising administering to a subject a safe and effective amount of a compound of the formula (I), or a salt thereof:
where
X represents from 1 to 4 substituents independently selected from the group consisting of halogen, —CN, —NO 2 , —OH, —OR 1 , —C(O)R 1 , —CO 2 R 1 , —O(CO)R 1 , —C(O)NR 1 R 2 , —OC(O)NR 1 R 2 , —SR 1 , —SOR 1 , —SO 2 R 1 , —SO 2 NR 1 R 2 , —NR 1 R 2 , —NR 1 C(O)R 2 , —NR 1 C(O) 2 R 2 , —NR 1 SO 2 R 2 , —NR 1 (CO)NR 2 R 3 , unsubstituted or substituted C 1-8 alkyl, unsubstituted or substituted C 2-8 alkenyl, unsubstituted or substituted C 2-8 alkynyl, unsubstituted or substituted C 3-8 cycloalkyl, unsubstituted or substituted C 6-10 aryl, unsubstituted or substituted 5- to 10-membered heteroaryl, and unsubstituted or substituted 3- to 10-membered heterocyclyl;
R 1 , R 2 and R 3 are each independently selected from the group consisting of hydrogen, unsubstituted or substituted C 1-6 haloalkyl, unsubstituted or substituted C 1-6 alkyl, unsubstituted or substituted C 3-6 cycloalkyl, unsubstituted or substituted C 2-6 alkenyl, unsubstituted or substituted C 2-6 alkynyl, unsubstituted or substituted C 6-10 aryl, unsubstituted or substituted 5- to 10-membered heteroaryl, unsubstituted or substituted aryl-C 1-4 alkyl, unsubstituted or substituted aryl-C 1-4 alkyl, and unsubstituted or substituted aryloxy-C 1-4 alkyl; or
two of R 1 , R 2 and R 3 together with the atom(s) to which they are attached, may form an unsubstituted or substituted 5-, 6- or 7-membered ring;
Y represents from 1 to 3 substituents, each independently selected from the group consisting of halogen, —CN, —NO 2 , —OH, —OR 4 , —C(O)R 4 , —CO 2 R 4 , —SR 4 , —SOR 4 , —SO 2 R 4 , and unsubstituted or substituted C 1-4 alkyl;
R 4 is selected from the group consisting of hydrogen, unsubstituted or substituted C 1-6 haloalkyl, unsubstituted or substituted C 1-6 alkyl, unsubstituted or substituted C 3-6 cycloalkyl, unsubstituted or substituted C 2-6 alkenyl, and unsubstituted or substituted C 2-6 alkynyl;
L is —C(O)—; and
Z represents either unsubstituted or substituted monocyclic or bicyclic C 5-10 heteroaryl or unsubstituted or substituted monocyclic or bicyclic C 3-10 heterocyclyl,
with the proviso that when X is methyl, then Z is not 2-thiophene, 2-(3-hydroxy-1H-indole) or 3-(1-methylpyridinium).
15 . The method of claim 14 , where the CCR9-mediated disease or condition is an inflammatory condition.
16 . The method of claim 14 , where the CCR9-mediated disease or condition is an immunoregulatory disorder.
17 . The method of claim 14 , where the CCR9-mediated condition or disease is inflammatory bowel disease.
18 . The method of claim 14 , where the CCR9-mediated condition or disease is selected from the group consisting of an allergic disease, psoriasis, atopic dermatitis, asthma, fibrotic diseases and graft rejection.
19 . The method of claim 14 , where the CCR9-mediated condition or disease is selected from the group consisting of immune mediated food allergies and autoimmune diseases.
20 . The method of claim 14 , where the CCR9-mediated condition or disease is Celiac disease or rheumatoid arthritis.
21 . The method of claim 14 , where the administering is oral, parenteral, rectal, transdermal, sublingual, nasal or topical.
22 . The method of claim 14 , where the compound is administered in combination with an anti-inflammatory or analgesic agent.
23 . The method of claim 14 , where the CCR9-mediated disease or condition is leukemia or a solid tumor.
24 . The method of claim 14 , where the CCR9-mediated disease or condition is thymoma or a thymic carcinoma.
25 . The method of claim 14 , where the CCR9-mediated disease or condition is acute lymphocytic leukemia.
26 . A method of modulating CCR9 function in a cell, comprising contacting the cell with a CCR9 modulating amount of a compound of the formula (I), or a salt thereof:
where
X represents from 1 to 4 substituents independently selected from the group consisting of halogen, —CN, —NO 2 , —OH, —OR 1 , —C(O)R 1 , —CO 2 R 1 , —O(CO)R 1 , —C(O)NR 1 R 2 , —OC(O)NR 1 R 2 , —SR 1 , —SOR 1 , —SO 2 R 1 , —SO 2 NR 1 R 2 , —NR 1 R 2 , —NR 1 C(O)R 2 , —NR 1 C(O) 2 R 2 , —NR 1 SO 2 R 2 , —NR 1 (CO)NR 2 R 3 , unsubstituted or substituted C 1-8 alkyl, unsubstituted or substituted C 2-8 alkenyl, unsubstituted or substituted C 2-8 alkynyl, unsubstituted or substituted C 3-8 cycloalkyl, unsubstituted or substituted C 6-10 aryl, unsubstituted or substituted 5- to 10-membered heteroaryl, and unsubstituted or substituted 3- to 10-membered heterocyclyl;
R 1 , R 2 and R 3 are each independently selected from the group consisting of hydrogen, unsubstituted or substituted C 1-6 haloalkyl, unsubstituted or substituted C 1-6 alkyl, unsubstituted or substituted C 3-6 cycloalkyl, unsubstituted or substituted C 2-6 alkenyl, unsubstituted or substituted C 2-6 alkynyl, unsubstituted or substituted C 6-10 aryl, unsubstituted or substituted 5- to 10-membered heteroaryl, unsubstituted or substituted aryl-C 1-4 alkyl, unsubstituted or substituted aryl-C 1-4 alkyl, and unsubstituted or substituted aryloxy-C 1-4 alkyl; or
two of R 1 , R 2 and R 3 together with the atom(s) to which they are attached, may form an unsubstituted or substituted 5-, 6- or 7-membered ring;
Y represents from 1 to 3 substituents, each independently selected from the group consisting of halogen, —CN, —NO 2 , —OH, —OR 4 , —C(O)R 4 , —CO 2 R 4 , —SR 4 , —SOR 4 , —SO 2 R 4 , and unsubstituted or substituted C 1-4 alkyl;
R 4 is selected from the group consisting of hydrogen, unsubstituted or substituted C 1-6 haloalkyl, unsubstituted or substituted C 1-6 alkyl, unsubstituted or substituted C 3-6 cycloalkyl, unsubstituted or substituted C 2-6 alkenyl, and unsubstituted or substituted C 2-6 alkynyl;
L is —C(O)—; and
Z represents either unsubstituted or substituted monocyclic or bicyclic C 5-10 heteroaryl or unsubstituted or substituted monocyclic or bicyclic C 3-10 heterocyclyl,
with the proviso that when X is methyl, then Z is not 2-thiophene, 2-(3-hydroxy-1H-indole) or 3-(1-methylpyridinium).