发明名称 METHOD OF USING DOPAMINE REUPTAKE INHIBITORS AND THEIR ANALOGS FOR TREATING AUTOIMMUNE CONDITIONS AND DELAYING OR PREVENTING AUTOIMMUNE RELATED PATHOLOGIC PROGRESSIONS
摘要 Dopamine reuptake inhibitors, and their analogs, are disclosed for treating and delaying the progression of autoimmune diseases.
申请公布号 US2014206625(A1) 申请公布日期 2014.07.24
申请号 US201414200140 申请日期 2014.03.07
申请人 Caliper Life Sciences, Inc. 发明人 Chen Hao;Miagkov Alexei;Leary Lisa;Liu Ming;Su Qi
分类号 A61K31/4245;A61K45/06;C07D271/04 主分类号 A61K31/4245
代理机构 代理人
主权项 1. A method of providing relief from or alleviating symptoms of or delaying the progression of autoimmune disease in a patient in need of said provision of relief or alleviation of symptoms or delay of progression, the method comprising administering a therapeutically effective amount of at least one compound having the formula: wherein R1, R2, R3, R4, R5 and R6, independently of one another, are substituents selected from H, C1-C6 alkyl, OH, halogen, C5-C14 aryl, C6-C20 aralkyl, C1-C6 alkylthio, C1-C6 alkoxy, SH, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, CN, NO2, carboxy, carbalkoxy, carboxamido, alkylsulfonyl, alkylsulfonyloxy, aminosulfinyl, monoalkylaminosulfinyl, dialkylaminosulfinyl, aminosulfonyl, monoalkylaminosulfonyl, dialkylaminosulfonyl, alkylsulfonylamino, hydroxysulfonyloxy, alkoxysulfonyloxy, alkylsulfonyloxy, hydroxysulfonyl, alkoxysulfonyl, alkylsulfonylalkyl, aminosulfonylalkyl, monoalkylaminosulfonylalkyl, dialkyaminosulfonylalkyl, aminosulfinylalkyl, monoalkylaminosulfinylalkyl, dialkylaminosulfinylalkyl, said alkyl, alkenyl, alkynyl or cycloalkyl substituent being optionally substituted by at least one halogen, OH, SH, NH2, C1-C4 monoalkylamino, C1-C4 dialkylamino, COOH, CN, NO2, C1-C4 alkyl or C1-C4 alkoxy group, said aryl and aralkyl substituent being optionally substituted by at least one halogen, OH, SH, NH2, C1-C4 monoalkylamino, C1-C4 dialkylamino, COOH, CN, NO2, C1-C4 alkyl or C1-C4 alkoxy group; Ra, Rb and Rc, independently of one another, represent substituents selected from H, C1-C4 alkyl, phenyl or phenyl C1-C4 alkyl, said alkyl substituent, said phenyl substituent and said phenyl C1-C4 alkyl substituent being optionally substituted by at least one halogen, OH, SH, NH2, C1-C4 alkylmethylamino, C1-C4 dialkylamino, COOH, CN, NO2, C1-C4 alkyl or C1-C4 alkoxy group; m, n and k are independent integers from 0-4, except that m+n≠0; and the pharmaceutically acceptable salts of said compound.
地址 Hopkinton MA US