ALKYL SUBSTITUTED INDOLOQUINOXALINES
    1.
    发明申请
    ALKYL SUBSTITUTED INDOLOQUINOXALINES 有权
    烷基取代的吲哚啉酮

    公开(公告)号:US20100009999A1

    公开(公告)日:2010-01-14

    申请号:US12496261

    申请日:2009-07-01

    IPC分类号: A61K31/4985

    CPC分类号: C07D487/04

    摘要: Novel substituted indoloquinoxalines of formula (I wherein R1 is hydrogen or represents one or more similar or different substituents in the positions 7 to 10 selected from the group halogen, lower alkyl/alkoxy, hydroxy, trifluoromethyl, trichloromethyl, trifluoromethoxy, R2 represents similar or different C1-C4 alkyl substituents, X is CO or CH2, Y is OH, NH2, NH—(CH2)n—R3 wherein R3 represents lower alkyl, OH, NH2, NHR4 or NR5R6 wherein R4, R5 and R6 independently are lower alkyl or cyclo-alkyl and n is an integer of from 2 to 4, with the provision that when X is CH2, Y is OH or NH—(CH2)n—OH, and pharmacologically acceptable salts thereof are described. The compounds are useful as drugs for preventing and/or treating autoimmune diseases.

    摘要翻译: 式(I的新型取代吲哚并喹啉,其中R 1为氢或表示选自卤素,低级烷基/烷氧基,羟基,三氟甲基,三氯甲基,三氟甲氧基,R 2中的7至10位的一个或多个相似或不同的取代基表示相似或不同的 C 1 -C 4烷基取代基,X是CO或CH 2,Y是OH,NH 2,NH-(CH 2)n -R 3,其中R 3表示低级烷基,OH,NH 2,NHR 4或NR 5 R 6,其中R 4,R 5和R 6独立地是低级烷基或 环烷基,n为2〜4的整数,条件是当X为CH 2时,Y为OH或NH-(CH 2)n -OH,并描述其药理学上可接受的盐,该化合物可用作药物 用于预防和/或治疗自身免疫性疾病。

    ALKYL SUBSTITUTED INDOLOQUINOXALINES
    2.
    发明申请
    ALKYL SUBSTITUTED INDOLOQUINOXALINES 有权
    烷基取代的吲哚啉酮

    公开(公告)号:US20110086859A9

    公开(公告)日:2011-04-14

    申请号:US12496261

    申请日:2009-07-01

    IPC分类号: A61K31/4985

    CPC分类号: C07D487/04

    摘要: Novel substituted indoloquinoxalines of formula (I wherein R1 is hydrogen or represents one or more similar or different substituents in the positions 7 to 10 selected from the group halogen, lower alkyl/alkoxy, hydroxy, trifluoromethyl, trichloromethyl, trifluoromethoxy, R2 represents similar or different C1-C4 alkyl substituents, X is CO or CH2, Y is OH, NH2, NH—(CH2)n—R3 wherein R3 represents lower alkyl, OH, NH2, NHR4 or NR5R6 wherein R4, R5 and R6 independently are lower alkyl or cyclo-alkyl and n is an integer of from 2 to 4, with the provision that when X is CH2, Y is OH or NH—(CH2)n—OH, and pharmacologically acceptable salts thereof are described. The compounds are useful as drugs for preventing and/or treating autoimmune diseases.

    摘要翻译: 式(I的新型取代吲哚并喹啉,其中R 1为氢或表示选自卤素,低级烷基/烷氧基,羟基,三氟甲基,三氯甲基,三氟甲氧基,R 2中的7至10位的一个或多个相似或不同的取代基表示相似或不同的 C 1 -C 4烷基取代基,X是CO或CH 2,Y是OH,NH 2,NH-(CH 2)n -R 3,其中R 3表示低级烷基,OH,NH 2,NHR 4或NR 5 R 6,其中R 4,R 5和R 6独立地是低级烷基或 环烷基,n为2〜4的整数,条件是当X为CH 2时,Y为OH或NH-(CH 2)n -OH,并描述其药理学上可接受的盐,该化合物可用作药物 用于预防和/或治疗自身免疫性疾病。

    Alkyl substituted indoloquinoxalines
    3.
    发明申请
    Alkyl substituted indoloquinoxalines 有权
    烷基取代的吲哚并噻嗪

    公开(公告)号:US20050288296A1

    公开(公告)日:2005-12-29

    申请号:US11143935

    申请日:2005-09-08

    CPC分类号: C07D487/04

    摘要: Novel substituted indoloquinoxalines of formula (I wherein R1 is hydrogen or represents one or more similar or different substituents in the positions 7 to 10 selected from the group halogen, lower alkyl/alkoxy, hydroxy, trifluoromethyl, trichloromethyl, trifluoromethoxy, R2 represents similar or different C1-C4 alkyl substituents, X is CO or CH2, Y is OH, NH2, NH—(CH2)n—R3 wherein R3 represents lower alkyl, OH, NH2, NHR4 or NR5R6 wherein R4, R5 and R6 independently are lower alkyl or cyclo-alkyl and n is an integer of from 2 to 4, with the provision that when X is CH2, Y is OH or NH—(CH2)n—OH, and pharmacologically acceptable salts thereof are described. The compounds are useful as drugs for preventing and/or treating autoimmune diseases.

    摘要翻译: 式(I)的新型取代吲哚并喹啉,其中R 1是氢或表示选自卤素,低级烷基/烷氧基,羟基,三氟甲基,三氯甲基的7至10位中的一个或多个相似或不同的取代基 ,三氟甲氧基,R 2表示相似或不同的C 1 -C 4烷基取代基,X为CO或CH 2 >,Y是OH,NH 2,NH-(CH 2 CH 2)n -R 3其中R' SO 3表示低级烷基,OH,NH 2,NHR 4或NR 5 R 6 O / 其中R 4,R 5和R 6独立地是低级烷基或环烷基,n是2至4的整数, 其条件是当X是CH 2时,Y是OH或NH-(CH 2)n -OH)及其药理学上可接受的盐 这些化合物可用作预防和/或治疗自身免疫性疾病的药物。

    Alkyl substituted indoloquinoxalines
    4.
    发明授权
    Alkyl substituted indoloquinoxalines 有权
    烷基取代的吲哚并噻嗪

    公开(公告)号:US07589093B2

    公开(公告)日:2009-09-15

    申请号:US11143935

    申请日:2005-06-03

    CPC分类号: C07D487/04

    摘要: Novel substituted indoloquinoxalines of formula wherein R1 is hydrogen or represents one or more similar or different substituents in the positions 7 to 10 selected from the group halogen, lower alkyl/alkoxy, hydroxy, trifluoromethyl, trichloromethyl, trifluoromethoxy, R2 represents similar or different C1-C4 alkyl substituents, X is CO or CH2, Y is OH, NH2, NH—(CH2)n—R3 wherein R3 represents lower alkyl, OH, NH2, NHR4 or NR5R6 wherein R4, R5 and R6 independently are lower alkyl or cyclo-alkyl and n is an integer of from 2 to 4, with the provision that when X is CH2, Y is OH or NH—(CH2)n—OH, and pharmacologically acceptable salts thereof are described. The compounds are useful as drugs for preventing and/or treating autoimmune diseases.

    摘要翻译: 低级烷基/烷氧基,羟基,三氟甲基,三氯甲基,三氟甲氧基,R 2表示相同或不同的C1-4烷基的新颖取代吲哚并喹啉,其中R 1为氢或表示选自卤素,低级烷氧基,羟基,三氟甲基,三氯甲基,三氟甲氧基的7至10位中的一个或多个相似或不同的取代基, C4烷基取代基,X是CO或CH2,Y是OH,NH2,NH-(CH2)n-R3,其中R3代表低级烷基,OH,NH2,NHR4或NR5R6,其中R4,R5和R6独立地是低级烷基或环 - 烷基,n是2至4的整数,条件是当X是CH 2时,Y是OH或NH-(CH 2)n -OH,并且其药理学上可接受的盐被描述。 该化合物可用作预防和/或治疗自身免疫性疾病的药物。