发明名称 |
PHARMACEUTICAL COMPOSITION COMPRISING N1-CYCLIC AMINE-N5-SUBSTITUTED BIGUANIDE DERIVATIVES AS AN INGREDIENT FOR PREVENTING OR TREATING FIBROSIS |
摘要 |
The present invention provides a novel use of N1-cyclic amine-N5-substituted biguanide derivatives for preparing a medicine for preventing or treating fibrosis. The N1-cyclic amine-N5-substituted biguanide derivatives according to the present invention are capable of effectively inhibiting fibrosis by effectively suppressing the EMT. |
申请公布号 |
US2016101112(A1) |
申请公布日期 |
2016.04.14 |
申请号 |
US201414893433 |
申请日期 |
2014.05.20 |
申请人 |
IMMUNOMET THERAPEUTICS INC |
发明人 |
Kim Sung Wuk;Lee Soon Im;Song Yeon Jung;Shin Min Jae;Oh Kook Hwan;Ju Kyung Don;Shin Eun Kyoung;Lee Ji Sun;Heo Hye Jin;Lee Hong Bum;Kook Ji Ae;Kim Min Jeong;Eum Hye Soun |
分类号 |
A61K31/55;A61K31/44;A61K31/397;A61K31/445;A61K31/40 |
主分类号 |
A61K31/55 |
代理机构 |
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代理人 |
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主权项 |
1. A method of preventing or treating fibrosis comprising administering a therapeutically effective amount of a N1-cyclic amine-N5-substituted biguanide derivative compound of Formula 1 below or a pharmaceutically acceptable salt thereof to a subject in need thereof: wherein R1 and R2 are taken together with nitrogen to which they are attached to form 4- to 7-membered C3-6 heterocycloalkyl or C3-6 heterocycloalkene; R3 is H; C3-7 cycloalkyl; C3-12 aryl; or C1-6 alkyl unsubstituted or substituted with C3-12 aryl or C3-12 heteroaryl; wherein C3-6 heterocycloalkyl, cycloalkyl, C3-12 aryl, or C3-12 heteroaryl is unsubstituted or substituted with at least one non-hydrogen substituent selected from the group consisting of halogen, C1-4 alkyl, and C1-4 alkoxy, and the non-hydrogen substituent is unsubstituted or further substituted with halogen. |
地址 |
Cambridge MA US |