发明名称 Tricyclic fused heterocyclic compound, process for preparing it and medicament comprising it
摘要 The present invention provides a novel compound having an excellent corticotrophin-releasing-factor receptor antagonistic activity. That is, it provides a compound represented by the following formula, a pharmacologically acceptable salt thereof or hydrates thereof. Wherein A, B and D are the same as or different from each other and each represents a group represented by the formula -(CR<1>R<2>)m- (wherein R<1 >and R<2 >are the same as or different from each other and each represents a C1-6 alkyl group etc.), -NR<3>- (wherein R<3 >represetns hydrogen etc.) etc.; E and G are the same as or different from each other and each represents a group represented by the formula -(CR<6>R<7>)p- (wherein R<6 >and R<7 >are the same as or different from each other and each represents hydrogen etc.; and p represents an integer of 0, 1 or 2); J represents a carbon atom or nitrogen atom, each substituted with C1-6 alkyl group optionally substituted with a halogen atom, etc.; K and L are the same as or different from each other and each represents carbon atom or nitrogen atom; M means hydrogen, a halogen atom, an optionally substituted C1-6 alkyl group etc.; and the partial structure means a single or double bond.
申请公布号 US2005004147(A1) 申请公布日期 2005.01.06
申请号 US20040903059 申请日期 2004.08.02
申请人 EISAI CO., LTD. 发明人 HIBI SHIGEKI;HOSHINO YORIHISA;YOSHIUCHI TATSUYA;SHIN KOGYOKU;KIKUCHI KOUICHI;SOEJIMA MOTOHIRO;TABATA MUTSUKO;TAKAHASHI YOSHINORI;SHIBATA HISASHI;HIDA TAKAYUKI;HIRAKAWA TETSUYA;INO MITSUHIRO
分类号 A61P1/04;A61P1/08;A61P1/10;A61P1/12;A61P1/14;A61P9/04;A61P9/10;A61P9/12;A61P11/00;C07D471/14;C07D487/14;C07D491/14;(IPC1-7):A61K31/519 主分类号 A61P1/04
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