发明名称 NEW CONDENSED CYCLIC COMPOUND OR ITS SALT AND ITS MEDICINAL USE
摘要 <p>PURPOSE:To obtain a low toxic new condensed cyclic compound having excellent glycoprotein GPIIb/III antagonistic activity, capable of oral administration, long in blood life, having low side effects, thus useful for preventing and treating thrombosis etc. CONSTITUTION:This condensed cyclic compound (or a pharmacologically permissible salt thereof) is represented by formula I {A is of formula II, III or IV (E is H, amidino, guanidino or an amino protecting group; (e) is 0-3); B is of formula V, VI, VII or VIII [D is of formula IX (Q is 0 or NR<6>; (g) is O or 1; (h) is 0-3); (m) is 0 or 1; (n) is 1 or 2; (f) is 1-3]; R<1> to R<4> are each H, a lower alkyl, a halogen, an acyl or an alkoxyl; R<5> is H, a lower alkyl, a cycloalkyl or an aralkyl; R<6> is H, a lower alkyl or an aralkyl; G is CH or N; L and M are each O or NR<6>; (a) and (c) are each 0 or 1; (b) and (d) are each 0-3}, e.g. 2-amidino-6-{[(4-methoxycarbonylcyc-lohexyl) aminocarbonyl]methoxy}naphthalene.</p>
申请公布号 JPH07179407(A) 申请公布日期 1995.07.18
申请号 JP19940278180 申请日期 1994.11.11
申请人 GREEN CROSS CORP:THE 发明人 ASHIMORI ATSUYUKI;YOSHIDA TOMOHIRO;ONO SHINICHIROU;EDA MASAHIRO;KOSAKA KEIGO;MORI FUMIO;INOUE YOSHIHISA;IMADA MITSUAKI;IKEGAWA RURIKO;OU HOU;NAKAMURA NORIFUMI
分类号 C07D215/48;A61K31/135;A61K31/155;A61K31/165;A61K31/215;A61K31/445;A61K31/47;A61K31/495;A61P7/02;C07C217/84;C07C229/34;C07C229/42;C07C237/06;C07C257/18;C07C279/18;C07D211/34;C07D211/44;C07D241/04;(IPC1-7):C07C229/42 主分类号 C07D215/48
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