发明名称 N-PHENPROPYLCYCLOPENTYL-SUBSTITUTED GLUTARAMIDE DERIVATIVES AS NEP INHIBITORS FOR FSAD.
摘要 <p>The invention relates to compounds of formula (I) for treating for example sexual dysfunction, wherein R1 is optionally substituted C1-6alkyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, hydrogen, C1-6alkoxy, -NR2 R3 or - NR4SO2R5; X is the linkage -(CH2)n- or -(CH2)q-O- (wherein Y is attached to the oxygen); wherein one or more hydrogen atoms in linkage X may be replaced independently by C1-4alkoxy; hydroxy; hydroxy(C1-3alkyl); C3-7cycloalkyl; carbocyclyl; heterocyclyl; or by C1-4alkyl optionally substituted by one or more fluoro or phenyl groups; n is 3, 4, 5, 6, or 7; and q is 2, 3, 4, 5 or 6; and Y is phenyl or pyridyl, each of which may be substituted; or two R8 groups on adjacent carbon atoms together with the interconnecting carbon atoms may form a fused optionally substituted 5- or 6-membered carbocyclic or heterocyclyic ring.</p>
申请公布号 MXPA03006597(A) 申请公布日期 2004.10.15
申请号 MX2003PA06597 申请日期 2002.03.18
申请人 PFIZER INC. 发明人 DAVID CAMERON PRYDE
分类号 C07D317/46;A61K;A61K31/165;A61K31/195;A61K31/277;A61K31/335;A61K31/343;A61K31/353;A61K31/357;A61K31/36;A61K31/40;A61K31/41;A61K31/416;A61K31/435;A61K31/4402;A61K31/4535;A61K31/47;A61K31/519;A61K31/565;A61K31/566;A61K31/568;A61K45/00;A61P;A61P15/00;A61P15/10;A61P43/00;C07C;C07C233/58;C07C233/59;C07C233/60;C07C235/40;C07C235/82;C07C255/60;C07C323/40;C07D;C07D213/40;C07D215/12;C07D231/56;C07D307/79;C07D307/81;C07D311/58;C07D311/74;C07D317/52;C07D317/62;C07D319/18;C07D319/20;(IPC1-7):A61K31/195 主分类号 C07D317/46
代理机构 代理人
主权项
地址