Spirocyclic nonpeptide glycoprotein IIb–IIIa antagonists. Part 3: synthesis and SAR of potent and specific 2,8-diazaspiro[4.5]decanes
作者:Mukund M. Mehrotra、Julie A. Heath、Jack W. Rose、Mark S. Smyth、Joseph Seroogy、Deborah L. Volkots、Gerd Ruhter、Theo Schotten、Lisa Alaimo、Gary Park、Anjali Pandey、Robert M. Scarborough
DOI:10.1016/s0960-894x(02)00095-1
日期:2002.4
The synthesis and biological activity of analogues containing spiro piperidinylpyridine and pyrrolidinylpyridine templates are described. The potent activity of these compounds as platelet aggregation inhibitors demonstrates the utility of the spiro structures as central template for nonpeptide RGD mimics. (C) 2002 Elsevier Science Ltd. All rights reserved.
PYRIDYL-CONTAINING SPIROCYCLIC COMPOUNDS AS INHIBITORS OF FIBRINOGEN-DEPENDENT PLATELET AGGREGATION
申请人:Millennium Pharmaceuticals, Inc.
公开号:EP1224186B1
公开(公告)日:2003-09-24
[EN] PYRIDYL-CONTAINING SPIROCYCLIC COMPOUNDS AS INHIBITORS OF FIBRINOGEN-DEPENDENT PLATELET AGGREGATION<br/>[FR] COMPOSES SPIROCYCLIQUES PYRIDILES INHIBITEURS DE L'AGREGATION PLAQUETTAIRE DEPENDANT DES FIBRINOGENES
申请人:COR THERAPEUTICS INC
公开号:WO2001030780A2
公开(公告)日:2001-05-03
This invention relates to certain substituted or unsubstituted pyridyl-containing spirocyclic compounds substituted with both basic and acidic functionality, which are useful in inhibition of platelet aggregation.