A series of pyrrolo[3,2-c]pyridines, isosteres of the antithrombotic drug t
iclopidine, has been synthesized and evaluated in vitro for the ability to
inhibit aggregation of human platelet-rich plasma induced by adenosin 5'-di
phosphate (ADP). Structure-activity relationships showed their antiplatelet
effects to be related to the Lipophilicity. (C) 2000 Elsevier Science Ltd.
All rights reserved.