作者:C. Altomare、L. Summo、S. Cellamare、A.V. Varlamov、L.G. Voskressensky、T.N. Borisova、A. Carotti
DOI:10.1016/s0960-894x(00)00052-4
日期:2000.3
A series of pyrrolo[3,2-c]pyridines, isosteres of the antithrombotic drug ticlopidine, has been synthesized and evaluated in vitro for the ability to inhibit aggregation of human platelet-rich plasma induced by adenosin 5'-diphosphate (ADP). Structure-activity relationships showed their antiplatelet effects to be related to the lipophilicity.
已经合成了一系列吡咯并[3,2-c]吡啶,即抗血栓药物噻氯匹定的等排物,并在体外评估了抑制人腺苷5'-二磷酸(ADP)诱导的富含血小板的血浆聚集的能力。构效关系表明它们的抗血小板作用与亲脂性有关。