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通过直接作用的凝血酶抑制剂(RGH-2958)进行实验性口服抗凝治疗。

Experimental oral anticoagulation by a directly acting thrombin inhibitor (RGH-2958).

作者信息

Bagdy D, Barabás E, Fittler Z, Orbán E, Rabloczky G, Bajusz S, Széll E

机构信息

Institute for Drug Research, Budapest, Hungary.

出版信息

Folia Haematol Int Mag Klin Morphol Blutforsch. 1988;115(1-2):136-40.

PMID:2459008
Abstract

D-Phenylalanyl-L-prolyl-L-arginine aldehyde sulfate (RGH-2958), a directly acting synthetic thrombin inhibitor proved to be effective by experimental oral application. The rapid onset of its action has a special importance both from theoretical and practical point of view. Its antiplatelet effect relates to thrombin induced PA and runs parallel with the anticoagulant effect. RGH-2958 significantly reduced the thrombus weight in an experimental thrombosis model in rabbits. In the light of the therapeutic indices of the compound there is a real possibility to open a third way in the prevention and therapy of thrombosis.

摘要

D-苯丙氨酰-L-脯氨酰-L-精氨酸醛硫酸盐(RGH-2958)是一种直接作用的合成凝血酶抑制剂,经实验口服应用证明有效。从理论和实践角度来看,其作用起效迅速具有特殊重要性。其抗血小板作用与凝血酶诱导的纤溶酶原激活物(PA)有关,并与抗凝作用平行。在兔实验性血栓形成模型中,RGH-2958显著降低了血栓重量。鉴于该化合物的治疗指数,在血栓形成的预防和治疗方面确实有可能开辟第三条途径。

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