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对乙酰氨基酚及其衍生物的体外抗聚集活性。

In vitro antiaggregant activity of paracetamol and derivatives.

作者信息

Dupin J P, Gravier D, Casadebaig F, Boisseau M R, Bernard H

机构信息

Département d'Hémostase, Université de Bordeaux II, France.

出版信息

Thromb Res. 1988 May 1;50(3):437-47. doi: 10.1016/0049-3848(88)90273-3.

Abstract

The in vitro antiaggregating action of paracetamol and ten of its derivatives was studied by observing their action on collagen, adenosine-5 diphosphate (ADP) and arachidonic acid-induced platelet aggregation. It is established that in vitro activity appears not only with paracetamol but also with its positional isomers and its isosteric derivatives; this involves the replacement of oxygen by sulfur and that of the NH group of oxygen. Paracetamol and its derivatives also have an inhibiting effect on the serotonin release and the thromboxane synthesis of collagen-stimulated platelets.

摘要

通过观察对乙酰氨基酚及其十种衍生物对胶原蛋白、二磷酸腺苷(ADP)和花生四烯酸诱导的血小板聚集的作用,研究了它们的体外抗聚集作用。已确定不仅对乙酰氨基酚,而且其位置异构体和等排衍生物在体外均有活性;这涉及用硫取代氧以及用氧取代NH基团。对乙酰氨基酚及其衍生物对胶原蛋白刺激的血小板的血清素释放和血栓素合成也有抑制作用。

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