Inhibition of platelet aggregation by novel triphenylethylene analogs.

Abstract:

:The present study has evaluated the effect of some newly synthesized triphenylethylene (TPE) analogs on platelet arachidonic acid metabolism and function. All compounds tested inhibited arachidonic acid induced platelet aggregation and several were superior to aspirin in their relative potency. Introduction of a carboxyl function into the alpha-ring, which should enhance binding according to proposed structural models for cyclooxygenase inhibitors, was not found to be beneficial. Increased structural rigidity, which resulted from covalent linkage of two aromatic rings in this series, did not eliminate anti-aggregatory properties.

journal_name

Thromb Res

journal_title

Thrombosis research

authors

Rao GH,John V,Hill TD,Vennerstrom JL,White JG,Holmes TJ Jr

doi

10.1016/0049-3848(86)90330-0

subject

Has Abstract

pub_date

1986-11-15 00:00:00

pages

527-38

issue

4

eissn

0049-3848

issn

1879-2472

journal_volume

44

pub_type

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