Structure-activity relationships for selected sulfur-rich antithrombotic compounds

Citation
Ja. Macdonald et Rf. Langler, Structure-activity relationships for selected sulfur-rich antithrombotic compounds, BIOC BIOP R, 273(2), 2000, pp. 421-424
Citations number
20
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ISSN journal
0006291X → ACNP
Volume
273
Issue
2
Year of publication
2000
Pages
421 - 424
Database
ISI
SICI code
0006-291X(20000705)273:2<421:SRFSSA>2.0.ZU;2-G
Abstract
We assessed the antithrombotic activity of some simple organosulfur compoun ds which have some of the functionality found in the disulfide ajoene, a ph armacologically active compound isolated from garlic. The results establish that antithrombotic activity is associated with disulfides directly attach ed to a phenyl ring and is further enhanced by an alpha-sulfonyl group. CH3 SO2CH2SSPh proved to be a potent inhibitor of platelet aggregation with an IC50 of 5 mu M. (C) 2000 Academic Press.