| Literature DB >> 4198692 |
R G McDonald-Gibson, J D Flack, P W Ramwell.
Abstract
Some oxaprostaglandin derivatives have been shown to inhibit prostaglandin biosynthesis from arachidonate by a particulate prostaglandin synthetase preparation. The most potent inhibitor was 5-oxaprost-13-trans-enoate, and inhibition by this compound appeared to be competitive. Certain structure-activity relationships were ascertained.Entities:
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Year: 1973 PMID: 4198692 PMCID: PMC1177566 DOI: 10.1042/bj1320117
Source DB: PubMed Journal: Biochem J ISSN: 0264-6021 Impact factor: 3.857