Journal of Medicinal Chemistry p. 164 - 170 (1985)
Update date:2022-08-10
Topics:
Ford
Browne
Campbell
Gemenden
Goldstein
Gude
Wasley
The synthesis and structure-activity profile of a new class of potent and highly specific thromboxane A2 synthetase inhibitors is described. The most potent member of this series in vitro is determined to be imidazo[1,5-a]pyridine-5-hexanoic acid.
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Doi:10.1002/aoc.4009
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(2017)
