期刊
JOURNAL OF PHARMACY AND PHARMACOLOGY
卷 74, 期 6, 页码 887-895出版社
OXFORD UNIV PRESS
DOI: 10.1093/jpp/rgab075
关键词
pyranopyridine; beta-diketones; antiplatelet activity; vasodilatory; cytotoxicity; anticoagulant
资金
- EFSA-CDN project [CZ.02.1.01/0.0/0.0/16_019/0000841]
- ERDF, Charles University [SVV 260 549, 260 550]
- Science Committee of RA [20TTWS-1D009]
In this study, a series of 6-oxopyrano[3,4-c]pyridines were synthesized and the 8-methyl derivative (3a) was found to be a potent inhibitor of platelet aggregation with additional vasodilatory activity.
Objectives Both pyridine and pyrano derivatives have been previously shown to possess biologically relevant activity. In this study, we report the incorporation of these two scaffolds into one molecule. Methods The designed 3,3-dimethyl-6-oxopyrano[3,4-c]pyridines were synthesized by the acylation of enamine under Stork conditions followed by condensation of formed beta-diketones with 2-cyanoacetamide. The structures of these compounds were confirmed by using a wide spectrum of physico-chemical methods. Their antiplatelet, anticoagulant and vasodilatory activity together with toxicity were evaluated. Key findings A series of 6-oxopyrano[3,4-c]pyridines 3a-j was obtained. Four of these compounds were reported for the first time. None of the tested compounds demonstrated anticoagulant effect but 8-methyl derivative (3a) was a potent antiplatelet compound with IC50 numerically twice as low as the clinically used acetylsalicylic acid. A series of further mechanistic tests showed that 3a interferes with calcium signaling. The compound is also not toxic and in addition possesses vasodilatory activity as well. Conclusions Compound 3a is a promising inhibitor of platelet aggregation, whose mechanism of action should be studied in detail.
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