Chemical and Pharmaceutical Bulletin p. 1151 - 1157 (1983)
Update date:2022-08-04
Topics:
Nishi
Tabusa
Tanaka
Shimizu
Kanbe
Kimura
Nakagawa
A series of ω-(1-substituted-5-tetrazolylalkoxy)-2-oxoquinolines was synthesized and tested for inhibitory activity towards collagen- and adenosine diphosphate (ADP)-induced aggregation of rabbit blood platelets in vitro. These compounds were prepared by the reaction of 1-substituted-5-(ω-chloroalkyl)-tetrazoles and hydroxy-2-oxoquinolines in the presence of a base. Among them, 6-[3-(1-cyclohexyl-5-tetrazolyl)propoxy]-1,2-dihydro-2-oxoquinoline (IVb) was found to have the most potent inhibitory activity. The structure-activity relationships are discussed.
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Doi:10.1016/S0040-4039(01)92934-X
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