Abstract
A series of aryl- or aralky-substituted 2-amino-3,4-dihydroquinazolines and related compounds were synthesized. The compounds were evaluated for inhibitory activity towards collagen- and ADP-induced aggregation of rat blood platelet in vitro and ex vivo. A group of 3-benzyl-substituted derivatives had potent activity. The structure-activity relationships are discussed. © 1980, The Pharmaceutical Society of Japan. All rights reserved.
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Ishikawa, F., Watanabe, Y., & Saegusa, J. (1980). Cyclic Guanidines. IX. Synthesis of 2-Amino-3,4-dihydroquinazolines as Blood Platelet Aggregation Inhibitors. Chemical and Pharmaceutical Bulletin, 28(5), 1357–1364. https://doi.org/10.1248/cpb.28.1357
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