Synthesis and platelet aggregation inhibitory activity of 4,5-bis(substituted)-1,2,3-thiadiazoles
作者:Edward W. Thomas、Edward E. Nishizawa、David C. Zimmermann、Davey J. Williams
DOI:10.1021/jm00382a009
日期:1985.4
Routine screening of compounds for inhibition of collagen-induced platelet aggregation in vitro revealed 4,5-bis-(4-methoxyphenyl)-1,2,3-thiadiazole (2) was active and it represents the first example of a 1,2,3-thiadiazole with possible antithrombotic activity. In order to develop a structure-activity relationship for this heterocycle, a number of new 4(5)-mono- and -disubstituted 1,2,3-thiadiazoles were synthesized. These were tested in our screen and a number of additional active compounds were found. The most active compounds (2, 5a, 5b, and 6c) were those in which the heterocycle was substituted with benzene rings possessing para electron-donating groups.
Zimmer, Oswald; Echter, Toni; Merkle, Ursula, Liebigs Annalen der Chemie, 1982, # 4, p. 683 - 698
作者:Zimmer, Oswald、Echter, Toni、Merkle, Ursula、Meier, Herbert
DOI:——
日期:——
ZIMMER, O.;ECHTER, T.;MERKLE, U.;MEIER, H., LIEBIGS ANN. CHEM., 1982, N 4, 683-698
作者:ZIMMER, O.、ECHTER, T.、MERKLE, U.、MEIER, H.
DOI:——
日期:——
THOMAS, E. W.;NISHIZAWA, E. E.;ZIMMERMANN, D. C.;WILLIAMS, D. J., J. MED. CHEM., 1985, 28, N 4, 442-446
作者:THOMAS, E. W.、NISHIZAWA, E. E.、ZIMMERMANN, D. C.、WILLIAMS, D. J.
DOI:——
日期:——
Redlich, Hartmut, Liebigs Annalen der Chemie, 1982, # 4, p. 708 - 716