
Journal of Medicinal Chemistry p. 2231 - 2239 (1990)
Update date:2022-07-29
Topics:
Barraclough
Black
Cambridge
Collard
Firmin
Gerskowitch
Glen
Giles
Hill
Hull
Iyer
King
Kneen
Lindon
Nobbs
Randall
Shah
Smith
Vine
et al.
A series of 'A' ring substituted sulmazole and isomazole analogues have been prepared and evaluated as inotropic agents. pK(A)'s, protonation sites, and log P values were measured for selected compounds and their electronic properties were calculated. No simple correlation between inotropic activity and pK(A), protonation site, or log P value was observed. However, in vitro inotropism did correlate with the calculated charge density of the 'B' ring imidazo nitrogen atom. The 6-position of sulmazole appeared to be the most tolerant toward substituents, th 6-amino derivative 7 being a more potent inotrope than sulmazole itself. 4-Methoxyisomazole 13 had comparable in vivo inotropic properties to those of isomazole.
View MoreContact:86-27-84888681
Address:Wuhan economic & technology development zone
China Synchem Technology Co.,Ltd
website:http://www.cnsynchem.com
Contact:+86-0552-4929311
Address:No.217 Daqing Road
Shanghai Hohance Chemical Co., ltd
Contact:13914753421
Address:Fl.5;Bld. 70, Lane 1500; Xinfei Road
SHANGHAI SYSTEAM BIOCHEM CO., LTD
website:http://www.systeambc.com
Contact:86-021-58380978
Address:Building 87,Lane 669, Dong Jing Road Shanghai,P.R.China
Shanghai Gsyn Chemical Co.,Ltd.
Contact:86-021-67158290
Address:86-021-67158291
Doi:10.1002/jhet.5570270250
(1990)Doi:10.1007/BF00470702
(1989)Doi:10.1021/ja971774r
(1997)Doi:10.1016/S0040-4039(01)93793-1
(1989)Doi:10.1039/c0cc04660d
(2011)Doi:10.1016/j.bmcl.2010.12.064
(2011)