
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 MoreMelone Pharmaceutical Co., ltd
Contact:+86-411 82593920, 82593631
Address:No 232, JInma Roda, Development Zone, Dalian, China
HENAN NEW BLUE CHEMICAL CO.,LTD
website:http://www.newbluechem.com
Contact:86-371-55170693/55170694
Address:Zhengzhou International Trade New Territory,Jinshui District,Zhengzhou ,China
Jingzhou TianHe Sci&Tech Chemical Co., Ltd.
Contact:86-716-8331612
Address:Jiangjin Road, #18, High-grade technology industries development district, Jingzhou city, Hubei province
Xinjiang Zhongtai Chemical Co., Ltd.
Contact:+86-991-8788172
Address:NO.78 XISHAN RD.URUMQI,CHINA
Contact:+86-0760-85282375
Address:zhongjing road,zhongshan torch hi-tech industrial development zone
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)