Angiotensin converting enzyme inhibitors: 1, 5-benzothiazepine derivatives
J Slade, JL Stanton, D Ben-David…
Index: Slade; Stanton; Ben-David; Mazzenga Journal of Medicinal Chemistry, 1985 , vol. 28, # 10 p. 1517 - 1521
Full Text: HTML
Citation Number: 73
Abstract
The synthesis of chiral 1, 5-benzothiazepines 2a-c, 14a-q 15c, and 16a prepared from cysteine is described. In vitro inhibition of angiotensin converting enzyme (ACE) is reported for each compound. Compound 2c was the most potent in vitro having an ICm of 2.95 nM. The ester of 2c, ie 14c, was found to inhibit the AI pressor response by 75% at a dose of 0.05 mg/kg iv and by 39% at 1.0 mg/kg PO. Additionally, 14c lowered blood pressure in the ...
Related Articles:
Detoxification Metabolism of o-Dinitrobenzene by the Yeast Issatchenkia orientalis
[Tamaki, Hisanori; Kumagai, Hidehiko; Shimada, Yoshimi; Kashima, Takanori; Obata, Hiroshi; et al Agricultural and Biological Chemistry, 1991 , vol. 55, # 4 p. 951 - 956]