Structure elucidation and conformational properties of eprosartan a non peptide Angiotensin II AT1 antagonist

被引:25
|
作者
Zoumpoulakis, P
Grdadolnik, SG
Matsoukas, J
Mavromoustakos, T
机构
[1] Natl Hellen Res Fdn, Inst Organ & Pharmaceut Chem, Athens 11635, Greece
[2] Natl Inst Chem, SI-1115 Ljubljana, Slovenia
[3] Univ Patras, Dept Chem, Patras 26500, Greece
关键词
antihypertensives; eprosartan; losartan; AT; antagonists; NMR; molecular modeling;
D O I
10.1016/S0731-7085(01)00603-3
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel approach to treat hypertension is to interfere with the Renin-Angiotensin system (RAS) by blocking the binding of vasoconstrictive hormone Angiotensin II to the AT, receptor site. This approach led to the beneficial drug losartan (COZAAR) and other similar in structure to the antihypertensive drugs (sartans). In an effort to compare the stereoelectronic features of pharmacophoric segments of the different sartans, a research activity was initiated in our laboratory related to the conformational properties of these drugs. In a previous study, the structural features which determine the pharmacophoric segments of losartan were examined. In this study, the conformational properties of eprosartan (TEVETEN), a drug with fewer side effects, were examined. In addition, the superimposition ability of losartan and eprosartan with the peptide antagonist sarmesin was studied. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:125 / 135
页数:11
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