STRUCTURE-ACTIVITY STUDY OF ANTIHYPERTENSIVE 1,4-DIHYDROPYRIDINE DERIVATIVES HAVING NITROOXYALKYL MOIETIES AT THE 3 AND 5 POSITIONS

Citation
Y. Kawashima et al., STRUCTURE-ACTIVITY STUDY OF ANTIHYPERTENSIVE 1,4-DIHYDROPYRIDINE DERIVATIVES HAVING NITROOXYALKYL MOIETIES AT THE 3 AND 5 POSITIONS, Chemical and Pharmaceutical Bulletin, 41(6), 1993, pp. 1060-1065
Citations number
12
Categorie Soggetti
Pharmacology & Pharmacy",Chemistry
ISSN journal
00092363
Volume
41
Issue
6
Year of publication
1993
Pages
1060 - 1065
Database
ISI
SICI code
0009-2363(1993)41:6<1060:SSOA1D>2.0.ZU;2-U
Abstract
1,4-Dihydropyridine derivatives having two nitrooxyalkyl moieties as e sters at the 3 and 5 position possess antihypertensive activity. To un derstand how substituents affect the biological activity, the quantita tive structure-activity relationship (QSAR) of 27 compounds was analyz ed using the Fuzzy adaptive least-squares (FALS 91) method. The QSAR m odels suggested that the hydrophobicity and electronic effect at the 4 position of the 1,4-dihydropyridine along with the special structures of the nitrooxyalkylester components are important for antihypertensi ve activity.