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
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.