Benzylpiperazine derivatives. V. Quantitative structure-activity relationships of 1-benzyl-4-diphenylmethylpiperazine derivatives for cerebral vasodilating activity.
- 31 December 1986
- journal article
- research article
- Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN
- Vol. 35 (10) , 4117-4123
- https://doi.org/10.1248/cpb.35.4117
Abstract
The quantitative structure-activity relationships of 1-benzyl-4-diphenylmethylpiperazines for the cerebral vasodilating activity in dogs and duration of action were examined. The analyses indicate that increase of the electron density on the benzylic nitrogen atom and the intoroduction of sterically small substituents at the para position of the diphenylmethyl moiety bring about strong interactions of the molecule with the active site and result in high potency as well as prolonged action.This publication has 4 references indexed in Scilit:
- Benzylpiperazine derivatives. III. Quantitative structure - cerebral vasodilating activity relationships of 1-benzyl-4-(3-hydroxy-3-phenylpentyl)piperazine derivatives.CHEMICAL & PHARMACEUTICAL BULLETIN, 1987
- Benzylpiperazine derivatives. IV. Syntheses and cerebral vasodilating activities of 1-benzyl-4-diphenylmethylpiperazine derivatives.CHEMICAL & PHARMACEUTICAL BULLETIN, 1987
- Adaptive least-squares method applied to structure-activity correlation of hypotensive N-alkyl-N''-cyano-N'-pyridylguanidinesJournal of Medicinal Chemistry, 1979
- UNSYMMETRICALLY DISUBSTITUTED PIPERAZINES. III. N-METHYL-N'-BENZHYDRYLPIPERAZINES AS HISTAMINE ANTAGONISTS1The Journal of Organic Chemistry, 1949