Synthesis of optically Active 5-(3-tert-Butylamino-2-hydroxypropoxy)-3, 4-dihydrocarbostyril Hydrochloride and Their β-Adrenergic Blocking Activities
Open Access
- 1 January 1976
- journal article
- research article
- Published by Pharmaceutical Society of Japan in YAKUGAKU ZASSHI
- Vol. 96 (3), 289-292
- https://doi.org/10.1248/yakushi1947.96.3_289
Abstract
Optical isomers of 5-(3-tert-butylamino-2-hydroxypropoxy)-3,4-dihydrocarbostyril hydrochloride were synthesized and their anti-isoproterenol activity was examined in anesthetized dog. (S)(-)-isomers was about 20 times more active than (R)(+)-isomer.This publication has 4 references indexed in Scilit:
- Derivatives of 3,4-dihydrocarbostyril as .beta.-adrenergic blocking agentsJournal of Medicinal Chemistry, 1974
- STERIC ASPECTS OF ADRENERGIC DRUGS .8. OPTICAL ISOMERS OF BETA ADRENERGIC RECEPTOR ANTAGONISTS1968
- Inotropie and Chronotropic Effects of a Series of -Adrenergic Blocking Drugs: Some Structure-Activity Relationships.Experimental Biology and Medicine, 1966
- PHARMACOLOGICAL AND TOXICOLOGICAL PROPERTIES OF 2 NEW BETA-ADRENERGIC RECEPTOR ANTAGONISTS1965