Abstract
A series of n-butylphthalide derivatives were designed and synthesized. The in vitro activities of these compounds were evaluated by a resting tension of isolated rat thoracic aorta ring assay. Compounds 4g and 4i were found to be more active than n-butylphthalide.
Copyright (c) 2010 Elsevier Masson SAS. All rights reserved.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Aorta, Thoracic / drug effects*
-
Aorta, Thoracic / metabolism
-
Benzofurans / chemical synthesis*
-
Benzofurans / chemistry
-
Benzofurans / pharmacology*
-
Dose-Response Relationship, Drug
-
Drug Evaluation, Preclinical
-
Mice
-
Molecular Structure
-
Rats
-
Stereoisomerism
-
Vasodilator Agents / chemical synthesis*
-
Vasodilator Agents / chemistry
-
Vasodilator Agents / pharmacology*
Substances
-
Benzofurans
-
Vasodilator Agents
-
3-n-butylphthalide