Format

Send to

Choose Destination
J Med Chem. 1992 Jun 26;35(13):2446-51.

Synthesis and antiulcer activity of N-substituted N'-[3-[3-(piperidinomethyl)phenoxy]propyl]ureas: histamine H2-receptor antagonists with a potent mucosal protective activity.

Author information

1
Kyorin Pharmaceutical Company, Ltd., Technical Center of Organic Syntheses, Okaya-shi, Japan.

Abstract

As an aim toward developing new antiulcer agents, new N-substituted N'-[3-[3-(piperidinomethyl)phenoxy]propyl]ureas were synthesized and evaluated for histamine H2-receptor antagonistic, gastric antisecretory, and gastric mucosal protective activities. A QSAR study showed that the most favorable N-substituents were electron-donating straight-chain alkyl groups of short length such as ethyl group from the viewpoint of dual action, i.e., gastric antisecretory and mucosal protective actions. Among the ureas studied, compounds 4, 5, and 8-10 were selected as candidates for further study.

PMID:
1352351
DOI:
10.1021/jm00091a012
[Indexed for MEDLINE]

Supplemental Content

Loading ...
Support Center