2-(Aminomethyl)phenols, a new class of saluretic agents. 5. Fused-ring analogs

A number of bicyclic ring-fused analogues of 2-(aminomethyl)phenol were synthesized and tested orally in rats and intravenously in dogs for saluretic and diuretic effects. Of the 15 alicylic, aromatic, and heterocyclic ring-fused compounds tested, only 2-(aminomethyl)-4-chloro-1-naphthalenol hydroch...

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Bibliographic Details
Published in:Journal of medicinal chemistry Vol. 26; no. 4; pp. 580 - 585
Main Authors: Deana, A. A, Stokker, G. E, Schultz, E. M, Smith, R. L, Cragoe, E. J, Russo, H. F, Watson, L. S
Format: Journal Article
Language:English
Published: United States American Chemical Society 01-04-1983
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Summary:A number of bicyclic ring-fused analogues of 2-(aminomethyl)phenol were synthesized and tested orally in rats and intravenously in dogs for saluretic and diuretic effects. Of the 15 alicylic, aromatic, and heterocyclic ring-fused compounds tested, only 2-(aminomethyl)-4-chloro-1-naphthalenol hydrochloride (2) and 7-(aminomethyl)-6-hydroxy-5,8-dimethyl-1,2,3,4-tetrahydronaphthalene hydrochloride (6) displayed a high order of activity.
Bibliography:ark:/67375/TPS-QCGV5608-2
istex:1ADD8009B5544442D18A7E48679A0F1A5E6B0625
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0022-2623
1520-4804
DOI:10.1021/jm00358a023