Journal of Medicinal Chemistry p. 1687 - 1691 (1977)
Update date:2022-08-04
Topics:
Feit
Nielsen
A number of 3,4-disubstituted 5-acylamino-, 5-alkylamino-, and 5-ureidobenzoic acids correspnding to previously described 3,4-disubstituted 5-sulfamoylbenzoic acid diuretics were prepared and screened for their diuretic properties in dogs. The tabulated results reveal that several 3,4-disubstituted 5-formamido and 5-acetamidobenzoic acids possess considerable diuretic potency demonstrating that a 5-sulfamoyl or 5-methylsulfonyl substituent is not a necessity for potent diuretic activity of 3,4-disubstituted benzoic acids. 4-Benzoyl-3-benzyloxy-5-formamidobenzoic acid, one of the most potent compounds of the present series, is approximately one-tenth as potent as bumetanide. The dose response and diuretic pattern indicate high-ceiling diuretic activity and suggest a mode of action similar to that of bumetanide.
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Doi:10.1007/BF00945287
()Doi:10.1246/cl.1986.2025
(1986)Doi:10.1021/ja00425a020
(1976)Doi:10.1016/S0039-128X(71)80143-5
(1971)Doi:10.1016/j.tetlet.2006.01.027
(2006)Doi:10.1021/jo052532+
(2006)