STOKKER G. E.; DEANA A. A.; SOLMS S. J. DE; SCHULTZ E. M.; SMITH R. L.; C+, J. MED. CHEM., 1980, 23, NO 12, 1414-1427,
作者:STOKKER G. E.、 DEANA A. A.、 SOLMS S. J. DE、 SCHULTZ E. M.、 SMITH R. L.、 C+
DOI:——
日期:——
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution
作者:G. E. Stokker、A. A. Deana、S. J. DeSolms、E. M. Schultz、R. L. Smith、E. J. Cragoe、J. E. Baer、C. T. Ludden、H. F. Russo
DOI:10.1021/jm00186a024
日期:1980.12
A series of 2-(aminomethyl)phenols was synthesized and tested in rats and dogs for saluretic and diuretic activity. A number of these compounds exhibit a high order of activity on iv or po administration. The most active compounds belong to a subseries of 4-alkyl-6-halo derivatives of which 2, 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol, is the most active. Compound 2 also possesses significant