Synthesis and preliminary pharmacological activity of aminoalkoxy isosteres of glycolate ester anticholinergics
作者:David S. Fries、John Andrako、Patricia Hudgins
DOI:10.1021/jm00220a005
日期:1977.10
A sides of 2-(N-substituted amino)alkoxy-1,1-diphenylethanols was synthesized and evaluated for anticholinergic activity. The compounds differ structurally from the glycolate ester-type anticholinergic compounds by the bioisosteric substitution of a methylene group for the ester carbonyl moiety. The ethers which result from this change have increased lipophilicity compared to their ability to inhibit perphenazine-induced catatonia in rats. Structure-activity relationships of the compounds are discussed.
FRIES D. S.; ANDRAKO J.; HUDGINS P., J. MED. CHEM. <JMCM-AR>, 1977, 20, NO 10, 1250-1254
作者:FRIES D. S.、 ANDRAKO J.、 HUDGINS P.
DOI:——
日期:——
Kusnezow; Bobyschewa, Zhurnal Obshchei Khimii, 1958, vol. 28, p. 521,524; engl. Ausg. S. 511, 513