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.
v. Braun; Braunsdorf, Chemische Berichte, 1921, vol. 54, p. 2084
作者:v. Braun、Braunsdorf
DOI:——
日期:——
FRIES D. S.; ANDRAKO J.; HUDGINS P., J. MED. CHEM. <JMCM-AR>, 1977, 20, NO 10, 1250-1254