Ono S, Yamafuji T, Chaki H, Morita H, Todo Y, Okada N, Maekawa M, Kitamura K, Tai M, Narita H
Research Laboratories, Toyama Chemical Co., Ltd., Japan.
Chem Pharm Bull (Tokyo). 1995 Sep;43(9):1492-6. doi: 10.1248/cpb.43.1492.
2-(2-Aminoethoxy)-1-hydroxyethyl derivatives of bicyclic arenes (naphthalene, thianaphthene, benzofuran, and indole) were prepared and screened for antiamnestic (AA) and antihypoxic (AH) activities which were evaluated by measuring the reversing potency in electroconvulsion-induced amnesia and the protective effect against hypoxia, respectively, in mice. Compound 3o, 1-(benzo[b]thiophen-5-yl)-2- (2-diethylaminoethoxy)ethanol, showed the best AA and AH activity profile, being superior to our prototype compound, 2-(2-dimethylaminoethoxy)-1-phenylethanol (1). Elongation of the ethylene linkage in the side chain of 3o to 3- and 4-carbon moieties brought about a significant decrease in AH activity. Compound 3o was further investigated for its protective effect against CO2-induced memory impairment and for acute toxicity in mice. It is ten-fold more potent than tacrine in the amnesia-reversal assay and is considerably less toxic than tacrine.
制备了双环芳烃(萘、噻吩、苯并呋喃和吲哚)的2-(2-氨基乙氧基)-1-羟乙基衍生物,并对其抗遗忘(AA)和抗缺氧(AH)活性进行了筛选,分别通过测量小鼠电惊厥诱导遗忘中的逆转效力和对缺氧的保护作用来评估这些活性。化合物3o,1-(苯并[b]噻吩-5-基)-2-(2-二乙氨基乙氧基)乙醇,表现出最佳的AA和AH活性谱,优于我们的原型化合物2-(2-二甲氨基乙氧基)-1-苯乙醇(1)。将3o侧链中的乙烯键延长至3碳和4碳部分导致AH活性显著降低。进一步研究了化合物3o对二氧化碳诱导的记忆损伤的保护作用以及对小鼠的急性毒性。在遗忘逆转试验中,它的效力比他克林强十倍,且毒性比他克林小得多。