Martel R R, Demerson C A, Humber L G, Philipp A H
J Med Chem. 1976 Mar;19(3):391-5. doi: 10.1021/jm00225a010.
A series of 37 1-ethyl- and 1-n-propyl-1, 3, 4, 9-tetrahydropyrano[3, 4-b]indole-1-acetic acids bearing one, or two, substituents on the benzene ring has been synthesized via the acid-catalyzed condensation of a substituted tryptophol with ethyl propionylacetate or ethyl butyrylacetate. Antiinflammatory and ulcerogenic effects were examined and the results show that 1, 8-diethyl-1, 3, 4, 9-tetrahydropyrano[3, 4-b]indole-1-acetic acid (etodolic acid, USAN) is a potent agent, particularly active against a chronic rat model of inflammation (ED50 0.7 + 1-0.1 mg/kg po in the adjuvant arthritis model) and which has a relatively low acute ulcerogenic potential in the same species.
通过酸催化取代色醇与丙酰乙酸乙酯或丁酰乙酸乙酯缩合,合成了一系列在苯环上带有一个或两个取代基的37种1-乙基和1-正丙基-1,3,4,9-四氢吡喃并[3,4-b]吲哚-1-乙酸。检测了其抗炎和致溃疡作用,结果表明1,8-二乙基-1,3,4,9-四氢吡喃并[3,4-b]吲哚-1-乙酸(依托度酸,美国采用名称)是一种强效药物,对慢性大鼠炎症模型尤其有效(在佐剂性关节炎模型中口服给药的半数有效量为0.7±1-0.1mg/kg),并且在同一物种中具有相对较低的急性致溃疡潜力。