Witty T R, Remers W A, Besch H R
J Pharm Sci. 1975 Jul;64(7):1248-50. doi: 10.1002/jps.2600640731.
A series of compounds related to 3-deoxydigitoxigenin was prepared and assayed for inhibition of myocardial Na+,K+- adenosine triphosphatase. Although the relatively high activity of 3-deoxydigitoxin was confirmed, the corresponding 3beta,4beta-epoxide and a mixture of 2,3-olefins and 3,4-olefins were less active. 3-Deoxy compounds with variations at the 14-position and the butenolide ring were much less active than the corresponding 3beta-hydroxy analogs. Thus the activity of 3-deoxydigitoxigenin appears to be particularly susceptible to structural changes elsewhere in the molecule.
制备了一系列与3-脱氧洋地黄毒苷元相关的化合物,并测定了它们对心肌钠钾-三磷酸腺苷酶的抑制作用。尽管证实了3-脱氧洋地黄毒苷具有较高的活性,但相应的3β,4β-环氧化物以及2,3-烯烃和3,4-烯烃的混合物活性较低。在14位和丁烯内酯环有变化的3-脱氧化合物比相应的3β-羟基类似物活性低得多。因此,3-脱氧洋地黄毒苷元的活性似乎特别容易受到分子中其他部位结构变化的影响。