Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10847734 | Steroids | 2010 | 5 Pages |
Abstract
A series of digoxin derivatives containing the γ-alkylidene butenolide moiety were synthesised by way of stereoselective vinylogous aldol reaction of the unactivated butenolide in simple conditions. The structures of compounds synthesised were characterised by infrared (IR), nuclear magnetic resonance (NMR) and HR-MS. Preliminary bioassay shows that some of them have cardiac functions, especially compound 2g that induced a marked increase in myocardial contractility at 10 ng mlâ1 and 20 ng mlâ1 concentrations without digitalis toxicity.
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Authors
Hai-Wei Xu, Gai-Zhi Liu, Song-Lin Zhu, Guang-Feng Hong, Hong-Min Liu, Qiong Wu,