Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1374851 | Bioorganic & Medicinal Chemistry Letters | 2009 | 4 Pages |
Abstract
Cytotoxicity-guided phytochemical analysis on the extract of Lysimachia heterogenea Klatt led to the isolation of 3β,16β-12-oleanene-3,16,23,28-tetrol (1) and its four new oligosaccharidic derivatives heterogenosides A, B, C, and D (2-5). Their structural elucidation was mainly based on NMR and mass spectral data. The time course experimental results indicated that unlike the likely lysis activity of heterogenosides B-D, heterogenoside A showed a significantly time-dependent cytotoxicity.
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Chemistry
Organic Chemistry
Authors
Xin-an Huang, Yong-ju Liang, Xiao-ling Cai, Xiao-quan Feng, Chuan-hai Zhang, Li-wu Fu, Wen-di Deng,