Acylated triterpenoid saponins from the stem bark of Foetidia africana.

Acylated triterpenoid saponins from the stem bark of Foetidia africana.
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来自非洲 Foetidia africana 茎皮的酰化三萜皂苷。

DOI:
10.1021/np020151a
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发表时间:
2002
影响因子:
5.1
通讯作者:
C. Lavaud
C. Lavaud
中科院分区:
生物学2区
文献类型:
--
作者:
Marie;Isabelle Pouny;C. Delaude;C. Lavaud

文献摘要

被引文献

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从非洲 Foetidia africana 的茎皮中分离得到 9 个新的酰化三萜皂苷 (4-12)。它们都具有作为糖苷配基的barringtogenol C,被乙酸和/或异戊酸酯化。糖链最多由三个单元组成:D-葡萄糖醛酸 (GlcUA) 连接到糖苷配基的 C-3,并被 D-半乳糖 (Gal)(在 GlcUA C-2 处)和/或 L-鼠李糖 (Rha)(在 GlcUA C-4 处)取代。通过酸和碱水解、NMR 实验(包括 (1)H-(1)H (COSY、HOHAHA、ROESY) 和 (1)H-(13)C (HSQC、HMBC) 光谱)以及质谱 (ESIMS、ESIMS(n)) 确定结构。
Nine new acylated triterpenoid saponins (4-12) were isolated from the stem bark of Foetidia africana. They all possess barringtogenol C as the aglycone, esterified by acetic and/or isovaleric acids. The sugar chain consists of up to three units: D-glucuronic acid (GlcUA) linked to C-3 of the aglycone and substituted by D-galactose (Gal) (at GlcUA C-2) and/or L-rhamnose (Rha) (at GlcUA C-4). The structures were established by acid and alkaline hydrolysis, by NMR experiments including (1)H-(1)H (COSY, HOHAHA, ROESY) and (1)H-(13)C (HSQC, HMBC) spectroscopy, and by mass spectrometry (ESIMS, ESIMS(n)).