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从 中分离得到的冬凌草二萜类化合物及其抗炎和 -糖苷酶抑制活性。

Cassane diterpenoids from and their anti-inflammatory and -glycosidase inhibitory activities.

机构信息

Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry and Pharmacy, Northwest A&F University, Yangling, P. R. China.

College of Pharmacy, Chungnam National University, Daejeon, South Korea.

出版信息

Nat Prod Res. 2022 Sep;36(18):4636-4644. doi: 10.1080/14786419.2021.2007096. Epub 2021 Nov 28.

Abstract

Three undescribed cassane-type diterpenoids (CAs), caesalpulcherrins K-M (-), together with three known ones (-) were isolated from the aerial parts of (L.) Sw (Fabaceae). Their structures were elucidated via analysis of NMR (1 D and 2 D) and HRESIMS data. The character for caesalpulcherrin K possessing the olefin bond at C-11 and C-12 in its cassane skeleton was observed, which belonged to a small group among more than 450 CAs. That is, only fifteen derivatives have been reported up to now, to our knowledge. Biological evaluation revealed that compounds - exhibited moderate anti-inflammatory activity, with an IC value from 6.04 ± 0.34 to 8.92 ± 0.65 μM. Furthermore, compounds and exhibited significant -glucosidase inhibitory activity at 10 μM.

摘要

从 (L.) Sw(豆科)的地上部分分离得到三个未描述的贝壳杉型二萜(CA),caesalpulcherrin K-M(-),以及三个已知的(-)。通过分析 NMR(1D 和 2D)和 HRESIMS 数据阐明了它们的结构。观察到 caesalpulcherrin K 具有在其贝壳杉骨架中的 C-11 和 C-12 处的双键的特征,这属于在超过 450 个 CA 中的一小类。据我们所知,到目前为止,仅报道了十五个衍生物。生物评估表明,化合物-表现出中等的抗炎活性,IC 值为 6.04 ± 0.34 至 8.92 ± 0.65 μM。此外,化合物和在 10 μM 时表现出显著的 -葡萄糖苷酶抑制活性。

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