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三叶苦树叶片中新的 19(10→9)abeo-桉烷型三萜及其对一氧化氮生成的抑制活性。

New 19(10 → 9)abeo-euphane-type triterpenoids from Trichilia dregeana leaves and NO production inhibitory activities.

机构信息

Natural Products Chemistry Research Unit, Department of Chemistry, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon.

Institute of Natural Medicine, University of Toyama, 2630-Sugitani, Toyama 930-0194, Japan.

出版信息

Fitoterapia. 2024 Jul;176:106001. doi: 10.1016/j.fitote.2024.106001. Epub 2024 May 8.

Abstract

Phytochemical investigation of the EtOAc soluble fraction from leaves of Trichilia dregeana Sond. (Meliaceae) afforded naturally rare four new pentacyclic triterpenoids (1-4), together with five known pentacyclic analogs (5-8, and 11) and two steroids (9 and 10). Their structures were elucidated by extensive spectroscopic techniques such as 1D and 2D NMR and HRESIMS data analyses. The absolute configuration of 1 was determined by using the single-crystal X-ray diffraction analysis. The nitric oxide (NO) production inhibitory assay indicated that the EtOAc fraction as well as 4 and 7 inhibited the NO production in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophage cells with the IC values of 83.53 μg/mL and 81.31 and 85.71 μM, respectively. Compounds 1-4 are rare 19(10 → 9)abeo-euphane-type triterpenoids bearing a 3,10-ether bridge. To the best of our knowledge, this study is the first isolation of triterpenoids with the 3,10-ether bridge in their skeleton from the genus Trichilia, providing new insights into the chemodiversity of the terpenoids in T. dregeana.

摘要

从 Trichilia dregeana Sond.(楝科)叶的 EtOAc 可溶部分进行植物化学研究,得到了四种新的天然罕见五环三萜(1-4),以及五种已知的五环类似物(5-8 和 11)和两种甾体(9 和 10)。通过广泛的光谱技术,如 1D 和 2D NMR 和 HRESIMS 数据分析,阐明了它们的结构。通过单晶 X 射线衍射分析确定了 1 的绝对构型。一氧化氮(NO)产生抑制测定表明,EtOAc 部分以及 4 和 7 抑制脂多糖(LPS)刺激的 RAW264.7 巨噬细胞中 NO 的产生,IC 值分别为 83.53μg/mL 和 81.31 和 85.71μM。化合物 1-4 是罕见的 19(10 → 9)abeo-齐墩果烷型三萜,具有 3,10-醚桥。据我们所知,这项研究是首次从 Trichilia 属中分离出具有其骨架中 3,10-醚桥的三萜类化合物,为 T. dregeana 中萜类化合物的化学多样性提供了新的见解。

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