Suppr超能文献

来自 Godavari 红树林的 Ent-abietanes,即 Ceriops decandra:绝对构型和 NF-κB 抑制活性。

Ent-abietanes from the Godavari mangrove, Ceriops decandra: Absolute configuration and NF-κB inhibitory activity.

机构信息

Marine Drugs Research Center, College of Pharmacy, Jinan University, 601 Huangpu Avenue West, Guangzhou 510632, PR China.

School of Pharmaceutical Sciences, Southern Medical University, 1838 Guangzhou Avenue North, Guangzhou 510515, PR China.

出版信息

Fitoterapia. 2018 Oct;130:272-280. doi: 10.1016/j.fitote.2018.09.011. Epub 2018 Sep 19.

Abstract

Nine new ent-abietanes, named decandrols A-I (1-9), which could be categorized into three groups (1, 2-6, 7-9), were isolated from the roots of an Indian mangrove, Ceriops decandra, collected in the swamp of Godavari estuary, Andhra Pradesh, together with six previously reported abietanes (10-15), of which the absolute configurations were first determined. The relative and absolute configurations of these compounds were unambiguously established by HR-ESIMS, extensive 1D and 2D NMR investigations, single-crystal X-ray diffraction analysis with Cu Kα radiation, and quantum-chemical electronic circular dichroism (ECD) calculations. Decandrol A (1) is a rare C-spirofused 7,8-seco-ent-abietane, whereas 2-15 are typically tricyclic ent-abietanes. Decandrols C (3) and E (5) exhibited significant NF-κB inhibitory activity at the concentration of 100 μM.

摘要

从印度红树林植物角果木(Ceriops decandra)的根部中分离到了 9 个新的 ent-abietanes,分别命名为 decandrols A-I(1-9)(1)。这些化合物可以分为 3 组(1、2-6、7-9),同时还分离到了之前报道的 6 个 abietanes(10-15)。其中,首次确定了这些化合物的绝对构型。通过高分辨电喷雾质谱(HR-ESIMS)、广泛的 1D 和 2D NMR 研究、单晶 X 射线衍射分析(Cu Kα 辐射)和量子化学电子圆二色性(ECD)计算,明确了这些化合物的相对和绝对构型。Decandrol A(1)是一种罕见的 C-稠合 7,8-桥环 ent-abietane,而 2-15 则是典型的三环 ent-abietanes。Decandrols C(3)和 E(5)在 100 μM 的浓度下表现出显著的 NF-κB 抑制活性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验