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Pleosmaranes A-R、异松烷和 20-降异松烷二萜类化合物具有抗炎活性,来自红树林内生真菌 sp. HNQQJ-1。

Pleosmaranes A-R, Isopimarane and 20-nor Isopimarane Diterpenoids with Anti-inflammatory Activities from the Mangrove Endophytic Fungus sp. HNQQJ-1.

机构信息

School of Pharmacy, Anhui Medical University, Hefei 230032, China.

National R & D Center for Edible Fungus Processing Technology, Henan University, Kaifeng 475004, China.

出版信息

J Nat Prod. 2024 Feb 23;87(2):304-314. doi: 10.1021/acs.jnatprod.3c00893. Epub 2024 Feb 6.

Abstract

Pleosmaranes A-R (-), 18 new isopimarane-type diterpenoids, together with four known analogs (-), were isolated from the mangrove endophytic fungus sp. HNQQJ-1. Their structures and absolute configurations were established by analysis of their spectroscopic data and electronic circular dichroism (ECD) calculations. Compounds - possess an unusual aromatic B ring and a 20-nor-isopimarane skeleton. Compounds - contain a unique 2-oxabicyclo[2.2.2]octane moiety. Compound features an unexpected 2-oxabicyclo[3.2.1]octane moiety. Compounds and exhibited a moderate inhibitory effect against LPS-induced NO production, with IC values of 19 and 25 μM, respectively.

摘要

Pleosmaranes A-R(-),18 种新的异松烷型二萜类化合物,以及四种已知类似物(-),从红树林内生真菌 sp. HNQQJ-1 中分离得到。通过分析其光谱数据和电子圆二色性(ECD)计算,确定了它们的结构和绝对构型。化合物-具有不寻常的芳香 B 环和 20-降异松烷骨架。化合物-含有独特的 2-氧杂双环[2.2.2]辛烷部分。化合物-具有出乎意料的 2-氧杂双环[3.2.1]辛烷部分。化合物-和-对 LPS 诱导的 NO 产生具有中等抑制作用,IC 值分别为 19 和 25 μM。

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