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南海软珊瑚中具有神经保护潜力的罕见碳萨宁二萜。

Uncommon Capnosane Diterpenes with Neuroprotective Potential from South China Sea Soft Coral .

机构信息

School of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing 210023, China.

State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555, Zu Chong Zhi Road, Zhangjiang Hi-Tech Park, Shanghai 201203, China.

出版信息

Mar Drugs. 2022 Sep 25;20(10):602. doi: 10.3390/md20100602.

Abstract

The first investigation of the South China Sea soft coral afforded five new capnosane diterpenes, sarboettgerins A-E (-), together with one known related compound, pavidolide D (). Their structures, including absolute configurations, were elucidated by the extensive spectroscopic analysis, C NMR calculations, and X-ray diffraction. Among them, new compounds - were featured by the rarely encountered -geometry double bond Δ within the 5/11-fused bicyclic capnosane carbon framework. Plausible biogenetic relationships of all isolates were proposed, and they might give an insight into future biomimetic synthesis of these novel compounds. In an in vitro bioassay, compound displayed potent anti-neuroinflammatory activity against LPS-induced NO release in BV-2 microglial cells, which might be developed as a new type of potential neuroprotective agent in future.

摘要

南海软珊瑚的首次调查提供了五个新的卡普萨诺二萜,sarboettgerins A-E(-),以及一个已知的相关化合物,pavidolide D()。通过广泛的光谱分析、C NMR 计算和 X 射线衍射,确定了它们的结构,包括绝对构型。其中,新化合物 - 具有在 5/11 稠合双环卡普萨诺碳骨架内罕见的 - 几何双键 Δ。所有分离物的可能生物发生关系被提出,它们可能为这些新型化合物的未来仿生合成提供一个深入了解。在体外生物测定中,化合物显示出对 LPS 诱导的 BV-2 小胶质细胞中 NO 释放的强烈抗神经炎症活性,这可能为未来开发新型潜在神经保护剂提供了可能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8593/9604702/169be43c4e9e/marinedrugs-20-00602-g001.jpg

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