来自海洋海绵 Diacarnus spinipoculum 的去甲萜环状过氧化物,瞬时受体电位 Ankyrin 1 的抑制剂。

IF 3.6 2区 生物学 Q2 CHEMISTRY, MEDICINAL
Yeonwoo Cho, Chinmayee Bawkar, Jung Mi Hyun, Myung Jin Song, Kwiwan Jeong and Yeon-Ju Lee*, 
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引用次数: 0

摘要

在生物测定的指导下,从海洋海绵 Diacarnus spinipoculum 提取物中分离出了对人类瞬时受体电位安基蛋白 1(hTRPA1)具有抑制活性的 12 种北端萜环过氧化物(1-12)和 8 种北端萜环过氧化物(13-20)。其中 10 种(5-7、11、12、16-20)是前所未有的类似物。在环己酮分子上附有羟基(5、11)或甲氧基(6、12)的化合物是在 C-11 处获得的表聚混合物,而化合物 4、6、10 和 12 很可能是分离的产物。新化合物的绝对构型是根据基于核磁共振的经验方法和比旋值比较确定的。莫舍酯分析揭示了 17-20 号化合物的绝对构型。分离出的化合物对 hTRPA1 的抑制活性因其结构的不同而有显著差异,其中后萜类化合物 19 的活性最强(IC50 2.0 μM)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Norterpene Cyclic Peroxides from the Marine Sponge Diacarnus spinipoculum, Inhibitors of Transient Receptor Potential Ankyrin 1

Norterpene Cyclic Peroxides from the Marine Sponge Diacarnus spinipoculum, Inhibitors of Transient Receptor Potential Ankyrin 1

Norterpene Cyclic Peroxides from the Marine Sponge Diacarnus spinipoculum, Inhibitors of Transient Receptor Potential Ankyrin 1

Bioassay-guided isolation of the extract from the marine sponge Diacarnus spinipoculum showing inhibitory activity against human transient receptor potential ankyrin 1 (hTRPA1) resulted in the isolation of 12 norditerpene cyclic peroxides (112) and eight norsesterterpene cyclic peroxides (1320). Among these, 10 (57, 11, 12, 1620) are unprecedented analogs. Compounds with either a hydroxy (5, 11) or a methoxy (6, 12) group attached to the cyclohexanone moiety were obtained as epimeric mixtures at C-11, while compounds 4, 6, 10, and 12 are likely the artifacts of isolation. The absolute configurations of the new compounds were established based on an NMR-based empirical method and comparison of specific rotation values. Mosher ester analysis revealed the absolute configurations of compounds 1720. The inhibitory activity of the isolated compounds against hTRPA1 varied significantly depending on their structures, with the norsesterterpenoid 19 displaying the most potent activity (IC50 2.0 μM).

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来源期刊
CiteScore
9.10
自引率
5.90%
发文量
294
审稿时长
2.3 months
期刊介绍: The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin. When new compounds are reported, manuscripts describing their biological activity are much preferred. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
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