Adpressins A-G: Oligophenalenone Dimers from Talaromyces adpressus.

IF 3.3 2区 生物学 Q2 CHEMISTRY, MEDICINAL Journal of Natural Products Pub Date : 2024-08-23 Epub Date: 2024-07-21 DOI:10.1021/acs.jnatprod.4c00330
Meijia Zheng, Qin Li, Hong Liao, Yongqi Li, Chenxi Zhou, Xinyi Zhao, Chunmei Chen, Weiguang Sun, Yonghui Zhang, Hucheng Zhu
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引用次数: 0

摘要

从真菌 Talaromyces adpressus 中分离出了九种新的低聚苯丙酮二聚体 adpressins A-G(1-9)和九种已知化合物(10-18)。根据光谱和质谱分析确定了它们的化学结构。通过 1H 和 13C NMR 计算、DP4+ 分析、电子圆二色性(ECD)计算以及 ECD 光谱与相关化合物的比较,确定了它们的相对和绝对构型。化合物 1 是首个具有不寻常的 6/6/6/5/6/6 环系统的杜仲苷衍生物,而化合物 6 和 7 则含有一个新颖的吡咯烷环。化合物 5、9 和 18 对 LPS 诱导的 B 淋巴细胞增殖有中度抑制作用,IC50 值在 1.6 到 8.6 μM 之间。此外,化合物 9 和 18 对 Con A 诱导的 T 淋巴细胞增殖也有中度抑制作用,IC50 值分别为 9.3 和 2.6 μM。
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Adpressins A-G: Oligophenalenone Dimers from Talaromyces adpressus.

Nine new oligophenalenone dimers, adpressins A-G (1-9), together with nine known compounds (10-18), were isolated from the fungus Talaromyces adpressus. Their chemical structures were determined on the basis of spectroscopic and mass spectral analyses. Their relative and absolute configurations were identified by 1H and 13C NMR calculations followed by DP4+ analyses, electronic circular dichroism (ECD) calculations, and ECD spectra comparison with related compounds. Compound 1 is the first example of a duclauxin derivative featuring an unusual 6/6/6/5/6/6/6 ring system, while compounds 6 and 7 contained a novel pyrrolidine ring. Compounds 5, 9, and 18 exhibited moderate inhibition against LPS-induced B lymphocyte proliferation with IC50 values ranging from 1.6 to 8.6 μM. Additionally, compounds 9 and 18 exhibited moderate inhibition against Con A-induced T lymphocyte proliferation with IC50 values of 9.3 and 2.6 μM, respectively.

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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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