塔芳酮A的苯二烯酮和聚酯及其结构修正

IF 3.6 2区 生物学 Q2 CHEMISTRY, MEDICINAL
Nirmal K. Chaudhary, Daniel Vuong, Ernest Lacey, Andrew M. Piggott and Peter Karuso*, 
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引用次数: 0

摘要

对丝状真菌Talaromyces stipitatus的次级代谢产物进行了研究,分离出两种新的苯烯酮二聚体talarohemiketal A(1)和talaroazasone A(2),一种新的大环内酯类聚酯talaromacrolactone A(3),以及已报道的氧苯烯酮二聚体talaromycesone A(4)、bacillisporin A(5)、bacillisporin B(6)、bacillisporin C(7)、epi-bacillisporin F(8)和bacillisporin J(9),以及苯烯酮单体funalenone(10)。15G256α(11)、15G256ν(12)和6-羟基mellein(13)。二维核磁共振相关性的详细分析,在TDDFT计算的支持下,导致了先前报道的结构14的结构修正为4。此外,对化合物8的核磁共振谱进行了校正。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Phenalenones and Polyesters from Talaromyces stipitatus and Structure Revision of Talaromycesone A

Phenalenones and Polyesters from Talaromyces stipitatus and Structure Revision of Talaromycesone A

Investigation of the secondary metabolites of the filamentous fungus Talaromyces stipitatus led to the isolation of two new phenalenone dimers, talarohemiketal A (1) and talaroazasone A (2), and one new macrolide polyester, talaromacrolactone A (3), along with the reported oxyphenalenone dimers talaromycesone A (4), bacillisporin A (5), bacillisporin B (6), bacillisporin C (7), epi-bacillisporin F (8), and bacillisporin J (9), the phenalenone monomer funalenone (10), the polyesters 15G256α (11) and 15G256ν (12), and 6-hydroxymellein (13). Detailed analysis of 2D NMR correlations, supported by TDDFT calculations, led to the structural revision of talaromycesone A as 4 from previously reported structure 14. In addition, the previously misassigned NMR spectra of compound 8 have been corrected.

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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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