平山青霉中的氮氮酚类色素

Colorants Pub Date : 2023-01-25 DOI:10.3390/colorants2010003
Coralie Pavesi, V. Flon, G. Genta‐Jouve, E. Pramil, A. Escargueil, Adeel Nasir, T. Montier, X. Franck, Soizic Prado
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引用次数: 1

摘要

真菌色素作为染料的使用在各个工业领域都具有吸引力。真菌色素因其不具有合成色素的缺点而适合大规模工业生产而引起人们的强烈兴趣。与合成或植物染料相比,它们的优势使它们成为首要目标。氮杂霉酮是一种真菌多酮类色素,具有高氧吡醌双环核心,由许多子囊菌和担子菌真菌产生。为了寻找新的氮唑啉类染料,我们利用分子网络技术对已知的氮唑啉类化合物平山青霉U进行了研究,并分离出了三种新的氮唑啉类化合物:penazaphilone J-L、penazaphilone D、isochromophilone VI和clerketide e。所有化合物对人类细胞系和人类病原体抗性菌株的细胞毒活性进行了评估。
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Azaphilones Pigments from the Fungus Penicillium hirayamae
The use of fungal pigments as dyes is attractive for various industries. Fungal pigments arise a strong interest because they are suitable for large-scale industrial production and have none of the drawbacks of synthetic pigments. Their advantages over synthetic or vegetal dyes mark them as a prime target. Azaphilones are fungal polyketides pigments bearing a highly oxygenated pyranoquinone bicyclic core produced by numerous species of ascomyceteous and basidiomyceteous fungi. In order to find new azaphilones dyes, the fungal strain Penicillium hirayamae U., a known producer of azaphilone but, chemically, barely studied so far, was investigated by molecular networking and led to the isolation of three new azaphilones, penazaphilone J-L, along with the known penazaphilone D, isochromophilone VI, and sclerketide E. Their structures were determined based on extensive NMR and the absolute configurations by ECD. All compounds were evaluated for their cytotoxic activity against human cell lines and human pathogenic-resistant strains.
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