真菌
立体化学
生物
植物
拉伤
生物碱
化学
解剖
作者
Jiajin Wu,Wenxue Wang,Yuhuan Yang,Mudassir Shah,Jixing Peng,Luning Zhou,Guojian Zhang,Qian Che,Jing Li,Tianjiao Zhu,Dehai Li,Jiajin Wu,Wenxue Wang,Yuhuan Yang,Mudassir Shah,Jixing Peng,Luning Zhou,Guojian Zhang,Qian Che,Jing Li
标识
DOI:10.1021/acs.jnatprod.4c00132
摘要
Alkaloids with a phenylhydrazone architecture are rarely found in nature. Four unusual phenylhydrazone alkaloids named talarohydrazones A-D (1-4) were isolated from the deep-sea cold seep derived fungus Talaromyces amestolkiae HDN21-0307 using the one strain-many compounds (OSMAC) approach and MS/MS-based molecular networking (MN) combined with network annotation propagation (NAP) and the unsupervised substructure annotation method MS2LDA. Their structures were elucidated by spectroscopic data analysis, single-crystal X-ray diffraction, and quantum chemical calculations. Talarohydrazone A (1) possessed an unusual skeleton combining 2,4-pyridinedione and phenylhydrazone. Talarohydrazone B (2) represents the first natural phenylhydrazone-bearing azadophilone. Bioactivity evaluation revealed that compound 1 exhibited cytotoxic activity against NCI-H446 cells with an IC50 value of 4.1 μM. In addition, compound 1 displayed weak antibacterial activity toward Staphylococcus aureus with an MIC value of 32 μg/mL.
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