Yizhou Bian , Sulu Qin , Shan Ran , Tao Zhu , Haiyan Fu , Wenjing Wang , Xiaolong Yang
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引用次数: 0
Abstract
Chemical investigation of the endophytic fungus Chaetomium globosum yielded two undescribed compounds: biscognin C (1), identified as a methyl-migrated analogue of biscognin B, and a rare ethyl-substituted dihydropyran derivative (2), together with seven known compounds (3−9). Their structures were unambiguously established through NMR, UV, HRESIMS, and ECD analysis. Compound 1 represents the first reported methyl-migrated biscognin analog, while compound 2 possesses an ethyl substitution distinct from dihydrodehydroacetic acid. Notably, the known compound 3 exhibited potent cytotoxicity against triple-negative breast cancer cells (MDA-MB-231) with an IC50 value of 1.64 μM. These findings expand the structural diversity of fungal secondary metabolites and highlight their potential as anticancer agents.
期刊介绍:
Phytochemistry Letters invites rapid communications on all aspects of natural product research including:
• Structural elucidation of natural products
• Analytical evaluation of herbal medicines
• Clinical efficacy, safety and pharmacovigilance of herbal medicines
• Natural product biosynthesis
• Natural product synthesis and chemical modification
• Natural product metabolism
• Chemical ecology
• Biotechnology
• Bioassay-guided isolation
• Pharmacognosy
• Pharmacology of natural products
• Metabolomics
• Ethnobotany and traditional usage
• Genetics of natural products
Manuscripts that detail the isolation of just one new compound are not substantial enough to be sent out of review and are out of scope. Furthermore, where pharmacology has been performed on one new compound to increase the amount of novel data, the pharmacology must be substantial and/or related to the medicinal use of the producing organism.