Li-Hong Yan , Hao-Wei Chen , Peng Hu , Jiyang Li , Juan Xiong , Ze-Xin Jin , Jin-Feng Hu
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Diaporolide, a new 10-membered lactone derivative from the endophytic Diaporthe sp. RYF-Br-5 associated with the rare conifer Keteleeria pubescens
A new 10-membered lactone derivative (diaporolide, 1) and three known polyketides (2–4) were obtained from the endophytic fungus Diaporthe sp. RYF-Br-5, which was derived from the fresh branches of Keteleeria pubescens, a rare endemic conifer native to China. Through a detailed spectroscopic analysis and theoretical ECD calculations, the structure and absolute stereochemistry of compound 1 were confirmed. In antimicrobial assays, compound 1 exhibited an inhibitory effect against Staphylococcus aureus with an MIC value of 64 µg/mL.
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.