| Literature DB >> 28228227 |
Patima Phainuphong1, Vatcharin Rukachaisirikul2, Kwanruthai Tadpetch1, Yaowapa Sukpondma1, Saowanit Saithong1, Souwalak Phongpaichit3, Sita Preedanon4, Jariya Sakayaroj4.
Abstract
Chromatographic separation of the broth extract of the soil-derived fungus Aspergillus sclerotiorum PSU-RSPG178 resulted in isolation of four γ-butenolide-furanone dimers, aspersclerotiorones A-D, a furanone derivative, aspersclerotiorone E, and two γ-butenolide derivatives, aspersclerotiorones F and G, together with six known compounds, penicillic acid, dihydropenicillic acid, 5,6-dihydro-6-hydroxypenicillic acid, 6-methoxy-5,6-dihydropenicillic acid, coculnol and (4R,5R)-4,5-dihydroxy-3-methoxy-5-methylcyclohex-2-en-1-one. Their structures were determined by spectroscopic evidence. For aspersclerotiorones A and B, the structures were confirmed by single-crystal X-ray diffraction crystallography. Penicillic acid displayed weak antibacterial activity against Staphylococcus aureus and Escherichia coli with equal MIC values of 128 μg/mL, and it was noncytotoxic towards African green monkey kidney fibroblast cells.Entities:
Keywords: Antibacterial; Antifungal; Aspergillus sclerotiorum; Cytotoxic; Furanone derivatives; γ-butenolides
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Year: 2017 PMID: 28228227 DOI: 10.1016/j.phytochem.2017.02.008
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072