Cytotoxic and Cell Proliferation Activities of Isocoumarin Derivatives Isolated from Phialocephala scopiformis FC-1873
- 1 School of Pharmacy and Pharmaceutical Sciences, Hoshi University, Tokyo, Japan
- 2 School of Pharmacy and Pharmaceutical Sciences, Hoshi University, Tokyo, Japan
- 3 School of Pharmacy and Pharmaceutical Sciences, Hoshi University, Tokyo, Japan
- 4 School of Pharmacy and Pharmaceutical Sciences, Hoshi University, Tokyo, Japan
- 5 School of Pharmacy and Pharmaceutical Sciences, Hoshi University, Tokyo, Japan
- 6 School of Pharmacy and Pharmaceutical Sciences, Hoshi University, Tokyo, Japan
- 7 School of Pharmacy and Pharmaceutical Sciences, Hoshi University, Tokyo, Japan
- 8 Department of Botany, National Museum of Nature and Science, Ibaraki, Japan
- 9 Department of Botany, National Museum of Nature and Science, Ibaraki, Japan
- 10 School of Pharmacy and Pharmaceutical Sciences, Hoshi University, Tokyo, Japan
- 11 Faculty of Pharmacy and Pharmaceutical Sciences, School of Pharmacy, Josai University, Saitama, Japan
- 12 Faculty of Pharmacy, Juntendo University, Chiba, Japan
- 13 River Museum of Saitama, Saitama, Japan
Abstract
Phialocephala scopiformis (Ascomycota, Helotiales, Mollisiaceae) are fungi known as both saprophytes and endophytes, forming small apothecia (1 - 3 mm in diameter) on decaying wood. In this study, three novel isocoumarin derivatives (+)-phaeosphaerin A ( 1 ), (+)-phaeosphaerin B ( 2 ), and ( S )-6-demethylkigelin ( 3 ) were isolated from Phialocephala scopiformis FC-1873 collected in Japan, along with two known isocoumarins, lignicol ( 4 ) and 6,8-dihydroxy-3,5-dimethyl-1 H -2-benzopyran-1-one ( 5 ). The cytotoxicity of 1 and 4 were evaluated against HL-60, PANK-1, HepG2, HT-29, and T98G cell lines, as well as their effects on cell proliferation in the skin keratinocyte cell line HaCaT. These findings highlight the potential of mollisioid fungi as a source of novel bioactive compounds.
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