| Literature DB >> 23747096 |
Yi Zang1, Juan Xiong, Wen-Zhu Zhai, Lei Cao, Sheng-Ping Zhang, Yu Tang, Ji Wang, Jing-Jing Su, Guo-Xun Yang, Yun Zhao, Hui Fan, Gang Xia, Chuan-Gui Wang, Jin-Feng Hu.
Abstract
Four (1-4) hitherto unknown and seven (5-11) known ergostane-type sterols were isolated from the EtOH extract of the dried fruiting bodies of the polypore macrofungus Fomes fomentarius. On the basis of spectroscopic analysis, the structures of polyhydroxylated sterols 1-4 were elucidated to be (22E,24R)-3β,5α,6β,14α-tetrahydroxyergosta-7,9(11),22-triene (fomentarol A, 1), (22E,24R)-3β,5β,6α,7α-tetrahydroxy-8α,9α-dihydroergosta-14,22-diene (fomentarol B, 2), (22E,24R)-3β,5α-dihydroxy-6β-ethoxyergosta-7,22-diene (fomentarol C, 3), and (22E,24S)-3β,25-dihydroxy-15α-O-β-D-glucopyranosylergosta-7,22-dien-6-one (fomentarol D, 4), respectively. Rings A/B and B/C are in turn cis-fused in compound 2, which is uncommon in natural ergostane-type sterols. The potential biogenetic relationship of 2 and other ergostane-type sterols isolated from F. fomentarius was briefly discussed. Moderate cytotoxic effects of the isolated sterols against a small panel of human cancer cell lines were also established.Entities:
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Year: 2013 PMID: 23747096 DOI: 10.1016/j.phytochem.2013.05.003
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072