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Chemical constituents from the fruiting bodies of Cryptoporus volvatus
Junchi Wang,Guangzhi Li,Na Lv,Li Gao,Liangang Shen,Jianyong Si 대한약학회 2016 Archives of Pharmacal Research Vol.39 No.6
New drimane-type sesquiterpene cryptoporol A(1), cryptoporic acid derivative 60-cryptoporic acid E methylester (2), and pseudouridine derivative cryptoporineA(3), aswell as a known ergosterol 5a,8a-epidioxy-22E-ergosta-6,22-dien-3b-ol (4), were isolated from a 90 % alcoholextract of the fruiting bodies of Cryptoporus volvatus. Thestructures of these compounds were established by spectroscopicanalysis and circular dichroism. 5a,8a-epidioxy-22Eergosta-6,22-dien-3b-ol (4) exhibited antiviral activityagainst porcine reproductive and respiratory syndrome virus,and all compounds showed weak antioxidant activities.
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Guangzhi Li,Junchi Wang,Xiaojin Li,Jianguo Xu,Zhao Zhang,Jianyong Si 대한약학회 2018 Archives of Pharmacal Research Vol.41 No.6
20-Z auraptene (1) is a synthesized monoterpenecoumarin with anticancer activity against human gastriccancer cells. In order to find new potential anticancer agent,Mucor polymorphosporus was used to transform cis-auraptene. Four new terpene coumarins with notable changesin the skeletal backbone, 20-Z auraptene A-D (2–5), wereobtained and evaluated for their antiproliferative effectsagainst human normal gastric epithelium cells and humangastric cancer cells. These new compounds showed selectivecytotoxic activity against MGC-803 cells with IC50values from 0.78 ± 0.13 to 10.78 ± 1.83 lM and thetherapeutic index could also be significantly improved(TI = 59.0) compared with that of 1 (TI = 5.5). Thestructures of these metabolites were elucidated throughextensive spectroscopic methods, and the possible biotransformationpathway of 1 by Mucor polymorphosporuswas also proposed. Furthermore, the mechanism of theantiproliferative effects against MGC-803 cells of the mostpotent compound, 20-Z auraptene A (2), was characterized. Annexin V/PI staining and abnormal expression of apoptosis-related protein suggested that compound 2 inducesapoptosis in gastric cancer MGC-803 cells. Therefore, it ispossible that compound 2 has the potential to be applied ingastric cancer therapy.
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