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ent-Herqueidiketal and epi-Peniciherqueinone Isolated from a Mushroom Derived Fungus Penicillium herquei YNJ-35
Authors:Hong-Yu Tan  Dr. Yu Yang  Dr. Rui Xu  Xue Zhao  Dr. Shuai-Ming Zhu  He-Xiang Gong  Zi-Lin Wang  Yue Lu  Prof. Hong-Wei Liu  Dr. Chang-Wei Li
Affiliation:1. School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, 110016 Shenyang, China

State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, 100850 Beijing, China;2. State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, 100850 Beijing, China;3. School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, 110016 Shenyang, China

Abstract:A new polyaromatic metabolite, ent-herqueidiketal ( 1 ), and a new phenalenone derivative, epi-peniciherqueinone ( 2 ), along with twelve known compounds 3 – 14 , were isolated from the fungus Penicillium herquei YNJ-35, a symbiotic fungus of Pulveroboletus brunneopunctatus collected from Nangunhe Nature Reserve, Yunnan Province, China. The structures of 1 – 14 and the absolute configurations of 1 and 2 were determined by their spectroscopic data or by their single-crystal X-ray diffraction analysis or optical rotation values. Compound 1 showed strong antibacterial activity against Staphylococcus aureus (ATCC 29213) with minimum inhibitory concentration (MIC) of 8 μg/mL. In the cytotoxicity assays, compound 1 showed weak inhibitory activity against breast cancer MCF-7 and mice microglial BV2 cells with half maximal inhibitory concentration (IC50) of 17.58 and 29.56 μM; compound 14 showed stronger cytotoxicity against BV2 and MCF-7 cells with IC50 values of 6.57 and 10.26 μM.
Keywords:antibacterial activity  cytotoxicity  Penicillium herquei  phenalenone  symbiotic fungus
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