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ent-Herqueidiketal and epi-Peniciherqueinone Isolated from a Mushroom Derived Fungus Penicillium herquei YNJ-35.
Tan, Hong-Yu; Yang, Yu; Xu, Rui; Zhao, Xue; Zhu, Shuai-Ming; Gong, He-Xiang; Wang, Zi-Lin; Lu, Yue; Liu, Hong-Wei; Li, Chang-Wei.
Afiliação
  • Tan HY; School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, 110016, Shenyang, China.
  • Yang Y; State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, 100850, Beijing, China.
  • Xu R; State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, 100850, Beijing, China.
  • Zhao X; State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, 100850, Beijing, China.
  • Zhu SM; State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, 100850, Beijing, China.
  • Gong HX; State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, 100850, Beijing, China.
  • Wang ZL; School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, 110016, Shenyang, China.
  • Lu Y; State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, 100850, Beijing, China.
  • Liu HW; School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, 110016, Shenyang, China.
  • Li CW; State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, 100850, Beijing, China.
Chem Biodivers ; 20(9): e202300991, 2023 Sep.
Article em En | MEDLINE | ID: mdl-37580280
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Penicillium / Agaricales Limite: Animals País como assunto: Asia Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Penicillium / Agaricales Limite: Animals País como assunto: Asia Idioma: En Ano de publicação: 2023 Tipo de documento: Article