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New meroterpenoids and polyketides from the endophytic fungus Paraphaeosphaeria sp. C-XB-J-1 and their anti-inflammatory and SARS-CoV-2 Mpro inhibitory activities.
Li, Qi; Yang, Peng-Yun; Peng, Chao; Zhang, Xing-Jie; Jiang, Yun-Tao; Li, Yan-Ping; Gao, Lu.
Afiliación
  • Li Q; Key Laboratory of Chemistry in Ethnic Medicinal Resources of Ministry of Education, Yunnan Minzu University, Kunming 650031, Yunnan, PR China.
  • Yang PY; Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, Yunnan Characteristic Plant Extraction Laboratory, Yunnan Key Laboratory of Research and Development for Natural Products, State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, School of Ph
  • Peng C; Key Laboratory of Chemistry in Ethnic Medicinal Resources of Ministry of Education, Yunnan Minzu University, Kunming 650031, Yunnan, PR China.
  • Zhang XJ; Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, Yunnan Characteristic Plant Extraction Laboratory, Yunnan Key Laboratory of Research and Development for Natural Products, State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, School of Ph
  • Jiang YT; Key Laboratory of Chemistry in Ethnic Medicinal Resources of Ministry of Education, Yunnan Minzu University, Kunming 650031, Yunnan, PR China. Electronic address: ymujyt_2018@163.com.
  • Li YP; School of Chinese Materia Medica, Yunnan University of Chinese Medicine, Kunming 650500, Yunnan, PR China. Electronic address: lyp8691@163.com.
  • Gao L; Key Laboratory of Chemistry in Ethnic Medicinal Resources of Ministry of Education, Yunnan Minzu University, Kunming 650031, Yunnan, PR China. Electronic address: gl990@foxmail.com.
Bioorg Chem ; 147: 107315, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38604017
ABSTRACT
Seven new meroterpenoids, paraphaeones A-G (1-7), and two new polyketides, paraphaeones H-I (8-9), along with eight known compounds (10-17), were isolated from the endophytic fungus Paraphaeosphaeria sp. C-XB-J-1. The structures of 1-9 were identified through the analysis of 1H, 13C, and 2D NMR spectra, assisted by HR-ESI-MS data. Compounds 1 and 7 exhibited a dose-dependent decrease in lactate dehydrogenase levels, with IC50 values of 1.78 µM and 1.54 µM, respectively. Moreover, they inhibited the secretion of IL-1ß and CASP-1, resulting in a reduction in the activity levels of NLRP3 inflammasomes. Fluorescence microscopy results indicated that compound 7 concentration-dependently attenuated cell pyroptosis. Additionally, compounds 4 and 7 showed potential inhibitory effects on the severe acute respiratory syndrome coronavirus-2 main protease (SARS-CoV-2 Mpro), with IC50 values of 10.8 ± 0.9 µM and 12.9 ± 0.7 µM, respectively.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ascomicetos / Terpenos / Policétidos / Proteasas 3C de Coronavirus / SARS-CoV-2 Límite: Animals / Humans Idioma: En Revista: Bioorg Chem Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ascomicetos / Terpenos / Policétidos / Proteasas 3C de Coronavirus / SARS-CoV-2 Límite: Animals / Humans Idioma: En Revista: Bioorg Chem Año: 2024 Tipo del documento: Article