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Fourteen azaphilone-type polyketides (-), including nine new ones (- and -), were isolated from cultures of -associated sp. JVF17, and their structures were determined by spectroscopic analysis together with computational methods and chemical reactions. Neuroprotective effects of the isolated compounds were evaluated against glutamate-induced neurotoxicity. Treatment with compounds , , , and - increased cell viabilities of hippocampal neuronal cells damaged by glutamate, with compound being the most potent. Compound markedly decreased intracellular Ca and nuclear condensation levels. Mechanistically, molecular markers of apoptosis induced by treatment with glutamate, i.e., phosphorylation of MAPKs and elevated Bax/Bcl-2 expression ratio, were significantly lowered by compound . The azaphilones with an isoquinoline core structure were more active than those with pyranoquinones, but -substitution decreased the activity. This study, including the structure-activity relationship, indicates that the azaphilone scaffold is a promising lead toward the development of novel neuroprotective agents.
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http://dx.doi.org/10.1021/acs.jnatprod.1c00298 | DOI Listing |
Fitoterapia
June 2025
School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China; State Key Laboratory of Pharmaceutical Biotechnology, Institute of Functional Biomolecules, Nanjing University, Nanjing 210023, China.
Two azaphilones designated as acetosellins A and B (1-2) and one new coumarin (3), along with eight other known compounds (4-11), were isolated from an endophyte Talaromyces pinophilus WRH-1 of Perilla frutescens (L.) Britt. Their structures were elucidated through detailed interpretation of UV, NMR, and HR-ESI-MS data.
View Article and Find Full Text PDFIMA Fungus
February 2025
Department of Pharmaceutical Biology, Institute of Pharmacy, Freie Universität Berlin, Königin-Luise-Str. 2+4, 14195 Berlin, Germany Freie Universität Berlin Berlin Germany.
is a plant used in Traditional Chinese Medicine. From its roots, we isolated four endophytic fungi strains. After mass spectrometry analysis and subsequent molecular networking and dereplication, one of the strain's extracts showed a cluster of yet undescribed natural products.
View Article and Find Full Text PDFJ Agric Food Chem
January 2025
Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, Yunnan Characteristic Plant Extraction Laboratory, Functional Molecules Analysis and Biotransformation Key Laboratory of Universities in Yunnan Province, School of Chemical Science and Technology, Yunnan University, K
One new azaphilone derivative () from in ordinary medium, one new phthalide derivative (), a microbial transformation product of ingredients by , a pair of new austdiol enantiomers (+)- and (-)-, one new epsilon-caprolactone derivative (), and one new ophiobolin-type sesterterpenoid () from the in host medium were reported. The structures were determined by spectroscopic analysis and single-crystal X-ray diffraction. Compounds - could completely inhibit the germination of rice seeds at 50 μg/mL, which is higher than that of the positive control.
View Article and Find Full Text PDFJ Agric Food Chem
July 2024
Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, Hunan 410013, China.
Fungal azaphilones have attracted widespread attention due to their significant potential as sources of food pigments and pharmaceuticals. Genome mining and gene cluster activation represent powerful tools and strategies for discovering novel natural products and bioactive molecules. Here, a putative azaphilone biosynthetic gene cluster from the endophytic fungus sp.
View Article and Find Full Text PDFTwo novel chlorinated and nitrogenated azaphilones, namely -butyl-2-aza-2-deoxychaetoviridin A () and -hexyl-2-aza-2-deoxychaetoviridin A (), along with a previously identified analogue, chaetoviridin A (), were successfully obtained from 2020HZ23, a marine algal-sourced endophytic fungus. The planar structures as well as the absolute configurations of these new metabolites were determined utilizing a synergistic approach that involved both spectroscopic techniques (1D/2D NMR and HRESIMS) and Density Functional Theory (DFT) calculations. Each compound was subject to cytotoxicity evaluation toward the A549 cancer cell line.
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