Antioxidative Indole Diketopiperazine Alkaloids from Endophytic Fungi <i>Aspergillus</i> sp. JXC‐5

Three previously undescribed indole diketopiperazine alkaloids and seventeen known compounds were characterized by Aspergillus sp. JXC-5 by solid fermentation. Their structures were elucidated by spectroscopic methods and high-resolution electrospray ionization mass spectrometry, and the absolute configurations were further confirmed by electronic circular dichroism (ECD), induced CD spectra, and ML_J_DP4 methods. In the in vitro bioassays, compound 5 exhibits potent 2,2-diphenyl-1-picrylhydrazyl and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS)·+ free radicals radical scavenging activities with half-maximal inhibitory concentration values of 19.54 ± 0.39 and 26.39 ± 0.09 µM, respectively. Compounds 10-12, 14, and 15 exhibited potent ABTS·+ free radicals radical scavenging activity.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2024-12-23
DOI
https://doi.org/10.1002/cbdv.202403025
Citations
2
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.90
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Antioxidative Indole Diketopiperazine Alkaloids from Endophytic Fungi Aspergillus sp. JXC‐5

Yuchen Ma, Yin‐He Yang, Huai Xiao, Lei Huang et al.
2 citations
Chemistry & Biodiversity
Microbial Natural Products and Biosynthesis
0.90
article

Antioxidative Indole Diketopiperazine Alkaloids from Endophytic Fungi Aspergillus sp. JXC‐5

Yuchen Ma, Yin‐He Yang, Huai Xiao, Lei Huang, Wei Zhang, Geng Huang, Yan Shu, Qun Yu, Gui-Ling He
article en
2 citations

Abstract

Three previously undescribed indole diketopiperazine alkaloids and seventeen known compounds were characterized by Aspergillus sp. JXC-5 by solid fermentation. Their structures were elucidated by spectroscopic methods and high-resolution electrospray ionization mass spectrometry, and the absolute configurations were further confirmed by electronic circular dichroism (ECD), induced CD spectra, and ML_J_DP4 methods. In the in vitro bioassays, compound 5 exhibits potent 2,2-diphenyl-1-picrylhydrazyl and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS)·+ free radicals radical scavenging activities with half-maximal inhibitory concentration values of 19.54 ± 0.39 and 26.39 ± 0.09 µM, respectively. Compounds 10-12, 14, and 15 exhibited potent ABTS·+ free radicals radical scavenging activity.

Chemistry & BiodiversityVol. 22(5)
Yunnan University (CN), Dali University (CN)
Openalex Percentile: Top 22%
Microbial Natural Products and Biosynthesis
0.90
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