| Literature DB >> 34427432 |
Chun-Xiao Jiang1,2, Bo Yu1, Ya-Mei Miao1, Hao Ren1, Qianhe Xu1, Chun Zhao1,3, Li-Li Tian1, Zhen-Qing Yu1, Pan-Pan Zhou1, Xiaolei Wang1, Jianguo Fang1, Jiwen Zhang3, Jin Z Zhang4, Quan-Xiang Wu1.
Abstract
Clonorosins A (1) and B (2), two novel indole alkaloids featuring unprecedented 6/5/6/6/5 and 6/5/5 cores, together with seven known indole-linked 2,5-diketopiperazine alkaloids (3-9), were isolated from the soil-derived fungus Clonostachys rosea YRS-06. The new structures were proposed through HR-MS, NMR, and ECD spectroscopic data. They were established by comparing the calculated NMR, ECD, and specific rotation data with the experimental. To assist in determining the absolute configuration of the chiral carbon in the side chain of 2,5-diketopiperazine derivatives, flexible analogues 3i-3iv were synthesized and analyzed. 1 was active against Fusarium oxysporum with an MIC value of 50 μg/mL. 7 and 8 showed excellent activity against human HeLa and HepG2 cells with IC50 values of 0.12-0.60 μM.Entities:
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Year: 2021 PMID: 34427432 DOI: 10.1021/acs.jnatprod.1c00457
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.803