红树林
立体化学
聚酮
化学
细胞毒性
生物信息学
药效团
二维核磁共振波谱
圆二色性
酶
生物
生物化学
生物合成
体外
生态学
基因
作者
Bo Peng,Jian Cai,Zimin Xiao,Manli Liu,Xinlong Li,Bin Yang,Wei Fang,Yi‐You Huang,Chunmei Chen,Xuefeng Zhou,Huaming Tao
出处
期刊:Marine Drugs
[MDPI AG]
日期:2023-05-26
卷期号:21 (6): 327-327
被引量:6
摘要
To discover bioactive natural products from mangrove sediment-derived microbes, a chemical investigation of the two Beibu Gulf-derived fungi strains, Talaromyces sp. SCSIO 41050 and Penicillium sp. SCSIO 41411, led to the isolation of 23 natural products. Five of them were identified as new ones, including two polyketide derivatives with unusual acid anhydride moieties named cordyanhydride A ethyl ester (1) and maleicanhydridane (4), and three hydroxyphenylacetic acid derivatives named stachylines H-J (10-12). Their structures were determined by detailed nuclear magnetic resonance (NMR) and mass spectroscopic (MS) analyses, while the absolute configurations were established by theoretical electronic circular dichroism (ECD) calculation. A variety of bioactive screens revealed three polyketide derivatives (1-3) with obvious antifungal activities, and 4 displayed moderate cytotoxicity against cell lines A549 and WPMY-1. Compounds 1 and 6 at 10 μM exhibited obvious inhibition against phosphodiesterase 4 (PDE4) with inhibitory ratios of 49.7% and 39.6%, respectively, while 5, 10, and 11 showed the potential of inhibiting acetylcholinesterase (AChE) by an enzyme activity test, as well as in silico docking analysis.
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