Bioactive Polyketides and Benzene Derivatives from Two Mangrove Sediment-Derived Fungi in the Beibu Gulf.
Bo PengJian CaiZimin XiaoManli LiuXinlong LiBin YangWei FangYi-You HuangChunmei ChenXue-Feng ZhouHuangming TaoPublished in: Marine drugs (2023)
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.
Keyphrases
- magnetic resonance
- structure activity relationship
- molecular docking
- heavy metals
- high resolution
- mass spectrometry
- escherichia coli
- molecular dynamics simulations
- signaling pathway
- high throughput
- high intensity
- candida albicans
- molecular dynamics
- ionic liquid
- computed tomography
- single cell
- risk assessment
- contrast enhanced
- small molecule
- climate change
- protein protein
- organic matter
- solid state