Cytotoxic Kendomycins Containing the Carbacylic Ansa Scaffold from the Marine-Derived Verrucosispora sp. SCSIO 07399.
Shanwen ZhangQing XieChangli SunXin-Peng TianChun GuiXiangjing QinHua ZhangJianhua JuPublished in: Journal of natural products (2019)
Three new kendomycin analogues, kendomycins B-D (1-3), were discovered from the marine-derived actinomycete Verrucosispora sp. SCSIO 07399. The structures of 1-3 were elucidated using diverse spectroscopic data analyses, X-ray crystallography, and semisynthetic derivatization. In vitro antimicrobial assays revealed that 1-3 all display good antibacterial activities against six Gram-positive bacteria with MIC values ranging from 0.5 to 8.0 μg/mL. Additionally, 1-3 were found to be moderately cytotoxic against MGC803, A549, HeLa, HepG2, MCF-7, and RKO human tumor cell lines; IC50 values ranged from 2.2 to 44 μM.
Keyphrases
- molecular docking
- high resolution
- endothelial cells
- staphylococcus aureus
- ms ms
- electronic health record
- high throughput
- single cell
- big data
- high performance liquid chromatography
- induced pluripotent stem cells
- simultaneous determination
- pluripotent stem cells
- computed tomography
- machine learning
- magnetic resonance imaging
- magnetic resonance
- cell death
- anti inflammatory
- gas chromatography
- signaling pathway
- cell cycle arrest
- essential oil