Drasar, Pavel B.||Khripach, Vladimir A.

Synthesis, Study and Utilization of Natural Products


English[eng]


varioxiranol A||natural enantiomer||n/a||ribosomally synthesized||triterpenoids||apo-CpcB||water resistance||radical scavenger||bardoxolone methyl||antioxidant activity||octadecanoid||derivatives||inhibitor||chlorogenic acid||biosynthesis||microbial biosynthesis||flow cytometry||adhesive||phycocyanin||antioxidant||anticancer drug||resource chemistry||ginkgolide||anti-inflammation||salt stress||polyphenol||synthesis of natural products||rheumatoid arthritis||PEGylated purpurin 18||photosensitizer||RiPP||isosorbide||bioactivity||cell opening||stilbene||tea tussock moth||flavonoids||flexible polyurethane foam||gene expression||genetical transformation||research progress||oleic acid-elicited||pharmacokinetic features||phenolic acid||Plantago depressa||platelet-activating factor receptor||photodynamic therapy||fatty acid||soy protein isolate||apoptosis||HepG2 cells||cancer cells||live-cell fluorescence microscopy||tomato||caffeoylquinic acids||pinocembrin||insect sex pheromone||4-epi-varioxiranol A||natural products||singlet oxygen||total synthesis||lipid-lowering effects||reversible urethane linkages||cytotoxicity||bromelain||Ramulus mori||polysaccharides||SlCOMT1||pharmacological activities||absolute structure||natural product||mitochondria||Emericella variecolor||triglycidylamine||Spirulina||viscosity||post-translationally modified peptides||phototoxicity||melatonin