Botanical Source
The Botanical Source category encompasses a diverse range of plant-derived compounds and extracts used in research and product development. These botanical sources include various herbs, trees, and shrubs that provide bioactive compounds for use in pharmaceuticals, cosmetics, and nutritional supplements. At CymitQuimica, we offer a comprehensive selection of botanical sources to support research in natural product chemistry, pharmacology, and traditional medicine.
Found 1459 products of "Botanical Source"
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Linderalactone
CAS:Linderalactone shows significant inhibitory effects on superoxide anion generation by human neutrophils in response to fMLP/CB, the IC50 is 8.48 microg/mL.Formula:C15H16O3Purity:95%~99%Color and Shape:Cryst.Molecular weight:244.29Hinokiflavone
CAS:Hinokiflavone has significant cytotoxicity, it has inhibition of MMP-9.Formula:C30H18O10Purity:95%~99%Molecular weight:538.464Onjisaponin B
CAS:Onjisaponin B, derived from Radix Polygalae, can enhances autophagy and accelerates the degradation of mutant α-synuclein and huntingtin in PC-12 cells.Formula:C75H112O35Purity:95%~99%Color and Shape:PowderMolecular weight:1573.69(-)-Epigallocatechin-3-(3''-O-methyl) gallate
CAS:Formula:C23H20O11Purity:95%~99%Color and Shape:PowderMolecular weight:472.4022''-Rhamnosylvitexin
CAS:Vitexin-2''-O-rhamnoside contributes to the protection against H₂O₂ -mediated oxidative stress damage and could be safely used for a wide range of concentrations.It has low bioavailability, mainly related to its poor absorption in the intestine.Formula:C27H30O14Purity:95%~99%Molecular weight:578.523Liquiritigenin
CAS:Liquiritigenin, an aglycone of liquiritin in G. radix , exerts cytoprotective effects against heavy metal-induced toxicity in vitro, can protect the liver from acute injuries induced by APAP or from APAP-induced severe injuries during GSH deficiency.Formula:C15H12O4Purity:95%~99%Color and Shape:Cryst.Molecular weight:256.257
