
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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Apigenin-7-O -(2G-rhamnosyl)gentiobioside
CAS:Formula:C33H40O19Purity:95%~99%Molecular weight:740.664Periplogenin 3-[O-β-glucopyranosyl-(1→4)-β-sarmentopyranoside]
CAS:Formula:C36H56O13Purity:95%~99%Molecular weight:696.831Genistein
CAS:Genistein, the major phytoestrogen in soy, is linked to diminished female reproductive performance and to cancer chemoprevention and decreased adipose deposition; genistein-induces hypermethylation persisted into adulthood, decreases ectopic Agouti expression and protecting offspring from obesity, suggests that in utero dietary genistein affects gene expression and alters susceptibility to obesity in adulthood by permanently altering the epigenome.Formula:C15H10O5Purity:95%~99%Color and Shape:Yellow powderMolecular weight:270.24Catechin gallate
CAS:Catechin gallate is a minor constituent in green tea catechins, it inhibits the activity of COX-1 and COX-2 enzymes. Catechin gallate (IC50=53 microM) shows cytotoxicity against the colorectal adenocarcinoma cell line HCT116, it also exhibits strong anti-proliferative and anti-inflammatory activities on pancreatic ductal adenocarcinoma (PDAC) cells. Catechin 3-gallate is a good inhibitor of maltase, with IC50 values of 62 uM, it inhibits both α-glucosidases and rabbit glycogen phosphorylase (GP) in vitro and in cell culture, would contribute to the protection or improvement of type 2 diabetes.Formula:C22H18O10Purity:95%~99%Molecular weight:442.376Chrysosplenetin B
CAS:Chrysosplenetin is a metabolic inhibitor of artemisinin, it has strong activity in vitro against EV71 with low cytotoxicity. Co-administration of artemisinin(ART) with chrysosplenetin(CHR) in ratio of 1:2 achieved a synergic anti-malarial effect partly because of the noncompetitive or uncompetitive inhibition of CHR of drug-metabolism enzymes, especially CYP3A which is closely related to the auto-induction of ART.Formula:C19H18O8Purity:95%~99%Molecular weight:374.345
