CAS 970-73-0: Gallocatechin
Formula:C15H14O7
InChI:InChI=1S/C15H14O7/c16-7-3-9(17)8-5-12(20)15(22-13(8)4-7)6-1-10(18)14(21)11(19)2-6/h1-4,12,15-21H,5H2/t12-,15+/m0/s1
InChI key:InChIKey=XMOCLSLCDHWDHP-SWLSCSKDSA-N
SMILES:O[C@@H]1[C@H](OC=2C(C1)=C(O)C=C(O)C2)C3=CC(O)=C(O)C(O)=C3
Synonyms:- (+)-Gallocatechin
- (2R,3S)-(+)-Gallocatechin
- (2R,3S)-3,4-Dihydro-2-(3,4,5-trihydroxyphenyl)-2H-1-benzopyran-3,5,7-triol
- 2H-1-Benzopyran-3,5,7-triol,3,4-dihydro-2-(3,4,5-trihydroxyphenyl)-, (2R-trans)-
- Gallocatechol
- Gallocatechol, d-
- Nsc 674038
- Sunphenon EGC-OP
- d-Gallocatechin
- 2H-1-Benzopyran-3,5,7-triol, 3,4-dihydro-2-(3,4,5-trihydroxyphenyl)-, (2R,3S)-
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Found 11 products.
2H-1-Benzopyran-3,5,7-triol, 3,4-dihydro-2-(3,4,5-trihydroxyphenyl)-,(2R,3S)-
CAS:Formula:C15H14O7Purity:98%Color and Shape:SolidMolecular weight:306.26745999999997(+)-Gallocatechin
CAS:(+)-Gallocatechin is a flavonoid, which is a type of polyphenol compound, naturally found in a variety of plant sources such as tea leaves, cocoa, and certain fruits. It is structurally related to other catechins, sharing similar properties and biological activities. As an antioxidant, (+)-Gallocatechin acts by scavenging free radicals, thereby inhibiting oxidative stress-a process linked to various chronic diseases and aging. In addition to its antioxidative properties, it plays a role in modulating enzyme activities and signaling pathways. This influence extends into areas such as cholesterol metabolism and immune response modulation. The compound has been explored for its potential applications in cardiovascular health, cancer prevention, and neuroprotective strategies, aligning with a broader interest in dietary polyphenols for health maintenance and disease prevention. Research on (+)-Gallocatechin continues to uncover its complex interactions within biological systems, making it a topic of interest in pharmacology and nutritional science. Its multifaceted roles suggest promising avenues for therapeutic development, although more studies are needed to fully understand its mechanisms and efficacy in clinical settings.Formula:C15H14O7Purity:Min. 95%Molecular weight:306.27 g/mol(+)-Gallocatechin
CAS:(+)-Gallocatechin as a bio-antimutagenic compound against UV-induced mutation in Escherichia coli. It is potent in scavenging Fremy’s salt, a synthetic free radical, it possesses antioxidant capacities that is higher or comparable to that of ascorbic acid or Trolox.Formula:C15H14O7Purity:95%~99%Color and Shape:White powderMolecular weight:306.27(+)-Gallocatechin-13C3
CAS:Controlled ProductFormula:C3C12H14O7Color and Shape:NeatMolecular weight:309.245(+)-Gallocatechin
CAS:(+)-Gallocatechin (Gallocatechol) possesses free radical scavenging ability. (+)-Gallocatechin has moderate affinity to the human cannabinoid receptor.Formula:C15H14O7Purity:98.12% - 99.52%Color and Shape:SolidMolecular weight:306.27(+)-Gallocatechin
CAS:Stability Hygroscopic Applications (+)-Gallocatechin is antioxidant isomer of (-)-Gallocatechin (G188990), a potential cancer chemopreventive agent that inhibits the growth and adherence of P. gingivalis onto the buccal epithelial cells. An epimer of (-)-Epigallocatechin (E588940). References Rychlik, J., et. al: J. Sci. Food Agr., 95, 1892 (2015); Guo, Q. et al.: Biochim. Biophys. Acta, 1427, 13 (1999); Sakanaka, S. et al.: Biosci. Biotechnol. Biochem., 60, 745 (1996)Formula:C15H14O7Color and Shape:White To Light BrownMolecular weight:306.27(+)-Gallocatechin
CAS:(+)-Gallocatechin analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C15H14O7Purity:(HPLC) ≥98%Color and Shape:PowderMolecular weight:306.27(+)-Gallocatechin
CAS:Formula:C15H14O7Purity:≥ 95.0%Color and Shape:White to beige or pale brown powder or solidMolecular weight:306.27
