L-Epicatechin

L-Epicatechin Basic information
Product Name:L-Epicatechin
Synonyms:3,3′,4′,5,7-PENTAHYDROXY-FLAVANE;3,3′,4′,5,7-PENTAHYROXYFLAVONE;3,3′,4′,5,7-PENTAHYDROXYFLAVAN;(-)-epicatecho;(-)-epicatechol;(+)-EPICATECHIN;EPICATECHIN, (+)-;CIS-2-[3,4-DIHYDROXYPHENYL]-3,4-DIHYDRO-2H-1-BENZOPYRAN-3,5,7-TRIOL
CAS:490-46-0
MF:C15H14O6
MW:290.27
EINECS:207-710-1
Product Categories:chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Pharmaceutical Raw Materials;Aromatics;Chiral Reagents;Inhibitors;Intermediates & Fine Chemicals;Pharmaceuticals;chiral;490-46-0
Mol File:490-46-0.mol
L-Epicatechin Structure
L-Epicatechin Chemical Properties
Melting point 240 °C (dec.)(lit.)
alpha -55~-65゜(D/20℃)(c=1,CH3OH)
Boiling point 629.2 °C
density 1.593±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility insoluble in H2O; insoluble in EtOH; ≥14.5 mg/mL in DMSO
form neat
pka9.54±0.10(Predicted)
color White to Light yellow to Light orange
Water Solubility Soluble in water or alcohol
Merck 13,1912
BRN 92760
Stability:Hygroscopic
InChIKeyPFTAWBLQPZVEMU-UKRRQHHQSA-N
LogP0.490 (est)
CAS DataBase Reference490-46-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
RTECS KB3745000
10-23
HS Code 29329990
MSDS Information
ProviderLanguage
L-EpicatechinEnglish
SigmaAldrichEnglish
L-Epicatechin Usage And Synthesis
Description(−)-Epicatechin is a polyketide synthase-derived polyphenol flavonoid that has been found in T. cacao and has diverse biological activities. It scavenges DPPH radicals in a cell-free assay when used at a concentration of 5 μM. (−)-Epicatechin inhibits COX-1 (IC50 = 3.2 μM). It acts synergistically with epigallocatechin gallate to induce apoptosis in, and reduce the proliferation of, PC-9 lung cancer cells when used at a concentration of 200 μM. (−)-Epicatechin (80 mg/kg) reduces LPS-induced increases in plasma creatinine and urea levels in a rat model of renal inflammation.
Chemical Propertieswhite to light yellow crystal powde
UsesAn antioxidant and natural product from green tea
UsesCatechin is a polyphenolic flavonoid that has been isolated from a variety of natural sources including tea leaves, grape seeds, and the wood and bark of trees such as acacia and mahogany. Catechin is a more potent antioxidant than ascorbate or α-tocopherol in certain in vitro lipid peroxidation assays. (?)-Epicatechin is a 2R,3R stereoisomer of catechin. Like catechin, (?)-epicatechin is a powerful antioxidant. It inhibits cyclooxygenase 1 (IC50 = 3.2 μM). Also, at 100 μM, (?)-epicatechin induces apoptosis in human adenocarcinoma PC-9 cells and stimulates the inhibition of tumor necrosis factor-α release from BALB-c/3T3 cells treated with epigallocatechin gallate.
UsesPotent antioxidant and antineoplastic agent.
DefinitionChEBI: A catechin with (2R,3R)-configuration.
General Description(?)-Epicatechin (EC) belongs to the group of flavanols and is abundantly present in cacao and cacao products. The chemical structure of EC includes an oxygenated heterocycle with a 4-hydroxyl group linked with two aromatic rings.
Biochem/physiol ActionsThis antioxidant is found in chocolate. (-)-Epicatechin is linked with cardiovascular effects. It is considered as a dependable standard due to its availability in cacao seeds and cocoa products. The halogenating activity of myeloperoxidase can be restored by (-)-epicatechin.
references[1]. chakravarthy bk, gupta s, gambhir ss, et al. pancreatic beta-cell regeneration in rats by (-)-epicatechin. lancet, 1981, 2(8249): 759-760.
[2]. wippel r, rehn m, gorren ac, et al. interference of the polyphenol epicatechin with the biological chemistry of nitric oxide- and peroxynitrite-mediated reactions. biochem pharmacol, 2004, 67(7): 1285-1295.
[3]. brossette t, hundsdörfer c, kröncke kd, et al. direct evidence that (-)-epicatechin increases nitric oxide levels in human endothelial cells. eur j nutr, 2011, 50(7): 595-599.
[4]. okushio k, suzuki m, matsumoto n, et al. identification of (-)-epicatechin metabolites and their metabolic fate in the rat. drug metab dispos, 1999, 27(2): 309-316.
L-Epicatechin Preparation Products And Raw materials
Preparation ProductsProcyanidin B1

دیدگاهی بنویسید

نشانی ایمیل شما منتشر نخواهد شد. بخش‌های موردنیاز علامت‌گذاری شده‌اند *