A polyphenol flavonoid
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(±)-Catechin (hydrate)

Item No. 29175

Technical Information
Formal Name
(2R,3S)-rel-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol, hydrate
Molecular Formula
C15H14O6 • XH2O
Formula Weight
Purity
≥98%
A solid
DMF: 25 mg/mlDMSO: 10 mg/mlEthanol: 5 mg/mlPBS (pH 7.2): 1 mg/ml
λmax
279 nm
SMILES
OC1=CC(O)=C(C[C@H](O)[C@@H](C2=CC=C(O)C(O)=C2)O3)C3=C1.O
InChi Code
InChI=1S/C15H14O6.H2O/c16-8-4-11(18)9-6-13(20)15(21-14(9)5-8)7-1-2-10(17)12(19)3-7;/h1-5,13,15-20H,6H2;1H2/t13-,15+;/m0./s1
InChi Key
OFUMQWOJBVNKLR-NQQJLSKUSA-N
Origin
Plant/Green tea
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    (±)-Catechin is a polyphenol flavonoid that has been found in C. sinensis leaves and has antioxidant and enzyme inhibitory activities.1,2,3 It reduces iron- and ascorbate-induced lipid peroxidation of isolated bovine brain phospholipid liposomes with an IC50 value of 20 µM in a cell-free assay.2 (±)-Catechin (20 µM) inhibits hepatitis C virus (HCV) RNA-dependent RNA polymerase (RdRp) by 17.7% in an enzyme assay.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Li, Q., Li, J., Liu, S., et alA comparative proteomic analysis of the buds and the young expanding leaves of the tea plant (Camellia Sinensis L.). Comparative Study 16(6), 14007-14038 (2015).

    2. Scott, B.C., Butler, J., Halliwell, B., et alEvaluation of the antioxidant actions of ferulic acid and catechins. Free Radic. Res. Commun. 19(4), 241-253 (1993).

    3. Ahmed-Belkacem, A., Guichou, J.-F., Brillet, R., et alInhibition of RNA binding to hepatitis C virus RNA-dependent RNA polymerase: A new mechanism for antiviral intervention. Nucleic Acids Res. 42(14), 9399-9409 (2014).