G6782

(−)-Gallocatechin gallate

from green tea, ≥98% (HPLC)

Manufacturer: Sigma Aldrich

CAS Number: 4233-96-9

Synonym(S): (2S,3R)-2-(3,4,5-Trihydroxyphenyl)-3,4-dihydro-1(2H)-benzopyran-3,5,7-triol 3-(3,4,5-trihydroxybenzoate)

Select a Size

Pack Size SKU Availability Price
5 MG G6782-5-MG In Stock ₹ 19,885.53

G6782 - 5 MG

₹ 19,885.53

In Stock

Quantity

1

Base Price: ₹ 19,885.53

GST (18%): ₹ 3,579.395

Total Price: ₹ 23,464.925

biological source

green tea

Quality Level

200

Assay

≥98% (HPLC)

form

powder

application(s)

metabolomicsvitamins, nutraceuticals, and natural products

storage temp.

2-8°C

SMILES string

Oc1cc(O)c2C[C@@H](OC(=O)c3cc(O)c(O)c(O)c3)[C@@H](Oc2c1)c4cc(O)c(O)c(O)c4

InChI

1S/C22H18O11/c23-10-5-12(24)11-7-18(33-22(31)9-3-15(27)20(30)16(28)4-9)21(32-17(11)6-10)8-1-13(25)19(29)14(26)2-8/h1-6,18,21,23-30H,7H2/t18-,21+/m1/s1

InChI key

WMBWREPUVVBILR-NQIIRXRSSA-N

Description

  • General description: (−)-Gallocatechin gallate is a polyphenolic compound having a galloyl moiety.[1] It is an epimerized form of epigallocatechin gallate, which is common tea catechin. Epimerization of tea catechins is common upon heat treatment or pasteurization process.[2]
  • Application: (−)-Gallocatechin gallate has been used:to perform the tannase activity assay of the recombinant Lactobacillus plantarum tannase enzyme[3]to study its inhibitory effects on HIV-1 integrase activity [1]to study its regulatory mechanism on cholesterol metabolism in rat liver[4]to analyze its effect as a polyphenol on human spermatozoa and their application in assisted reproductive technology[5]to study the interference in stress protective activity of cellular prion protein (PrPC) and the formation of scrapie prion protein (PrPSc)[6]
  • Biochem/physiol Actions: Tea catechins like (−)-Gallocatechin gallate are known to have antiviral, antioxidative, antimutagenic and antiobesity activities.[2] It exhibits human immunodeficiency virus-1 (HIV-1) integrase inhibitory activity by disturbing the interaction between the human immunodeficiency virus-1 (HIV-1) integrase and virus DNA.[1] GCG also shows impeding effect on the release of vero toxins (VTs) by enterohemorrhagic Escherichia coli.[7] It displays an inhibitory effect on cholesterol absorption and is reported to be more effective than tea catechins in lowering plasma cholesterol, thus preventing atherosclerosis.[2]

SAFETY INFORMATION

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Precautionary Statements

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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200

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Oc1cc(O)c2C[C@@H](OC(=O)c3cc(O)c(O)c(O)c3)[C@@H](Oc2c1)c4cc(O)c(O)c(O)c4

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1S/C22H18O11/c23-10-5-12(24)11-7-18(33-22(31)9-3-15(27)20(30)16(28)4-9)21(32-17(11)6-10)8-1-13(25)19(29)14(26)2-8/h1-6,18,21,23-30H,7H2/t18-,21+/m1/s1

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WMBWREPUVVBILR-NQIIRXRSSA-N

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ATFVTAOSZBVGHC-UHFFFAOYSA-N