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(-)-Gallocatechin gallate

Catalog No. T3807   CAS 4233-96-9
Synonyms: (-)-gallocatechin-3-O-gallate, (-)-Gallocatechol gallate, Gallocatechin gallate

(-)-Gallocatechin gallate ((-)-gallocatechin-3-O-gallate) is the polyphenol isolated from tea, with cancer-preventive activities. (-)-Gallocatechin gallate decreases osteoclastogenesis at 20 microM.

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(-)-Gallocatechin gallate Chemical Structure
(-)-Gallocatechin gallate, CAS 4233-96-9
Pack Size Availability Price/USD Quantity
2 mg In stock $ 39.00
5 mg In stock $ 63.00
10 mg In stock $ 96.00
25 mg In stock $ 195.00
50 mg In stock $ 288.00
100 mg In stock $ 433.00
1 mL * 10 mM (in DMSO) In stock $ 68.00
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Purity: 99.78%
Purity: 99.25%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description (-)-Gallocatechin gallate ((-)-gallocatechin-3-O-gallate) is the polyphenol isolated from tea, with cancer-preventive activities. (-)-Gallocatechin gallate decreases osteoclastogenesis at 20 microM.
Source
Synonyms (-)-gallocatechin-3-O-gallate, (-)-Gallocatechol gallate, Gallocatechin gallate
Molecular Weight 458.37
Formula C22H18O11
CAS No. 4233-96-9

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 82 mg/mL(178.9 mM)

Chloroform, Dichloromethane, Ethyl Acetate, Acetone: Soluble

TargetMolReferences and Literature

1. Ko CH,et al. Effects of tea catechins, epigallocatechin, gallocatechin, and gallocatechin gallate, on bone metabolism. J Agric Food Chem. 2009 Aug 26;57(16):7293-7. 2. Ikeda I,et al. Heat-epimerized tea catechins rich in gallocatechin gallate and catechin gallate are more effective to inhibit cholesterol absorption than tea catechins rich in epigallocatechin gallate and epicatechin gallate. J Agric Food Chem. 2003 Dec 3;51(25):7303-7. 3. Zhao, Ming, et al. GCG inhibits SARS-CoV-2 replication by disrupting the liquid phase condensation of its nucleocapsid protein. Nature Communications . 12.1 (2021): 1-14.

TargetMolCitations

1. Zhao, Ming, et al. GCG inhibits SARS-CoV-2 replication by disrupting the liquid phase condensation of its nucleocapsid protein. Nature Communications. 2021 Apr 9;12(1):2114. doi: 10.1038/s41467-021-22297-8. 2. Xiao T, Cui M, Zheng C, et al. Both Baicalein and Gallocatechin Gallate Efficaciously Inhibit SARS-CoV-2 Replication by Targeting Mpro and Sepsis in Mice. Inflammation. 2021: 1-13. 3. Chen J, Zhou X, Fu L, et al.Natural Product-Based Screening for Lead Compounds Targeting SARS CoV-2 Mpro[J]. Pharmaceuticals, 2023, 16(5): 767..Pharmaceuticals.2023, 16(5): 767.

Related compound libraries

This product is contained In the following compound libraries:
Traditional Chinese Medicine Monomer Library Anti-Cancer Active Compound Library Anti-Cancer Compound Library Food as Medicine Compound Library Natural Product Library for HTS Selected Plant-Sourced Compound Library Traditional Mongolian Medicine Compound Library Chinese Pharmacopoeia Natural Product Library Bioactive Compounds Library Max Natural Product Library

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Keywords

(-)-Gallocatechin gallate 4233-96-9 Others ( ) Gallocatechin gallate (-)-gallocatechin-3-O-gallate Gallocatechol gallate ()Gallocatechin gallate Inhibitor inhibit (-)-Gallocatechol gallate gallocatechin-3-O-gallate Gallocatechin gallate inhibitor

 

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