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Gallocatechin gallate
🥰Excellent
Catalog No. TN4094Cas No. 5127-64-0
Alias 3-O-Galloyl-(+)-gallocatechin, (+)-Gallocatechin gallate
Gallocatechin gallate is a flavonoid compound isolated from South American snake plant, with antiviral activity by inhibiting the entry and release stages of pseudorabies virus replication.
Gallocatechin gallate
🥰Excellent
Catalog No. TN4094Alias 3-O-Galloyl-(+)-gallocatechin, (+)-Gallocatechin gallateCas No. 5127-64-0
Gallocatechin gallate is a flavonoid compound isolated from South American snake plant, with antiviral activity by inhibiting the entry and release stages of pseudorabies virus replication.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $80 | In Stock | |
| 5 mg | $176 | In Stock | |
| 10 mg | $264 | In Stock |
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Product Introduction
Bioactivity
Chemical Properties
| Description | Gallocatechin gallate is a flavonoid compound isolated from South American snake plant, with antiviral activity by inhibiting the entry and release stages of pseudorabies virus replication. |
| Targets&IC50 | SARS-CoV-2:5.774 μM, PRV:0.41 μM |
| In vitro | Gallocatechin gallate effectively inhibited the replication of Pseudorabies virus (PRV) with IC50 of 0.41 μM. [1] Gallocatechin gallate showed effective inhibitory activity against SARS-CoV-2 with IC50 of 5.774 μM. [4] |
| In vivo | Gallocatechin gallate (100 mg/kg/ day for 20 weeks) and water administration, which resulted in a significant reduction in food consumption and water intake in db/db mice, had the ability to prevent excessive weight gain in db/db mice. [2] Gallocatechin gallate is presented in three dose levels (12.5 mg/mL; 25 mg/mL; Mice irradiated with UVB once daily for 6 days showed that Gallocatechin gallate protects the skin from UVB-induced light damage by improving skin elasticity and collagen fibers, inhibiting mitochondrial aberration and melansome formation. [3] |
| Alias | 3-O-Galloyl-(+)-gallocatechin, (+)-Gallocatechin gallate |
| Molecular Weight | 458.37 |
| Formula | C22H18O11 |
| Cas No. | 5127-64-0 |
| Smiles | O(C(=O)C1=CC(O)=C(O)C(O)=C1)[C@@H]2[C@H](OC=3C(C2)=C(O)C=C(O)C3)C4=CC(O)=C(O)C(O)=C4 |
| Relative Density. | 1.90 g/cm3 (Predicted) |
Storage & Solubility Information
| Storage | keep away from moisture,keep away from direct sunlight,store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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