research use only
Cat.No.S4603
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In vitro |
DMSO
: 34 mg/mL
(199.85 mM)
Ethanol : 34 mg/mL Water : 7 mg/mL |
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In vivo |
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Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
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Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
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| Molecular Weight | 170.12 | Formula | C7H6O5 |
Storage (From the date of receipt) | |
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| CAS No. | 149-91-7 | Download SDF | Storage of Stock Solutions |
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| Synonyms | 3,4,5-Trihydroxybenzoic acid, Gallate, Benzoic acid | Smiles | C1=C(C=C(C(=C1O)O)O)C(=O)O | ||
| In vitro |
Gallic acid does not protect against H(2)O(2)-induced PC12 cell death. It reduced the viability of PC12 cells in a dose-dependent manner. This compound also induces cleavage of poly (ADP-ribose) polymerase, which is strongly related to apoptosis in neurons. It induces the phosphorylation of c-Jun N-terminal protein kinase (JNK) and the downregulation of Bcl-2 in PC12 cells. This chemical leads to a progressive reduction in the viability of vector-transfected PC12 cells, which is delayed in PC12 cells that overexpressed Bcl-2.
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| In vivo |
Gallic acid effectively protects rat erythrocytes. The antioxidant effect of this compound at the tested dosage in vivo was more prevalent than its prooxidative effects. It has ameliorative effect on lipid peroxidation in vivo.
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References |
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(data from https://clinicaltrials.gov, updated on 2024-05-22)
| NCT Number | Recruitment | Conditions | Sponsor/Collaborators | Start Date | Phases |
|---|---|---|---|---|---|
| NCT03413735 | Unknown status | Obesity|Endotoxemia|Inflammation |
Ohio State University |
August 29 2018 | Not Applicable |
| NCT02779361 | Completed | Healthy Volunteers|Doping in Sports |
Parc de Salut Mar|World Anti-Doping Agency |
January 2016 | Phase 1 |
| NCT02008721 | Completed | Multiple System Atrophy |
Dr. Johannes Levin|German Center for Neurodegenerative Diseases (DZNE)|Deutsche Parkinson Vereinigung|German Foundation for Neurology|ParkinsonFonds Deutschland gGmbH|Ludwig-Maximilians - University of Munich |
January 2014 | Phase 3 |
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