Structure via PubChem · Public domain (PubChem)
Chemical data
- Formula
- C14H10O9
- Molecular weight
- 322.22 g/mol
- IUPAC name
- 3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoic acid
- SMILES
- C1=C(C=C(C(=C1O)O)O)C(=O)OC2=CC(=CC(=C2O)O)C(=O)O
- InChIKey
- COVFEVWNJUOYRL-UHFFFAOYSA-N
- XLogP
- 1.1
- Polar surface area
- 165 Ų
- H-bond donors
- 6
- H-bond acceptors
- 9
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
41 papers- Discovery of digallic acid as XOD/URAT1 dual target inhibitor for the treatment of hyperuricemia.Bioorganic chemistry · 2024
- Digallic acid from Pistascia lentiscus fruits induces apoptosis and enhances antioxidant activities.Phytotherapy research : PTR · 2012
- Potent Inhibition of Bacterial DNA Gyrase by Digallic Acid and Other Gallate Derivatives.ChemMedChem · 2022
- Quinic and Digallic acids from Pistacia atlantica Desf. Leaves Extracts as Potent Dual Effect Inhibitors against main Protease and RNA-dependent RNA Polymerase of SARS-CoV-2.Current computer-aided drug design · 2022
- Differential inhibition of reverse transcriptase and various DNA polymerases by digallic acid and its derivatives.Journal of natural products · 1990
via PubMed
Wikidata facts
- Subclass of
- depside
- Mass
- 322.032
Show 5 more facts
- found in taxon
- Rhus chinensis
- Commons category
- Digallic acid
- chemical formula
- C₁₄H₁₀O₉
- canonical SMILES
- C1=C(C=C(C(=C1O)O)O)C(=O)OC2=CC(=CC(=C2O)O)C(=O)O
- subject has role
- DNA polymerase inhibitors
Sources (2)
via Wikidata · CC0