Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H8O5 |
| Molecular Weight | 184.1461 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(O)C(O)=CC(=C1)C(O)=O
InChI
InChIKey=KWCCUYSXAYTNKA-UHFFFAOYSA-N
InChI=1S/C8H8O5/c1-13-6-3-4(8(11)12)2-5(9)7(6)10/h2-3,9-10H,1H3,(H,11,12)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Gut metabolites of anthocyanins, gallic acid, 3-O-methylgallic acid, and 2,4,6-trihydroxybenzaldehyde, inhibit cell proliferation of Caco-2 cells. | 2010-05-12 |
|
| Comparative genome analysis provides insights into the evolution and adaptation of Pseudomonas syringae pv. aesculi on Aesculus hippocastanum. | 2010-04-19 |
|
| Anti-ischemic activity and endothelium-dependent vasorelaxant effect of hydrolysable tannins from the leaves of Rhus coriaria (Sumac) in isolated rabbit heart and thoracic aorta. | 2009-11 |
|
| Identification of Cabernet Sauvignon anthocyanin gut microflora metabolites. | 2008-10-08 |
|
| Degradation of 3-O-methylgallate in Sphingomonas paucimobilis SYK-6 by pathways involving protocatechuate 4,5-dioxygenase. | 2007-09 |
|
| Biotransformation of gallic acid by Beauveria sulfurescens ATCC 7159. | 2007-03 |
|
| Genetic and biochemical investigations on bacterial catabolic pathways for lignin-derived aromatic compounds. | 2007-01 |
|
| Antioxidant activity of phenolic and related compounds: a density functional theory study on the O-H bond dissociation enthalpy. | 2004 |
|
| Molecular mechanisms controlling the rate and specificity of catechol O-methylation by human soluble catechol O-methyltransferase. | 2001-02 |
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3934-84-7
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223-512-8
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28647
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8JA4OZ7166
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19829
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DTXSID10192561
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C025525
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SUBSTANCE RECORD
