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 |
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Molecular mechanisms controlling the rate and specificity of catechol O-methylation by human soluble catechol O-methyltransferase. | 2001 Feb |
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Antioxidant activity of phenolic and related compounds: a density functional theory study on the O-H bond dissociation enthalpy. | 2004 |
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Genetic and biochemical investigations on bacterial catabolic pathways for lignin-derived aromatic compounds. | 2007 Jan |
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Biotransformation of gallic acid by Beauveria sulfurescens ATCC 7159. | 2007 Mar |
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Degradation of 3-O-methylgallate in Sphingomonas paucimobilis SYK-6 by pathways involving protocatechuate 4,5-dioxygenase. | 2007 Sep |
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Identification of Cabernet Sauvignon anthocyanin gut microflora metabolites. | 2008 Oct 8 |
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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 Nov |
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Comparative genome analysis provides insights into the evolution and adaptation of Pseudomonas syringae pv. aesculi on Aesculus hippocastanum. | 2010 Apr 19 |
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Gut metabolites of anthocyanins, gallic acid, 3-O-methylgallic acid, and 2,4,6-trihydroxybenzaldehyde, inhibit cell proliferation of Caco-2 cells. | 2010 May 12 |
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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