Details
Stereochemistry | ACHIRAL |
Molecular Formula | C9H10O5 |
Molecular Weight | 198.1727 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(=O)C1=CC(O)=C(O)C(O)=C1
InChI
InChIKey=VFPFQHQNJCMNBZ-UHFFFAOYSA-N
InChI=1S/C9H10O5/c1-2-14-9(13)5-3-6(10)8(12)7(11)4-5/h3-4,10-12H,2H2,1H3
Molecular Formula | C9H10O5 |
Molecular Weight | 198.1727 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
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Inhibition of human immunodeficiency viral replication by tannins and related compounds. | 1992 May |
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Analytical method of measuring tea catechins in human plasma by solid-phase extraction and HPLC with electrochemical detection. | 2001 Dec |
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Ethyl m-digallate from red maple, Acer rubrum L., as the major resistance factor to forest tent caterpillar, Malacosoma disstria Hbn. | 2001 Dec |
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[Polyphenol compounds from Hamamelis virginiana L]. | 2001 Jan |
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Isolation and characterization of novel benzoates, cinnamates, flavonoids, and lignans from Riesling wine and screening for antioxidant activity. | 2001 Jun |
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Free radical lipid peroxidation inhibits enzymatic conversion of beta-carotene into vitamin A. | 2001 May |
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In vitro activity of polyhydroxycarboxylates against herpesviruses and HIV. | 2001 Nov |
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Inhibition of cancer cell growth by crude extract and the phenolics of Terminalia chebula retz. fruit. | 2002 Aug |
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Two new and four known polyphenolics obtained as new cell-cycle inhibitors from Rubus aleaefolius Poir. | 2002 Dec |
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GC-mS analysis and anti-microbial activity of acidic fractions obtained from Paeonia peregrina and Paeonia tenuifolia roots. | 2002 Jul-Aug |
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Pharmacologically active ellagitannins from Terminalia myriocarpa. | 2002 Jun |
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Antioxidant flavonoids and phenolic acids from leaves of Leea guineense G Don (Leeaceae). | 2003 Apr |
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Biological activity of phenolic compounds from Alchornea glandulosa. | 2004 Jun |
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Effects of structure on radical-scavenging abilities and antioxidative activities of tea polyphenols: NMR analytical approach using 1,1-diphenyl-2-picrylhydrazyl radicals. | 2005 May 4 |
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Isolation of the active compound in Mauria heterophylla, a Peruvian plant with antibacterial activity. | 2006 Feb |
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Antioxidant activity of brocchlin carboxylic acid and its methyl ester from Chrozophora brocchiana. | 2007 Jun |
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A major ingredient of green tea rescues mice from lethal sepsis partly by inhibiting HMGB1. | 2007 Nov 7 |
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Anti-HSV-1 and anti-HIV-1 activity of gallic acid and pentyl gallate. | 2008 Aug |
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Antioxidant constituents of Nymphaea caerulea flowers. | 2008 Jul |
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A low-temperature phase of the 1:1 complex of 2-(6-diethylamino-3-diethyl-iminio-3H-xanthen-9-yl)benzoate with ethyl gallate at 93 K. | 2008 Jun 7 |
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[Studies on chemical constituents from leaves of Lysidice brevicalyx]. | 2008 Nov |
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[Studies on chemical constituents of Salacia prinoides]. | 2008 Sep |
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Validated HPLC method for the standardization of Phyllanthus niruri (herb and commercial extracts) using corilagin as a phytochemical marker. | 2009 Jun |
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A redetermination of 2-(6-diethyl-amino-3-diethyl-iminio-3H-xanthen-9-yl)benzoate-ethyl gallate (1/1) at room temperature. | 2009 Mar 6 |
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[Chemical constituents from roots of Distylium myricoides]. | 2009 Sep |
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The Digital Bee Brain: Integrating and Managing Neurons in a Common 3D Reference System. | 2010 |
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Cell death shapes embryonic lineages of the central complex in the grasshopper Schistocerca gregaria. | 2010 Aug |
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Mangifera indica (mango). | 2010 Jan |
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In vitro drug interactions of gallates with antibiotics in Staphylococcus Aureus. | 2010 Jan 1 |
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[Chemical constituents from stem barks of Vernonia cumingiana]. | 2010 Jun |
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[Study on the chemical constituents from fresh roots of Euphorbia fischeriana]. | 2010 Sep |
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Partial least squares and principal components analysis of wine vintage by high performance liquid chromatography with chemiluminescence detection. | 2010 Sep 23 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:34:44 GMT 2023
by
admin
on
Fri Dec 15 18:34:44 GMT 2023
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Record UNII |
235I6UDD3L
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Record Status |
Validated (UNII)
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Record Version |
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402626
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212-608-5
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ETHYL GALLATE
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DTXSID2061195
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SUB174350
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235I6UDD3L
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100000161045
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13250
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831-61-8
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C048734
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