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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
Structure of ETHYL GALLATE

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

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Inhibition of human immunodeficiency viral replication by tannins and related compounds.
1992 May
Analytical method of measuring tea catechins in human plasma by solid-phase extraction and HPLC with electrochemical detection.
2001 Dec
Ethyl m-digallate from red maple, Acer rubrum L., as the major resistance factor to forest tent caterpillar, Malacosoma disstria Hbn.
2001 Dec
[Polyphenol compounds from Hamamelis virginiana L].
2001 Jan
[Effect of gallic acid derivatives on secretion of Th1 cytokines and Th2 cytokines from anti CD3-stimulated spleen cells].
2001 Jun
Isolation and characterization of novel benzoates, cinnamates, flavonoids, and lignans from Riesling wine and screening for antioxidant activity.
2001 Jun
Free radical lipid peroxidation inhibits enzymatic conversion of beta-carotene into vitamin A.
2001 May
In vitro activity of polyhydroxycarboxylates against herpesviruses and HIV.
2001 Nov
Antioxidant flavonoids and phenolic acids from leaves of Leea guineense G Don (Leeaceae).
2003 Apr
[Studies on the chemical constituents of Ampelopsis humulifolia var. heterophylla (Thunb.) K. Koch].
2003 Sep
[Chemical constitutents of Bauhinia aurea].
2006 Dec
Isolation of the active compound in Mauria heterophylla, a Peruvian plant with antibacterial activity.
2006 Feb
Phosphodiesterase-I inhibitor quinovic acid glycosides from Bridelia ndellensis.
2006 Jun
Antibacterial phenolic compounds from the spines of Gleditsia sinensis Lam.
2007 Apr
Antioxidant activity of brocchlin carboxylic acid and its methyl ester from Chrozophora brocchiana.
2007 Jun
A major ingredient of green tea rescues mice from lethal sepsis partly by inhibiting HMGB1.
2007 Nov 7
Anti-HSV-1 and anti-HIV-1 activity of gallic acid and pentyl gallate.
2008 Aug
Antioxidant constituents of Nymphaea caerulea flowers.
2008 Jul
Recognition and incision of Cr(III) ligand-conjugated DNA adducts by the nucleotide excision repair proteins UvrABC: importance of the Cr(III)-purine moiety in the enzymatic reaction.
2008 Jun
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
Antiplasmodial phenolic compounds from Piptadenia pervillei.
2008 Mar
A new benzofuranic acid from the leaves of Rhus alata.
2008 Mar 20
[Studies on chemical constituents from leaves of Lysidice brevicalyx].
2008 Nov
[Studies on chemical constituents of Salacia prinoides].
2008 Sep
Validated HPLC method for the standardization of Phyllanthus niruri (herb and commercial extracts) using corilagin as a phytochemical marker.
2009 Jun
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
[Chemical constituents from roots of Distylium myricoides].
2009 Sep
The Digital Bee Brain: Integrating and Managing Neurons in a Common 3D Reference System.
2010
Mangifera indica (mango).
2010 Jan
LC-MS/MS method for the simultaneous determination of ethyl gallate and its major metabolite in rat plasma.
2010 May
[Study on the chemical constituents from fresh roots of Euphorbia fischeriana].
2010 Sep
Therapeutic Potential of Plants as Anti-microbials for Drug Discovery.
2010 Sep
Partial least squares and principal components analysis of wine vintage by high performance liquid chromatography with chemiluminescence detection.
2010 Sep 23
Patents
Name Type Language
ETHYL GALLATE
INCI   MART.  
INCI  
Official Name English
NSC-402626
Code English
ETHYL GALLATE [MART.]
Common Name English
ETHYL GALLATE [INCI]
Common Name English
Code System Code Type Description
NSC
402626
Created by admin on Fri Dec 15 18:34:44 GMT 2023 , Edited by admin on Fri Dec 15 18:34:44 GMT 2023
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ECHA (EC/EINECS)
212-608-5
Created by admin on Fri Dec 15 18:34:44 GMT 2023 , Edited by admin on Fri Dec 15 18:34:44 GMT 2023
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WIKIPEDIA
ETHYL GALLATE
Created by admin on Fri Dec 15 18:34:44 GMT 2023 , Edited by admin on Fri Dec 15 18:34:44 GMT 2023
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EPA CompTox
DTXSID2061195
Created by admin on Fri Dec 15 18:34:44 GMT 2023 , Edited by admin on Fri Dec 15 18:34:44 GMT 2023
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EVMPD
SUB174350
Created by admin on Fri Dec 15 18:34:44 GMT 2023 , Edited by admin on Fri Dec 15 18:34:44 GMT 2023
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FDA UNII
235I6UDD3L
Created by admin on Fri Dec 15 18:34:44 GMT 2023 , Edited by admin on Fri Dec 15 18:34:44 GMT 2023
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SMS_ID
100000161045
Created by admin on Fri Dec 15 18:34:44 GMT 2023 , Edited by admin on Fri Dec 15 18:34:44 GMT 2023
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PUBCHEM
13250
Created by admin on Fri Dec 15 18:34:44 GMT 2023 , Edited by admin on Fri Dec 15 18:34:44 GMT 2023
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CAS
831-61-8
Created by admin on Fri Dec 15 18:34:44 GMT 2023 , Edited by admin on Fri Dec 15 18:34:44 GMT 2023
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MESH
C048734
Created by admin on Fri Dec 15 18:34:44 GMT 2023 , Edited by admin on Fri Dec 15 18:34:44 GMT 2023
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