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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

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

PubMed

TitleDatePubMed
Partial least squares and principal components analysis of wine vintage by high performance liquid chromatography with chemiluminescence detection.
2010-09-23
[Study on the chemical constituents from fresh roots of Euphorbia fischeriana].
2010-09
Therapeutic Potential of Plants as Anti-microbials for Drug Discovery.
2010-09
Cell death shapes embryonic lineages of the central complex in the grasshopper Schistocerca gregaria.
2010-08
[Chemical constituents from stem barks of Vernonia cumingiana].
2010-06
LC-MS/MS method for the simultaneous determination of ethyl gallate and its major metabolite in rat plasma.
2010-05
Chemical changes during fermentation of Abhayarishta and its standardization by HPLC-DAD.
2010-04
In vitro drug interactions of gallates with antibiotics in Staphylococcus Aureus.
2010-01-01
Mangifera indica (mango).
2010-01
The Digital Bee Brain: Integrating and Managing Neurons in a Common 3D Reference System.
2010
[Chemical constituents from roots of Distylium myricoides].
2009-09
Validated HPLC method for the standardization of Phyllanthus niruri (herb and commercial extracts) using corilagin as a phytochemical marker.
2009-06
A redetermination of 2-(6-diethyl-amino-3-diethyl-iminio-3H-xanthen-9-yl)benzoate-ethyl gallate (1/1) at room temperature.
2009-03-06
[Studies on chemical constituents from leaves of Lysidice brevicalyx].
2008-11
[Studies on chemical constituents of Salacia prinoides].
2008-09
Anti-HSV-1 and anti-HIV-1 activity of gallic acid and pentyl gallate.
2008-08
Antioxidant constituents of Nymphaea caerulea flowers.
2008-07
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.
2008-06-07
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.
2008-06
A new benzofuranic acid from the leaves of Rhus alata.
2008-03-20
Antiplasmodial phenolic compounds from Piptadenia pervillei.
2008-03
A major ingredient of green tea rescues mice from lethal sepsis partly by inhibiting HMGB1.
2007-11-07
Antioxidant activity of brocchlin carboxylic acid and its methyl ester from Chrozophora brocchiana.
2007-06
Antibacterial phenolic compounds from the spines of Gleditsia sinensis Lam.
2007-04
[Chemical constitutents of Bauhinia aurea].
2006-12
Phosphodiesterase-I inhibitor quinovic acid glycosides from Bridelia ndellensis.
2006-06
Isolation of the active compound in Mauria heterophylla, a Peruvian plant with antibacterial activity.
2006-02
Effects of structure on radical-scavenging abilities and antioxidative activities of tea polyphenols: NMR analytical approach using 1,1-diphenyl-2-picrylhydrazyl radicals.
2005-05-04
Biological activity of phenolic compounds from Alchornea glandulosa.
2004-06
[Studies on the chemical constituents of Ampelopsis humulifolia var. heterophylla (Thunb.) K. Koch].
2003-09
Antioxidant flavonoids and phenolic acids from leaves of Leea guineense G Don (Leeaceae).
2003-04
Two new and four known polyphenolics obtained as new cell-cycle inhibitors from Rubus aleaefolius Poir.
2002-12
GC-mS analysis and anti-microbial activity of acidic fractions obtained from Paeonia peregrina and Paeonia tenuifolia roots.
2002-09-21
Inhibition of cancer cell growth by crude extract and the phenolics of Terminalia chebula retz. fruit.
2002-08
Pharmacologically active ellagitannins from Terminalia myriocarpa.
2002-06
Deodorizing effects of tea catechins on amines and ammonia.
2002-02
Analytical method of measuring tea catechins in human plasma by solid-phase extraction and HPLC with electrochemical detection.
2001-12
Ethyl m-digallate from red maple, Acer rubrum L., as the major resistance factor to forest tent caterpillar, Malacosoma disstria Hbn.
2001-12
In vitro activity of polyhydroxycarboxylates against herpesviruses and HIV.
2001-11
[Effect of gallic acid derivatives on secretion of Th1 cytokines and Th2 cytokines from anti CD3-stimulated spleen cells].
2001-06
Isolation and characterization of novel benzoates, cinnamates, flavonoids, and lignans from Riesling wine and screening for antioxidant activity.
2001-06
Free radical lipid peroxidation inhibits enzymatic conversion of beta-carotene into vitamin A.
2001-05
[Polyphenol compounds from Hamamelis virginiana L].
2001-01
Inhibition of human immunodeficiency viral replication by tannins and related compounds.
1992-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:15:50 GMT 2025
Edited
by admin
on Mon Mar 31 19:15:50 GMT 2025
Record UNII
235I6UDD3L
Record Status Validated (UNII)
Record Version
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Name Type Language
NSC-402626
Preferred Name English
ETHYL GALLATE
INCI   MART.  
INCI  
Official Name English
ETHYL GALLATE [MART.]
Common Name English
Code System Code Type Description
NSC
402626
Created by admin on Mon Mar 31 19:15:50 GMT 2025 , Edited by admin on Mon Mar 31 19:15:50 GMT 2025
PRIMARY
ECHA (EC/EINECS)
212-608-5
Created by admin on Mon Mar 31 19:15:50 GMT 2025 , Edited by admin on Mon Mar 31 19:15:50 GMT 2025
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WIKIPEDIA
ETHYL GALLATE
Created by admin on Mon Mar 31 19:15:50 GMT 2025 , Edited by admin on Mon Mar 31 19:15:50 GMT 2025
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EPA CompTox
DTXSID2061195
Created by admin on Mon Mar 31 19:15:50 GMT 2025 , Edited by admin on Mon Mar 31 19:15:50 GMT 2025
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EVMPD
SUB174350
Created by admin on Mon Mar 31 19:15:50 GMT 2025 , Edited by admin on Mon Mar 31 19:15:50 GMT 2025
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FDA UNII
235I6UDD3L
Created by admin on Mon Mar 31 19:15:50 GMT 2025 , Edited by admin on Mon Mar 31 19:15:50 GMT 2025
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SMS_ID
100000161045
Created by admin on Mon Mar 31 19:15:50 GMT 2025 , Edited by admin on Mon Mar 31 19:15:50 GMT 2025
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PUBCHEM
13250
Created by admin on Mon Mar 31 19:15:50 GMT 2025 , Edited by admin on Mon Mar 31 19:15:50 GMT 2025
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CAS
831-61-8
Created by admin on Mon Mar 31 19:15:50 GMT 2025 , Edited by admin on Mon Mar 31 19:15:50 GMT 2025
PRIMARY
MESH
C048734
Created by admin on Mon Mar 31 19:15:50 GMT 2025 , Edited by admin on Mon Mar 31 19:15:50 GMT 2025
PRIMARY