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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
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
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
Inhibition of cancer cell growth by crude extract and the phenolics of Terminalia chebula retz. fruit.
2002 Aug
Two new and four known polyphenolics obtained as new cell-cycle inhibitors from Rubus aleaefolius Poir.
2002 Dec
GC-mS analysis and anti-microbial activity of acidic fractions obtained from Paeonia peregrina and Paeonia tenuifolia roots.
2002 Jul-Aug
Pharmacologically active ellagitannins from Terminalia myriocarpa.
2002 Jun
Antioxidant flavonoids and phenolic acids from leaves of Leea guineense G Don (Leeaceae).
2003 Apr
Biological activity of phenolic compounds from Alchornea glandulosa.
2004 Jun
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
Isolation of the active compound in Mauria heterophylla, a Peruvian plant with antibacterial activity.
2006 Feb
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
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
[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
Cell death shapes embryonic lineages of the central complex in the grasshopper Schistocerca gregaria.
2010 Aug
Mangifera indica (mango).
2010 Jan
In vitro drug interactions of gallates with antibiotics in Staphylococcus Aureus.
2010 Jan 1
[Chemical constituents from stem barks of Vernonia cumingiana].
2010 Jun
[Study on the chemical constituents from fresh roots of Euphorbia fischeriana].
2010 Sep
Partial least squares and principal components analysis of wine vintage by high performance liquid chromatography with chemiluminescence detection.
2010 Sep 23
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:34:44 GMT 2023
Edited
by admin
on Fri Dec 15 18:34:44 GMT 2023
Record UNII
235I6UDD3L
Record Status Validated (UNII)
Record Version
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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
PRIMARY
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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