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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
Analytical method of measuring tea catechins in human plasma by solid-phase extraction and HPLC with electrochemical detection.
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
Deodorizing effects of tea catechins on amines and ammonia.
2002 Feb
Biological activity of phenolic compounds from Alchornea glandulosa.
2004 Jun
[Chemical constitutents of Bauhinia aurea].
2006 Dec
Isolation of the active compound in Mauria heterophylla, a Peruvian plant with antibacterial activity.
2006 Feb
Antibacterial phenolic compounds from the spines of Gleditsia sinensis Lam.
2007 Apr
Anti-HSV-1 and anti-HIV-1 activity of gallic acid and pentyl gallate.
2008 Aug
Antioxidant constituents of Nymphaea caerulea flowers.
2008 Jul
Antiplasmodial phenolic compounds from Piptadenia pervillei.
2008 Mar
[Studies on chemical constituents from leaves of Lysidice brevicalyx].
2008 Nov
Validated HPLC method for the standardization of Phyllanthus niruri (herb and commercial extracts) using corilagin as a phytochemical marker.
2009 Jun
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
LC-MS/MS method for the simultaneous determination of ethyl gallate and its major metabolite in rat plasma.
2010 May
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
  • Download
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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