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Details

Stereochemistry ACHIRAL
Molecular Formula C3H4O5
Molecular Weight 120.0609
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TARTRONIC ACID

SMILES

OC(C(O)=O)C(O)=O

InChI

InChIKey=ROBFUDYVXSDBQM-UHFFFAOYSA-N
InChI=1S/C3H4O5/c4-1(2(5)6)3(7)8/h1,4H,(H,5,6)(H,7,8)

HIDE SMILES / InChI

Molecular Formula C3H4O5
Molecular Weight 120.0609
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Substrate and cofactor binding to fluorescently labeled cytoplasmic malate dehydrogenase.
2001 Feb 9
Relationships between inhibition constants, inhibitor concentrations for 50% inhibition and types of inhibition: new ways of analysing data.
2001 Jul 1
Synthesis, conformational studies, and investigations on the estrogen receptor binding of [R/S-1-(2,6-dichloro-4-hydroxyphenyl)ethylenediamine]platinum(II) complexes.
2001 Mar
Ammonium hydrogen tartronate at 240 and 20 K.
2001 Nov
Molecular mechanism for the regulation of human mitochondrial NAD(P)+-dependent malic enzyme by ATP and fumarate.
2002 Jul
Determination of the side-products formed during the nitroxide-mediated bleach oxidation of glucose to glucaric acid.
2002 Jun 5
Crystallographic studies on Ascaris suum NAD-malic enzyme bound to reduced cofactor and identification of an effector site.
2003 Sep 26
2-Pyridone-tartronic acid (1/1), 3-hydroxypyridinium hydrogen tartronate and 4-hydroxypyridinium hydrogen tartronate.
2004 Oct
Overtone-induced decarboxylation: a potential sink for atmospheric diacids.
2005 Feb 3
Counterion specificity in the phase behavior of tetradecyldimethylamine oxides at different degrees of protonation.
2006 Jul 1
Kinetics and mechanism of degradation of p-chloronitrobenzene in water by ozonation.
2008 Apr 15
A dynamic kinetic asymmetric transformation in the alpha-hydroxylation of racemic malonates and its application to biologically active molecules.
2009
Two- and three-dimensional hydrated coordination polymers of diaqualanthanum(3+) ions with 2-hydroxypropanedioate, oxalate and acetate anions as bridging ligands.
2009 Apr
Oxidation of glycerol using gold-palladium alloy-supported nanocrystals.
2009 Jul 7
Bis(3-hydroxy-pyridinium) fumarate.
2009 Jun 24
Noninvasive determination of anaerobic threshold by monitoring the %SpO2 changes and respiratory gas exchange.
2009 Oct
Oxidation of glycerol by 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) in the presence of laccase.
2009 Oct
Impairment of aerobic glycolysis by inhibitors of lactic dehydrogenase hinders the growth of human hepatocellular carcinoma cell lines.
2010
Reactions of iodomalonic acid, diiodomalonic acid, and other organics in the Briggs-Rauscher oscillating system.
2010 Feb 25
Structural insights into the dual activities of the nerve agent degrading organophosphate anhydrolase/prolidase.
2010 Jan 26
Recognition of (2S)-aminomalonyl-acyl carrier protein (ACP) and (2R)-hydroxymalonyl-ACP by acyltransferases in zwittermicin A biosynthesis.
2010 May 4
Novel functionalized metal-organic framework based on unique hexagonal prismatic clusters.
2010 Oct 4
Rationale and design of the Exercise Intensity Trial (EXCITE): A randomized trial comparing the effects of moderate versus moderate to high-intensity aerobic training in women with operable breast cancer.
2010 Oct 6
Substance Class Chemical
Created
by admin
on Sat Dec 16 04:14:27 GMT 2023
Edited
by admin
on Sat Dec 16 04:14:27 GMT 2023
Record UNII
34T0025E0L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TARTRONIC ACID
MI  
Systematic Name English
.ALPHA.-HYDROXYMALONIC ACID
Common Name English
HYDROXYMALONIC ACID
Systematic Name English
NSC-36171
Code English
2-HYDROXYMALONIC ACID
Systematic Name English
TARTRONIC ACID [MI]
Common Name English
HYDROXYPROPANEDIOIC ACID
Systematic Name English
PROPANEDIOIC ACID, HYDROXY-
Common Name English
Code System Code Type Description
CAS
80-69-3
Created by admin on Sat Dec 16 04:14:27 GMT 2023 , Edited by admin on Sat Dec 16 04:14:27 GMT 2023
PRIMARY
CHEBI
16513
Created by admin on Sat Dec 16 04:14:27 GMT 2023 , Edited by admin on Sat Dec 16 04:14:27 GMT 2023
PRIMARY
EPA CompTox
DTXSID6075358
Created by admin on Sat Dec 16 04:14:27 GMT 2023 , Edited by admin on Sat Dec 16 04:14:27 GMT 2023
PRIMARY
MERCK INDEX
m10477
Created by admin on Sat Dec 16 04:14:27 GMT 2023 , Edited by admin on Sat Dec 16 04:14:27 GMT 2023
PRIMARY Merck Index
PUBCHEM
45
Created by admin on Sat Dec 16 04:14:27 GMT 2023 , Edited by admin on Sat Dec 16 04:14:27 GMT 2023
PRIMARY
ECHA (EC/EINECS)
201-301-1
Created by admin on Sat Dec 16 04:14:27 GMT 2023 , Edited by admin on Sat Dec 16 04:14:27 GMT 2023
PRIMARY
FDA UNII
34T0025E0L
Created by admin on Sat Dec 16 04:14:27 GMT 2023 , Edited by admin on Sat Dec 16 04:14:27 GMT 2023
PRIMARY
WIKIPEDIA
TARTRONIC ACID
Created by admin on Sat Dec 16 04:14:27 GMT 2023 , Edited by admin on Sat Dec 16 04:14:27 GMT 2023
PRIMARY
NSC
36171
Created by admin on Sat Dec 16 04:14:27 GMT 2023 , Edited by admin on Sat Dec 16 04:14:27 GMT 2023
PRIMARY