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Details

Stereochemistry ACHIRAL
Molecular Formula C10H6O4
Molecular Weight 190.1522
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of COUMARIN-3-CARBOXYLIC ACID

SMILES

OC(=O)C1=CC2=C(OC1=O)C=CC=C2

InChI

InChIKey=ACMLKANOGIVEPB-UHFFFAOYSA-N
InChI=1S/C10H6O4/c11-9(12)7-5-6-3-1-2-4-8(6)14-10(7)13/h1-5H,(H,11,12)

HIDE SMILES / InChI

Molecular Formula C10H6O4
Molecular Weight 190.1522
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis and biological evaluation of coumarin derivatives as inhibitors of Mycobacterium bovis (BCG).
2012-12
Diaqua-bis-(2-oxo-2H-chromene-3-carboxyl-ato-κO,O)cadmium.
2010-12-24
Diaqua-bis-(2-oxo-2H-chromene-3-carboxyl-ato)zinc(II).
2010-12-11
Structural and functional characterization of a promiscuous feruloyl esterase (Est1E) from the rumen bacterium Butyrivibrio proteoclasticus.
2010-05-01
Cinnamyl 2-oxo-2H-chromene-3-carboxyl-ate.
2009-11-04
Synergistic effects of metal ion and the pre-senile cataract-causing G98R alphaA-crystallin: self-aggregation propensities and chaperone activity.
2009-10-16
Peculiarities of the antioxidant and radioprotective effects of hydrated C60 fullerene nanostuctures in vitro and in vivo.
2009-09-15
Menthyl 2-oxo-2H-chromene-3-carboxyl-ate.
2009-09-12
Trans-cinnamic acid and coumarin-3-carboxylic acid: experimental charge-density studies to shed light on [2 + 2] cycloaddition reactions.
2009-04
Efficient shRNA delivery into B and T lymphoma cells using lentiviral vector-mediated transfer.
2009-03
Synthesis and application of molecular probe for detection of hydroxyl radicals produced by Na(125)I and gamma-rays in aqueous solution.
2008-12
6-Substituted 2-oxo-2H-1-benzopyran-3-carboxylic acid derivatives in a new approach of the treatment of cancer cell invasion and metastasis.
2008-12
[Formation of hydrogen peroxide and hydroxyl radicals in aqueous solutions of L-amino acids by the action of X-rays and heat].
2008-05-21
Effect of amino acids on X-ray-induced hydrogen peroxide and hydroxyl radical formation in water and 8-oxoguanine in DNA.
2008-04
Six naphthylisoquinoline alkaloids and a related benzopyranone from a Congolese Ancistrocladus species related to Ancistrocladus congolensis.
2008-02
Anticancer Activity of Ag(I) N-Heterocyclic Carbene Complexes Derived from 4,5-Dichloro-1H-Imidazole.
2008
Theoretical study of metal-ligand interaction in Sm(III), Eu(III), and Tb(III) complexes of coumarin-3-carboxylic acid in the gas phase and solution.
2007-12-10
Biological activity of 3-formylchromones and related compounds.
2007-11-21
Near infrared multiphoton-induced generation and detection of hydroxyl radicals in a biochemical system.
2007-08-15
Asymmetric total synthesis of (-)-Linderol A.
2007-07-20
A study of the role of apoptotic cell death and cell cycle events mediating the mechanism of action of 6-hydroxycoumarin-3-carboxylatosilver in human malignant hepatic cells.
2007-05-18
In vitro anti-tumour and cyto-selective effects of coumarin-3-carboxylic acid and three of its hydroxylated derivatives, along with their silver-based complexes, using human epithelial carcinoma cell lines.
2007-04-18
[Guanosine and inosine as natural geneprotectors for mice blood cells exposed to X-rays].
2007-02-28
New Samarium(III), Gadolinium(III), and Dysprosium(III) Complexes of Coumarin-3-Carboxylic Acid as Antiproliferative Agents.
2007
Guanosine and inosine as natural antioxidants and radioprotectors for mice exposed to lethal doses of gamma-radiation.
2006-06-17
Guanosine and inosine display antioxidant activity, protect DNA in vitro from oxidative damage induced by reactive oxygen species, and serve as radioprotectors in mice.
2006-05
(Sub)-picosecond spectral evolution of fluorescence in photoactive proteins studied with a synchroscan streak camera system.
2006-04-15
Diels-Alder reactions of 3-substituted coumarins in water and under high-pressure condition. An uncatalyzed route to tetrahydro-6H-benzo[c]chromen-6-ones.
2006-01-06
Effects of iron on Vitamin C/copper-induced hydroxyl radical generation in bicarbonate-rich water.
2005-05
Inhibition of monoamine oxidases by coumarin-3-acyl derivatives: biological activity and computational study.
2004-07-16
Glucuronidation of carboxylic acid containing compounds by UDP-glucuronosyltransferase isoforms.
2004-04-15
[Heat-induced activation of reducing properties of of sea water].
2004-01-13
Fungal modification of the hydroxyl radical detector coumarin-3-carboxylic acid.
2003-11-01
2-Amino-1,3-benzothiazole-ethyl coumarin-3-carboxylate (1/1).
2003-10
Superoxide dismutase: the balance between prevention and induction of oxidative damage.
2003-03-06
Measurement of ascorbic acid (vitamin C) induced hydroxyl radical generation in household drinking water.
2002-12
[Generation of hydroxyl radicals and other redox active compounds in the sea water exposed to heat].
2002-10-26
Detection of hydroxyl radicals produced by wood-decomposing fungi.
2002-04-01
Generation of hydroxyl radicals by the antiviral compound phosphonoformic acid (foscarnet).
2001-07
Synthesis and characterization of a binuclear coumarin-3-carboxylate copper(II) complex.
2001-03
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:22:11 GMT 2025
Edited
by admin
on Mon Mar 31 21:22:11 GMT 2025
Record UNII
V85UOV8788
Record Status Validated (UNII)
Record Version
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Name Type Language
G 1 (RODENTICIDE)
Preferred Name English
COUMARIN-3-CARBOXYLIC ACID
MI  
Systematic Name English
1,2-BENZOPYRAN-3-CARBOXYLIC ACID, 2-KETO-
Common Name English
COUMARIN-3-CARBOXYLIC ACID [MI]
Common Name English
2H-1-BENZOPYRAN-2-ONE-3-CARBOXYLIC ACID
Common Name English
3-CARBOXYLCOUMARIN
Common Name English
NSC-14797
Code English
3-CARBOXYCOUMARIN
Systematic Name English
2-OXO-2H-CHROMENE-3-CARBOXYLIC ACID
Systematic Name English
2-OXO-2H-1-BENZOPYRAN-3-CARBOXYLIC ACID
Systematic Name English
NSC-53239
Code English
Code System Code Type Description
CAS
531-81-7
Created by admin on Mon Mar 31 21:22:11 GMT 2025 , Edited by admin on Mon Mar 31 21:22:11 GMT 2025
PRIMARY
EPA CompTox
DTXSID70201183
Created by admin on Mon Mar 31 21:22:11 GMT 2025 , Edited by admin on Mon Mar 31 21:22:11 GMT 2025
PRIMARY
PUBCHEM
10752
Created by admin on Mon Mar 31 21:22:11 GMT 2025 , Edited by admin on Mon Mar 31 21:22:11 GMT 2025
PRIMARY
MERCK INDEX
m3821
Created by admin on Mon Mar 31 21:22:11 GMT 2025 , Edited by admin on Mon Mar 31 21:22:11 GMT 2025
PRIMARY Merck Index
FDA UNII
V85UOV8788
Created by admin on Mon Mar 31 21:22:11 GMT 2025 , Edited by admin on Mon Mar 31 21:22:11 GMT 2025
PRIMARY
NSC
14797
Created by admin on Mon Mar 31 21:22:11 GMT 2025 , Edited by admin on Mon Mar 31 21:22:11 GMT 2025
PRIMARY
NSC
53239
Created by admin on Mon Mar 31 21:22:11 GMT 2025 , Edited by admin on Mon Mar 31 21:22:11 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-518-0
Created by admin on Mon Mar 31 21:22:11 GMT 2025 , Edited by admin on Mon Mar 31 21:22:11 GMT 2025
PRIMARY