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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
Generation of hydroxyl radicals by the antiviral compound phosphonoformic acid (foscarnet).
2001 Jul
Synthesis and characterization of a binuclear coumarin-3-carboxylate copper(II) complex.
2001 Mar
Measurement of ascorbic acid (vitamin C) induced hydroxyl radical generation in household drinking water.
2002 Dec
[Generation of hydroxyl radicals and other redox active compounds in the sea water exposed to heat].
2002 Sep-Oct
[Heat-induced activation of reducing properties of of sea water].
2003 Nov-Dec
2-Amino-1,3-benzothiazole-ethyl coumarin-3-carboxylate (1/1).
2003 Oct
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 Jan 6
New Samarium(III), Gadolinium(III), and Dysprosium(III) Complexes of Coumarin-3-Carboxylic Acid as Antiproliferative Agents.
2007
Near infrared multiphoton-induced generation and detection of hydroxyl radicals in a biochemical system.
2007 Aug 15
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 Dec 10
Anticancer Activity of Ag(I) N-Heterocyclic Carbene Complexes Derived from 4,5-Dichloro-1H-Imidazole.
2008
Effect of amino acids on X-ray-induced hydrogen peroxide and hydroxyl radical formation in water and 8-oxoguanine in DNA.
2008 Apr
Synthesis and application of molecular probe for detection of hydroxyl radicals produced by Na(125)I and gamma-rays in aqueous solution.
2008 Dec
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 Dec
Six naphthylisoquinoline alkaloids and a related benzopyranone from a Congolese Ancistrocladus species related to Ancistrocladus congolensis.
2008 Feb
[Formation of hydrogen peroxide and hydroxyl radicals in aqueous solutions of L-amino acids by the action of X-rays and heat].
2008 Jan-Feb
Diaqua-bis-(2-oxo-2H-chromene-3-carboxyl-ato-κO,O)cadmium.
2010 Dec 24
Synthesis and biological evaluation of coumarin derivatives as inhibitors of Mycobacterium bovis (BCG).
2012 Dec
Substance Class Chemical
Created
by admin
on Sat Dec 16 04:28:55 GMT 2023
Edited
by admin
on Sat Dec 16 04:28:55 GMT 2023
Record UNII
V85UOV8788
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
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
G 1 (RODENTICIDE)
Brand Name English
NSC-53239
Code English
Code System Code Type Description
CAS
531-81-7
Created by admin on Sat Dec 16 04:28:55 GMT 2023 , Edited by admin on Sat Dec 16 04:28:55 GMT 2023
PRIMARY
EPA CompTox
DTXSID70201183
Created by admin on Sat Dec 16 04:28:55 GMT 2023 , Edited by admin on Sat Dec 16 04:28:55 GMT 2023
PRIMARY
PUBCHEM
10752
Created by admin on Sat Dec 16 04:28:55 GMT 2023 , Edited by admin on Sat Dec 16 04:28:55 GMT 2023
PRIMARY
MERCK INDEX
m3821
Created by admin on Sat Dec 16 04:28:55 GMT 2023 , Edited by admin on Sat Dec 16 04:28:55 GMT 2023
PRIMARY Merck Index
FDA UNII
V85UOV8788
Created by admin on Sat Dec 16 04:28:55 GMT 2023 , Edited by admin on Sat Dec 16 04:28:55 GMT 2023
PRIMARY
NSC
14797
Created by admin on Sat Dec 16 04:28:55 GMT 2023 , Edited by admin on Sat Dec 16 04:28:55 GMT 2023
PRIMARY
NSC
53239
Created by admin on Sat Dec 16 04:28:55 GMT 2023 , Edited by admin on Sat Dec 16 04:28:55 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-518-0
Created by admin on Sat Dec 16 04:28:55 GMT 2023 , Edited by admin on Sat Dec 16 04:28:55 GMT 2023
PRIMARY