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Details

Stereochemistry ACHIRAL
Molecular Formula C10H8O3
Molecular Weight 176.1687
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 7-METHOXYCOUMARIN

SMILES

COC1=CC=C2C=CC(=O)OC2=C1

InChI

InChIKey=LIIALPBMIOVAHH-UHFFFAOYSA-N
InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3

HIDE SMILES / InChI

Molecular Formula C10H8O3
Molecular Weight 176.1687
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Detection and functional characterization of a 215 amino acid N-terminal extension in the Xanthomonas type III effector XopD.
2010-12-22
Computational approach to characterization of human liver drug-metabolizing enzymes.
2010-10-09
Array comparative genomic hybridization analysis of Trichoderma reesei strains with enhanced cellulase production properties.
2010-07-19
The coumarin herniarin as a sensitizer in German chamomile [Chamomilla recutita (L.) Rauschert, Compositae].
2010-06
Leucine aminopeptidase, beta-glucosidase and alkaline phosphatase activity rates and their significance in nutrient cycles in some coastal Mediterranean sites.
2010-03-29
Structure and kinetic investigation of Streptococcus pyogenes family GH38 alpha-mannosidase.
2010-02-03
Versatile dual reporter gene systems for investigating stop codon readthrough in plants.
2009-10-09
Hypoglycemic activity of constituents from Astianthus viminalis in normal and streptozotocin-induced diabetic mice.
2009-10
Lavender as a source of novel plant compounds for the development of a natural herbicide.
2009-09
Anti-collagenase, anti-elastase and anti-oxidant activities of extracts from 21 plants.
2009-08-04
Circadian rhythm of Z- and E-2-beta-D: -glucopyranosyloxy-4-methoxy cinnamic acids and herniarin in leaves of Matricaria chamomilla.
2009-07
Antiamoebic coumarins from the root bark of Adina cordifolia and their new thiosemicarbazone derivatives.
2009-05
Salicylic acid-induced changes to growth and phenolic metabolism in Matricaria chamomilla plants.
2009-01
Simultaneous determination of 13 bioactive compounds in Herba Artemisiae Scopariae (Yin Chen) from different harvest seasons by HPLC-DAD.
2008-08-05
Simultaneous determination of 6-methylcoumarin and 7-methoxycoumarin in cosmetics using three-dimensional excitation-emission matrix fluorescence coupled with second-order calibration methods.
2008-06-15
Multi-substrate flavonol O-glucosyltransferases from strawberry (Fragaria x ananassa) achene and receptacle.
2008
Constituents, biological activities and quality control parameters of the crude extract and essential oil from Arracacia tolucensis var. multifida.
2007-08-15
Antimicrobial activity of the methanolic extracts and compounds from Treculia obovoidea (Moraceae).
2007-07-25
Capillary electrochromatography of selected phenolic compounds of Chamomilla recutita.
2007-06-22
Structure activity studies with xenobiotic substrates using carboxylesterases isolated from Arabidopsis thaliana.
2007-03
Quantification of spiroether isomers and herniarin of different parts of Matricaria matricarioides and flowers of Chamaemelum nobile.
2007-01-31
[Studies on chemical constituents in herb from Artemisia rupestris].
2006-11
Inhibition of respiratory burst in human neutrophils and lipoxygenase enzyme by compounds from Haloxylon griffithii.
2006-10
Simultaneous determination of urinary metabolites of methoxypsoralens in human and Umbelliferae medicines by high-performance liquid chromatography.
2006-09
Synthesis of chemical probes to map sulfenic acid modifications on proteins.
2005-11-17
The chemical constituents of Ligularia pleurocaulis.
2005-06
Quantitative changes of secondary metabolites of Matricaria chamomilla by abiotic stress.
2005-04-09
Stereospecific high-performance liquid chromatographic analysis of hesperetin in biological matrices.
2005-03-09
Solid-phase extraction of esculetin from the ash bark of Chinese traditional medicine by using molecularly imprinted polymers.
2005-01-07
Gender dimorphism and altitudinal variation of secondary compounds in leaves of the gynodioecious shrub Daphne laureola.
2005-01
Coumarin and flavone derivatives from estragon and thyme as inhibitors of chemical mediator release from RBL-2H3 Cells.
2005-01
A rapid and highly sensitive method for measuring enzyme activities in single mycorrhizal tips using 4-methylumbelliferone-labelled fluorogenic substrates in a microplate system.
2004-08
Antifungal constituents of Melicope borbonica.
2004-07
Constituents of Peucedanum zenkeri seeds and their antimicrobial effects.
2003-08
Atom economy. Palladium-catalyzed formation of coumarins by addition of phenols and alkynoates via a net C-H insertion.
2003-04-16
Natural fungicides from Ruta graveolens L. leaves, including a new quinolone alkaloid.
2003-02-12
An extract of Tagetes lucida and its phenolic constituents as antioxidants.
2002-12
5-hydroxyramulosin, a new natural product produced by Phoma tropica, a marine-derived fungus isolated from the alga Fucus spiralis.
2002-11
Development of an enzyme assay for rapid assessment of Escherichia coli in seawaters.
2002
Use of the tape stripping technique for directly quantifying esterase activities in human stratum corneum.
2001-03
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:36:58 GMT 2025
Edited
by admin
on Mon Mar 31 19:36:58 GMT 2025
Record UNII
DGK72G008A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-404559
Preferred Name English
7-METHOXYCOUMARIN
Systematic Name English
AYAPANIN
Common Name English
METHYLUMBELLIFERONE
Common Name English
METHOXYCOUMARIN, 7-
Systematic Name English
HERNIARIN
Common Name English
7-METHOXYCOUMARIN (CONSTITUENT OF CHAMOMILE) [DSC]
Common Name English
2H-1-BENZOPYRAN-2-ONE, 7-METHOXY-
Systematic Name English
Code System Code Type Description
PUBCHEM
10748
Created by admin on Mon Mar 31 19:36:58 GMT 2025 , Edited by admin on Mon Mar 31 19:36:58 GMT 2025
PRIMARY
EPA CompTox
DTXSID5060196
Created by admin on Mon Mar 31 19:36:58 GMT 2025 , Edited by admin on Mon Mar 31 19:36:58 GMT 2025
PRIMARY
FDA UNII
DGK72G008A
Created by admin on Mon Mar 31 19:36:58 GMT 2025 , Edited by admin on Mon Mar 31 19:36:58 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-513-3
Created by admin on Mon Mar 31 19:36:58 GMT 2025 , Edited by admin on Mon Mar 31 19:36:58 GMT 2025
PRIMARY
CAS
531-59-9
Created by admin on Mon Mar 31 19:36:58 GMT 2025 , Edited by admin on Mon Mar 31 19:36:58 GMT 2025
PRIMARY
CHEBI
28184
Created by admin on Mon Mar 31 19:36:58 GMT 2025 , Edited by admin on Mon Mar 31 19:36:58 GMT 2025
PRIMARY
NSC
404559
Created by admin on Mon Mar 31 19:36:58 GMT 2025 , Edited by admin on Mon Mar 31 19:36:58 GMT 2025
PRIMARY
CHEBI
5679
Created by admin on Mon Mar 31 19:36:58 GMT 2025 , Edited by admin on Mon Mar 31 19:36:58 GMT 2025
PRIMARY
WIKIPEDIA
Herniarin
Created by admin on Mon Mar 31 19:36:58 GMT 2025 , Edited by admin on Mon Mar 31 19:36:58 GMT 2025
PRIMARY
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