coumarin (Q111812)

image of molecular model or crystal lattice model

German Wikipedia

image

Coumarin sample.jpg
4,096 × 2,414; 421 KB

depicts

sample

0 references

Coumarin.png
1,437 × 1,000; 319 KB

depicts

ball-and-stick model

0 references

Coumarin spacefill.png
1,311 × 1,000; 288 KB

depicts

space-filling model

0 references

mass

146.037 dalton

1 reference

coumarin (English)

19 October 2016

C₉H₆O₂

1 reference

coumarin (English)

19 November 2016

C1=CC=C2C(=C1)C=CC(=O)O2

1 reference

coumarin (English)

19 November 2016

0.935 gram per cubic centimetre

1 reference

Russian Wikipedia

melting point

71 degree Celsius

1 reference

Russian Wikipedia

70 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

boiling point

301 degree Celsius

1 reference

safety classification and labelling

Russian Wikipedia

NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response

2

1

0

no value

1 reference

Recon 2.2: from reconstruction to model of human metabolism

2 references

A community-driven global reconstruction of human metabolism.

Dipteryx odorata

4 references

Occurrence of umbelliferone in the seeds of Dipteryx odorata (Aubl.) Willd

Determination of coumarin as an adulterant in vanilla flavoring products by high-performance liquid chromatography

Coumarin in vanilla extracts: Its detection and significance

Acaricidal activity of tonka bean extracts. Synthesis and structure-activity relationships of bioactive derivatives

Vanilla planifolia

2 references

Determination of Coumarin in Vanilla Flavorings by Quantitative High Performance Thin Layer Chromatography

Determination of coumarin as an adulterant in vanilla flavoring products by high-performance liquid chromatography

Lavandula latifolia

2 references

Constituents of the essential oil of Lavandula latifolia

Anti-inflammatory constituents of topically applied crude drugs. IV. Constituents and anti-inflammatory effect of Paraguayan crude drug "alhucema" (Lavandula latifolia Vill.).

Cinnamomum zeylanicum

1 reference

Volatile constituents of cinnamon (Cinnamomum zeylanicum) oils

Cinnamomum sieboldii

1 reference

Miscellaneous contributions to the essential oils of plants from various territories. XLVII. On the components of essential oils of Cinnamomum sieboldii Meisn

Thymus vulgaris

1 reference

Studies on the genotoxic properties of essential oils with Bacillus subtilis rec-assay and Salmonella/microsome reversion assay

Thapsia garganica

1 reference

Essential Oil of Thapsia garganica

Ageratum conyzoides

1 reference

Chemical composition of the essential oil ofAgeratum conyzoides L. (Asteraceae) from Réunion

Polygala senega

1 reference

Volatile compounds ofPolygala senega L. var.latifolia Torrey et Gray roots

Justicia pectoralis

3 references

Monoamine oxidase inhibitors in South American hallucinogenic plants Part 2: Constituents of orally-active Myristicaceous hallucinogens

Constituents of Justicia pectoralis Jacq. 2. Gas chromatography/mass spectrometry of simple coumarins, 3-phenylpropionic acids and their hydroxy and methoxy derivatives

Justicia pectoralis: A study of the basis for its use as a hallucinogenic snuff ingredient

Hydnellum suaveolens

1 reference

The Identity and Metabolic Fate of Volatiles Responsible for the Odor of Hydnellum suaveolens

Cullen drupaceum

1 reference

Phenolic components of the unsaponifiable fraction of the lipids of Psorlea drupaceae

Curcuma longa

1 reference

Characterization of powdered turmeric by liquid chromatography-mass spectrometry and gas chromatography-mass spectrometry

Fraxinus ornus

1 reference

Reverse-phase high pressure liquid chromatographic analysis of hydroxycoumarins in plant extracts. Quantitative determination of hydroxycoumarins inFraxinus ornus

Gliricidia sepium

1 reference

Allelopathic compounds in leaves ofGliricidia sepium (Jacq.) kunth ex walp. and its effect onSorghum vulgare L

Mikania glomerata

2 references

Development of a profitable procedure for the extraction of 2-H-1-benzopyran-2-one (coumarin) from Mikania glomerata

Seasonal Variation in Coumarin Content Mikania glomerata

Cinnamomum cassia

5 references

Determination of Cinnamomi Cortex by high-performance liquid chromatography

Determination of cinnamaldehyde, coumarin and cinnamyl alcohol in cinnamon and cassia by high-performance liquid chromatography

Monoamine oxidase inhibitors from Cinchonae Cortex

Chemical constituents from Cinnamomum cassia

Determination of cinnamaldehyde, coumarin and cinnamyl alcohol in cinnamon and cassia by high-performance liquid chromatography

Avena fatua

1 reference

Root exudates of wild oats: Allelopathic effect on spring wheat

Melilotus altus

3 references

Phytotoxic compounds from Melilotus alba (white sweet clover) and isolation and identification of two new flavonoids

Determination of coumarin in sweet clover herbage by a polarographic method

The biosynthesis of coumarin in Melilotus alba

Amburana cearensis

3 references

Bioactive phenolic glycosides from Amburana cearensis

Antinociceptive and antiedematogenic effects of the hydroalcoholic extract and coumarin from Torresea cearensis Fr. All

Amburosides C-H and 6-O-protocatechuoyl coumarin from Amburana cearensis

Scabiosa comosa

1 reference

Hentriacontane fromScabiosa comosa

Tetrapanax papyrifer

1 reference

Flavonoids and benzene derivatives from the flowers and fruit of Tetrapanax papyriferus

Artemisia reptans

1 reference

Sesquiterpene lactones and acetylenes from Artemisia reptans

Coriandrum sativum

1 reference

Antioxidant activity of methanolic extracts from three coriander (Coriandrum sativum L.) fruit varieties

Ageratum corymbosum

1 reference

Flavonoids from Ageratum corymbosum

Ajuga laxmannii

1 reference

Chemical Constituents of Ajuga parviflora

Althaea armeniaca

2 references

Coumarins of Althaea officinalis and A. armenica

Chromatographic Investigations of Phenolic Acids and Coumarins in the Leaves and Flowers of Some Species of the Genus Althaea

Althaea officinalis

1 reference

Coumarins of Althaea officinalis and A. armenica

Anthemis

1 reference

Antiproliferative effects of several compounds isolated from Amburana cearensis A. C. Smith

Artemisia annua

3 references

Terpenoids from the Seeds of Artemisia annua.

Terpenoids from the seeds of Artemisia annua

Two New Compounds from Artemisia annua

Artemisia anomala

1 reference

Chemical constituents of Artemisia lactiflora(Ⅱ)

Artemisia ludoviciana

1 reference

Seco-guaianolides and other constituents from Artemisia species

Artemisia rutifolia

1 reference

Seco-guaianolides and other constituents from Artemisia species

Artemisia vulgaris

1 reference

Coumarins of Artemesia vulgaris

Chromolaena tunariensis

1 reference

Ent-Clerodane derivatives from Chromolaena connivens

Cichorium intybus

1 reference

The role of sesquiterpene lactones and phenolics in the chemical defence of the chicory plant

Cryptocarya amygdalina

1 reference

The Constituents and Synthesis of Cryptamygin-A from the Stem Bark ofCryptocarya Amygadalina

Dendrobium chryseum

3 references

Chemical constituents of Dendrobium chrysotoxum

Chemical constituents of Dendrobium aurantiacum var. denneanum

Chemical constituents of Dendrobium crystallium

Halocnemum strobilaceum

1 reference

Coumarins from the aerial part of Halocnemum strobilaceum.

Haplophyllum buxbaumii

1 reference

Chemical Constituents of the Flora of Jordan, Part III. Mono-O-acetyl Diphyllin Apioside, a New Arylnaphthalene Lignan from Haplophyllum buxbaumii

Hevea brasiliensis

1 reference

Accumulation of scopoletin in Hevea brasiliensis infected by Microcyclus ulei (P. Henn.) V. ARX and evaluation of its fungitoxicity for three leaf pathogens of rubber tree

Hydrophyllum tenuipes

1 reference

BIOSYSTEMATICS OF THE GENUS HYDROPHYLLUM L. (HYDROPHYLLACEAE)

Iris

1 reference

Some antifungal components of diseased Blue Ribbon iris bulbs

Matricaria chamomilla

1 reference

Coumarins of Matricaria recutita

Q15561302

2 references

Antiulcerogenic activity of a crude hydroalcoholic extract and coumarin isolated from Mikania laevigata Schultz Bip.

New constituents from Mikania laevigata Shultz Bip. ex Baker

Mikania micrantha

1 reference

Germacra-1,10Z,4E-dien-12,8alpha-olides from Mikania micrantha.

Orchis militaris

1 reference

Additional Constituents of Orchis militaris

Ostericum grosseserratum

1 reference

Chemical Constituents from the Roots of <I>Vernicia fordii</I>

Phaseolus vulgaris

1 reference

Isolation of coumarin in snap beans and its effect on uredospore germination

Potentilla tormentilla

1 reference

Coumarins of the epigeal part ofPotentilla erecta

Prunus mahaleb

2 references

Coumarins inPrunus mahaleb and its herbivore, the small ermine mothYponomeuta mahalebellus.

Dihydrocoumarin and Certain Other Coumarins from Prunus mahaleb Seeds

Pteridium aquilinum

1 reference

Comparative dynamics of ptaquiloside and pterosin B in the two varieties (caudatum and arachnoideum) of neotropical Bracken Fern (Pteridium aquilinum L. Kuhn)

Rudbeckia laciniata

1 reference

Coumarin necrosis

Rudbeckia subtomentosa

1 reference

Ambrosanolides and other constituents of two rudbeckia species

Rudbeckia triloba

1 reference

Ambrosanolides and other constituents of two rudbeckia species

Seseli peucedanoides

1 reference

Coumarins ofSeseli peucedanoides

Simaba orinocensis

1 reference

Plant Anticancer Agents XXXV. Further Constituents of Simaba multiflora1,2

Tabernaemontana glandulosa

1 reference

Indole alkaloids fromTabernaemontana glandulosa

Ursinia abrotanifolia

1 reference

Sesquiterpene lactones and other constituents from Ursinia species

Ursinia dentata

1 reference

Sesquiterpene lactones and other constituents from Ursinia species

Ursinia trifida

1 reference

Sesquiterpene lactones and other constituents from Ursinia species

Yponomeuta mahalebellus

1 reference

Coumarins inPrunus mahaleb and its herbivore, the small ermine mothYponomeuta mahalebellus.

Achlys triphylla

1 reference

Note: The Occurrence of Coumarin in Achlys Triphylla.

Agrianthus pungens

1 reference

Guaianolides from Agrianthus pungens

Artemisia laciniata

1 reference

Seco-guaianolides and other constituents from Artemisia species

Artemisia lehmanniana

1 reference

9β-hydroxy-11β(H),13-dihyhdrosantamarine, a new eudesmanolide fromArtemisia leucotricha

Sweet Woodruff

1 reference

Über den Glucosid-Gehalt des Waldmeisters (Asperula odorata)

Cinnamomum macrostemon

1 reference

Chemical constituents from the twigs of Cinnamomum macrostemon

Cyperus rotundus

1 reference

Antiplatelet effects of Cyperus rotundus and its component (+)-nootkatone

Daphne mucronata

1 reference

Structural determination of daphnecin, a new coumarinolignan from Daphne mucronata.

Scapholeberis mucronata

1 reference

Structural determination of daphnecin, a new coumarinolignan from Daphne mucronata.

Eucalyptus viminalis

1 reference

Coumarins from Eucalyptus viminalis leaves

Eupatorium cannabinum

1 reference

Thymol, Benzofuranoid, and Phenylpropanoid Derivatives: Anti-inflammatory Constituents from Eupatorium cannabinum

Eupatorium japonicum

1 reference

Coumarin and Euponin, Two Inhibitors for Insect Development from Leaves ofEupatorium japonicum

Eupatorium fortunei

1 reference

New Acetophenone and Thymol Derivatives from Eupatorium stoechadosmum

Ixora coccinea

1 reference

Ixorapeptide I and ixorapeptide II, bioactive peptides isolated from Ixora coccinea

Nidorella anomala

1 reference

Ent-beyer-15-ene derivatives from Nidorella anomala

Nidorella hottentotica

1 reference

Unusual diterpenes and sesquiterpene xylosides from Nidorella hottentotica

Potentilla erecta

1 reference

Coumarins of the epigeal part ofPotentilla erecta

Rhododendron formosanum

1 reference

Two isomeric epoxysitosterols from Rhododendron formosanum: 1H and 13C NMR chemical shift assignments

Sarcandra glabra

1 reference

Cycloeudesmanolides from Sarcandra glabra

Sempervivum ruthenicum

1 reference

Phenolic compounds of Sempervivum ruthenicum

Uvaria afzelii

1 reference

New flavonoid and coumarin derivatives of Uvaria afzelii

Viburnum cylindricum

1 reference

Seven New Phenolic Glucosides fromViburnum cylindricum

Rutaceae

1 reference

Strategies for the isolation and identification of trypanocidal compounds from the Rutales

Pterocaulon

1 reference

Selective cytotoxicity and apoptosis induction in glioma cell lines by 5-oxygenated-6,7-methylenedioxycoumarins from Pterocaulon species

Streptomyces

1 reference

Defense responses in plants of Eucalyptus elicited by Streptomyces and challenged with Botrytis cinerea.

Dendrobium aurantiacum

1 reference

Chemical constituents of Dendrobium aurantiacum var. denneanum

Nama johnstonii

1 reference

Shifts In Panama The Military Steps Ahead

Yponomeuta mahalebella

1 reference

Coumarins inPrunus mahaleb and its herbivore, the small ermine mothYponomeuta mahalebellus.

Cinnamomum insulari-montanum

1 reference

Chemical constituents from the stems of Cinnamomum insulari-montanum

Melilotus siculus

1 reference

Flavonoids and coumarins of Anthemis pseudocotiola

Prunus persica

1 reference

Coumarins of Prunella vulgaris

Dianthus superbus

1 reference

Activation of apoptosis by ethyl acetate fraction of ethanol extract of Dianthus superbus in HepG2 cell line

Rudbeckia fulgida var. speciosa

1 reference

1 reference

Coumarins ofZosima korovinii

Caragana frutex

1 reference

Coumarins of the epigeal part ofCaragana frutex

Cnidium monnieri

1 reference

Coumarins from the fruits of Cnidium monnieri

Perezia hebeclada

1 reference

A new coumarin fromPerezia hebeclada

Skimmia laureola

1 reference

Chromones and coumarins from Skimmia laureola

Phebalium megaphyllum

1 reference

Coumarins from Phebalium tuberculosum ssp. megaphyllum and Phebalium filifolium

Centaurea besseriana

1 reference

Coumarins of plants of the genus Centaurea

Acourtia cordata

1 reference

A new coumarin fromPerezia hebeclada

Mantisalca salmantica

1 reference

Coumarins of plants of the genus Centaurea

Polygonum weyrichii

1 reference

Coumarins and flavonoids of some species ofPolygonum

Caenorhabditis elegans

1 reference

Modeling Meets Metabolomics-The WormJam Consensus Model as Basis for Metabolic Studies in the Model Organism

pomelo

1 reference

Alkaloids and coumarins of Citrus grandis

Citrus × paradisi

1 reference

Alkaloids and coumarins of Citrus grandis

Citrus grandis

1 reference

Alkaloids and coumarins of Citrus grandis

Medicago sativa

1 reference

Biological Activity and Quantification of Suspected Allelochemicals from Alfalfa Plant Parts

Salvia officinalis

1 reference

Total Phenolics, Flavonoids, and Antioxidant Activity of Sage (Salvia officinalis L.) Plants as Affected by Different Drying Methods

Morus alba

1 reference

The novel contributors of anti-diabetic potential in mulberry polyphenols revealed by UHPLC-HR-ESI-TOF-MS/MS.

Oryza sativa

1 reference

Assessment of nutritional value and quantitative analysis of bioactive phytochemicals through targeted LC-MS/MS method in selected scented and pigmented rice varietals

Clausena excavata

1 reference

Chemodiversity of Clausena excavata (Rutaceae) and related species: Coumarins and carbazoles

Calophyllum brasiliense

1 reference

Antiproliferative, cytotoxic and antitumour activity of coumarins isolated from Calophyllum brasiliense.

Cinnamomum yabunikkei

1 reference

Chemical constituents from the stems of Cinnamomum insulari-montanum

Cinnamon

1 reference

Volatile constituents of cinnamon (Cinnamomum zeylanicum) oils

Cinnamomum burmanni

6 references

Chemical constituents from the twigs of Cinnamomum macrostemon

Determination of Cinnamomi Cortex by high-performance liquid chromatography

Determination of cinnamaldehyde, coumarin and cinnamyl alcohol in cinnamon and cassia by high-performance liquid chromatography

Monoamine oxidase inhibitors from Cinchonae Cortex

Chemical constituents from Cinnamomum cassia

Determination of cinnamaldehyde, coumarin and cinnamyl alcohol in cinnamon and cassia by high-performance liquid chromatography

Melilotus messanensis

1 reference

Flavonoids and coumarins of Anthemis pseudocotiola

Chamomilla recutita

1 reference

Coumarins of Matricaria recutita

Hydrophyllum virginianum

1 reference

BIOSYSTEMATICS OF THE GENUS HYDROPHYLLUM L. (HYDROPHYLLACEAE)

Melilotus officinalis

6 references

Extraction of coumarins from plant material (Leguminosae)

Effects of Melilotus officinalis on acute inflammation

Determination of coumarin in sweet clover herbage by a polarographic method

Ueber das Cumarin aus dem Steinklee (Melilotus officinalis)

Phytotoxic compounds from Melilotus alba (white sweet clover) and isolation and identification of two new flavonoids

The biosynthesis of coumarin in Melilotus alba

Lavandula angustifolia

1 reference

Pigment formation by callus of Lavandula angustifolia

Eupatorium formosanum

1 reference

Thymol, Benzofuranoid, and Phenylpropanoid Derivatives: Anti-inflammatory Constituents from Eupatorium cannabinum

Alyxia reinwardtii

1 reference

Three monohydroxycoumarins from Alyxia lucida

Senecio gilliesianus

1 reference

1-Hydroxyplatyphyllide, a norsesquiterpene lactone from Senecio gilliesiano

Petchia erythrocarpa

1 reference

Three monohydroxycoumarins from Alyxia lucida

Matsutake

1 reference

Volatile flavor compounds of Matsutake-Tricholomam atsutake (Ito et Imai) Sing.

physically interacts with

taste receptor type 2

subject has role

agonist

1 reference

The Molecular Receptive Ranges of Human TAS2R Bitter Taste Receptors

described by source

Armenian Soviet Encyclopedia, vol. 6

page(s)

11

0 references

1 reference

0 references

0 references

0 references

Coumarin

0 references

Identifiers

National Library of Latvia ID

0 references

0 references

InChI=1S/C9H6O2/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-6H

1 reference

coumarin (English)

19 November 2016

2 references

coumarin (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

91-64-5

2 references

coumarin (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=91-64-5

9 April 2021

1 reference

Coumarin (English)

19 November 2016

2 references

English

title

coumarin (English)

19 November 2016

Reaxys registry number

383644

1 reference

coumarin (English)

19 October 2016

165222

0 references

ChEBI ID

28794

mapping relation type

3 references

COUMARIN (English)

19 November 2016

ChEBI release 2019-10-02

International Chemical Identifier

InChI

InChI=1S/C9H6O2/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-6H

1 reference

COUMARIN (English)

19 November 2016

2 references

inferred from InChIKey

Cambridge Structural Database

1 reference

1 reference

10 January 2023

1 reference

Cambridge Structural Database

MSBNK-Fac_Eng_Univ_Tokyo-JP001132

10 January 2023

based on heuristic

InChIKey match

MassBank accession ID

SM817901

0 references

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP009576

0 references

MSBNK-Fiocruz-FIO00033

0 references

MSBNK-Fiocruz-FIO00034

0 references

MSBNK-Fiocruz-FIO00035

0 references

MSBNK-Fiocruz-FIO00036

0 references

MSBNK-Fiocruz-FIO00037

0 references

MSBNK-Washington_State_Univ-BML01352

0 references

MSBNK-Washington_State_Univ-BML01359

0 references

MSBNK-Washington_State_Univ-BML01366

0 references

MSBNK-Washington_State_Univ-BML80985

0 references

MSBNK-Washington_State_Univ-BML80987

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP007406

0 references

MSBNK-IPB_Halle-PB004701

0 references

MSBNK-IPB_Halle-PB004702

0 references

MSBNK-IPB_Halle-PB004703

0 references

SPLASH

splash10-014i-7900000000-25bab36f91f71ac65817

0 references

splash10-02tj-9600000000-4a54f8d648a87a9c5811

0 references

splash10-0002-0900000000-c06b97954c5a847401e8

0 references

splash10-0002-1900000000-6f05165347e6221503b0

0 references

splash10-0f6x-8900000000-6e9532ad6b20b76b3d4b

0 references

splash10-0006-9300000000-3f95abb339f5c1aea790

0 references

splash10-0006-9200000000-c404268b480236aaf197

0 references

splash10-0f6x-9500000000-da852779b618f093b767

0 references

splash10-0006-9300000000-c29bd55b8ca9510aec2f

0 references

splash10-0006-9100000000-161d49edf4310e8a785c

0 references

splash10-0002-0900000000-3777f28f5438e1f09160

0 references

splash10-0udi-0900000000-bfe432f57faff8d62318

0 references

splash10-0089-0000800900-d301ec3931fa0374d57a

0 references

splash10-0002-0900000000-d77a33dd1d897b45de4d

0 references

splash10-0002-0900000000-8600b62e04fce45b48b4

0 references

splash10-000i-9200000000-bbe6d1ada55f447ac2cf

0 references

splash10-0690-7900000000-8f6a314f888a9067271c

0 references

splash10-001i-0900000000-c31c44b07b1f139cd7bc

0 references

splash10-015a-0900000100-6ae81e23a1a6770a9f59

0 references

splash10-0002-0900000000-0ac49ca1676aa2241ed9

0 references

splash10-014v-6900000000-3e901733dc003512f338

0 references

splash10-00kb-9700000000-7a649c1e257a7ad17b9d

0 references

splash10-0002-0900000000-6ef9288c71771dd56774

0 references

splash10-0006-9100000000-93154d9b40c4d0fdd1ae

0 references

splash10-014i-9000000000-72ec22913d1d574be75b

0 references

NMRShiftDB structure ID

10008786

1 reference

0 references

0 references

GN4200000

1 reference

Spanish Wikipedia

ZVG number

490110

1 reference

Hazardous Substances Data Bank

1 reference

28 October 2019

COUMARIN (English)

10 May 2021

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

0 references

1 reference

English

title

coumarin (English)

ECHA Substance Infocard ID

19 November 2016

100.001.897

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

Coumarin (English)

CAS no.: 91-64-5 (English)

1 reference

28 December 2019

COUMARIN (English)

CAS no.: 91-64-5 (English)

PesticideInfo chemical ID

0 references

1 reference

1 reference

coumarin (English)

19 November 2016

1 reference

Human Metabolome Database ID

HMDB0001218

2 references

based on heuristic

inferred from InChIKey

3 references

coumarin (English)

19 October 2016

inferred from InChIKey

2 references

English

title

coumarin (English)

19 November 2016

0 references

1 reference

1 reference

Modeling Meets Metabolomics-The WormJam Consensus Model as Basis for Metabolic Studies in the Model Organism

coumarin (English)

19 October 2016

1 reference

IEDB Epitope ID

114082

1 reference

Immune Epitope Database and Analysis Resource

1 January 2022

0 references

Brockhaus Enzyklopädie online ID

0 references

1 reference

California Proposition 65 list of chemicals

https://oehha.ca.gov/chemicals/coumarin

12 December 2019

reference URL

1 reference

6 April 2020

0 references

Encyclopædia Britannica Online ID

science/coumarin

subject named as

coumarin

0 references

1 reference

28 October 2013

Gran Enciclopèdia Catalana ID

cumarina

0 references

Gran Enciclopèdia Catalana ID (former scheme)

0173556

0 references

0095463

0 references

Great Russian Encyclopedia Online ID (old version)

2121509

subject named as

КУМАРИН

reason for deprecated rank

redirected to GRE portal

0 references

Great Russian Encyclopedia portal ID

kumarin-aba67f

0 references

HCIS ID

5442

0 references

JSTOR topic ID (archived)

coumarins

0 references

Microsoft Academic ID

2781338262

0 references

OmegaWiki Defined Meaning

0 references

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

archive URL

https://web.archive.org/web/20220125070108/https://docs.openalex.org/download-snapshot/snapshot-data-format

25 January 2022

1 reference

2PMJ (English)

19 October 2016

1 reference

3L68 (English)

19 October 2016

1 reference

3CRB (English)

19 October 2016

1 reference

2H90 (English)

19 October 2016

1 reference

3L5M (English)

19 October 2016

1 reference

3L66 (English)

19 October 2016

1 reference

4UTI (English)

19 October 2016

1 reference

4UTL (English)

19 October 2016

1 reference

1Z10 (English)

19 October 2016

1 reference

2PWB (English)

19 October 2016

1 reference

1 reference

German Wikipedia

Store norske leksikon ID

0 references

kumariinit

kumariner

coumarins

1 reference

YSO-Wikidata mapping project