adenosine (Q190012)

reactant

1 reference

1 reference

adenosine metabolic process

participant

1 reference

adenosine biosynthetic process

product

1 reference

1 reference

G protein-coupled adenosine receptor activity

reactant

1 reference

adenosine deaminase activity

1 reference

adenosine kinase activity

1 reference

adenosylhomocysteinase activity

1 reference

nucleoside oxidase (hydrogen peroxide-forming) activity

1 reference

adenosine nucleosidase activity

1 reference

AMP-thymidine kinase activity

1 reference

http://geneontology.org/external2go/rhea2go

1 February 2021

0 references

Adenosin.svg
200 × 169; 7 KB

1 reference

imported from Wikimedia project

German Wikipedia

mass

267.097 dalton

1 reference

adenosine (English)

19 October 2016

C₁₀H₁₃N₅O₄

1 reference

adenosine (English)

19 November 2016

C1=NC2=C(C(=N1)N)N=CN2C3C(C(C(O3)CO)O)O

1 reference

adenosine (English)

19 November 2016

C1=NC2=C(C(=N1)N)N=CN2[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O

1 reference

adenosine (English)

19 November 2016

235.5 degree Celsius

1 reference

CRC Handbook of Chemistry and Physics (97th edition)

3-10

235 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

solubility

5.1 gram per kilogram

25 degree Celsius

1 reference

CRC Handbook of Chemistry and Physics (97th edition)

5-139

3.6

25 degree Celsius

1

1 reference

CRC Handbook of Chemistry and Physics (97th edition)

5-88

12.4

temperature

25 degree Celsius

series ordinal

2

1 reference

CRC Handbook of Chemistry and Physics (97th edition)

parenteral route of administration

5-88

defined daily dose

15 milligram

route of administration

1 reference

Anatomical Therapeutic Chemical Classification System

1 reference

14 February 2018

1 reference

14 February 2018

World Health Organisation international non-proprietary name

Adenosine (English)

1 reference

Recon 2.2: from reconstruction to model of human metabolism

Adenosine (English)

19 January 2016

2 references

A community-driven global reconstruction of human metabolism.

Cynomorium songaricum

2 references

Inhibitory effects of ursolic acid derivatives from Cynomorium songaricum, and related triterpenes on human immunodeficiency viral protease

Inhibitory effects of constituents from Cynomorium songaricum and related triterpene derivatives on HIV-1 protease

Acanthus ebracteatus

1 reference

Megastigmane, aliphatic alcohol and benzoxazinoid glycosides from Acanthus ebracteatus

Acanthus ilicifolius

2 references

Phenylethanoid and aliphatic alcohol glycosides from Acanthus ilicifolius

Benzoxazinoid glucosides from Acanthus ilicifolius

Adiantum lunulatum

1 reference

A new triterpenoid from the fern Adiantum lunulatum and evaluation of antibacterial activity

Allium tuberosum

1 reference

A steroidal saponin from the seeds of Allium tuberosum

Atractylodes lancea

1 reference

Glycosides of Atractylodes ovata

Capparis flavicans

1 reference

Antiestrogenic constituents of the Thai medicinal plants Capparis flavicans and Vitex glabrata

Cassytha filiformis

1 reference

Vasorelaxing alkaloids and flavonoids from Cassytha filiformis

Codonopsis pilosula

1 reference

Phenolic glycosides and pyrrolidine alkaloids from Codonopsis tangshen

Crocus sativus

5 references

Antityrosinase principles and constituents of the petals of Crocus sativus

Constituents of the stigmas of Crocus sativus and their tyrosinase inhibitory activity

Phenolic glucosides and a gamma-lactone glucoside from the sprouts of Crocus sativus

Constituents of the pollen of Crocus sativus L. and their tyrosinase inhibitory activity

Constituents of the Pollen of Crocus sativus L. and Their Tyrosinase Inhibitory Activity.

Cucumis sativus

2 references

Two new megastigmanes from the leaves of Cucumis sativus

Inhibitory effect of Cucumis sativus on melanin production in melanoma B16 cells by downregulation of tyrosinase expression

Dioscorea oppositifolia

2 references

A new phenanthrene glycoside and other constituents from Dioscorea opposita.

A New Phenanthrene Glycoside and Other Constituents from Dioscorea opposita.

Gastrodia elata

1 reference

Neuroprotective Principles from Gastrodia elata

Junceella juncea

1 reference

Study on the chemical constituents of the South China Sea gorgonian Junceella juncea

Oxytropis myriophylla

2 references

New flavonoids from Oxytropis myriophylla

New Flavonoids from Oxytropis myriophylla.

Strychnos lucida

1 reference

A quinic acid ester from Strychnos lucida

Subergorgia suberosa

2 references

Purine and pyrimidine derivatives from the South China Sea gorgonian Subergorgia suberosa

Purine alkaloids from the South China Sea gorgonian Subergorgia suberosa

maize

1 reference

Chemical constituents of the style of Zea mays L. with glycation inhibitory activity

Nigrospora sphaerica

1 reference

Nigrosphaerin A a new isochromene derivative from the endophytic fungus Nigrospora sphaerica

Oligomeris linifolia

1 reference

Phytochemical investigation of Oligomeris linifolia (Vahl) Macbr. (Resedaceae)

Eleutherococcus giraldii

1 reference

Chemical constituents from Acanthopanax brachypus

Alangium platanifolium

1 reference

Two phenolic glucosides and an iridoid glucoside from Alangium platanifolium var. Trilobum

Allium chinense

2 references

Effects of Chinese drugs "xiebai" and "dasuan" on human platelet aggregation (Allium bakeri, A. sativum)

Furostanol glycosides from bulbs of Allium chinense

Allium cepa

2 references

Antiplatelet constituents of garlic and onion

Isolation and identification of the platelet aggregation inhibitor present in the onion,Allium cepa

garlic

2 references

Antiplatelet constituents of garlic and onion

Effects of Chinese drugs "xiebai" and "dasuan" on human platelet aggregation (Allium bakeri, A. sativum)

Angelica acutiloba

1 reference

Evaluation of Angelicae Radix (Touki) by the Inhibitory Effect on Platelet Aggregation

Angelica archangelica

1 reference

Dihydrofurocoumarin glucosides from Angelica archangelica and Angelica silvestris

Angelica dahurica

1 reference

Coumarin glycosides from the roots ofAngelica dahurica

Ashitaba

1 reference

Three New Chalcones from the Aerial Parts ofAngelica keiskei

Argemone mexicana

1 reference

Cytotoxic benzophenanthridine and benzylisoquinoline alkaloids from Argemone mexicana.

Asterias forbesi

1 reference

Forbesin: A Novel Sulfated Glycolipid from the Starfish Asterias forbesi

Carthamus tinctorius

1 reference

[Identification and determination of platelet aggregation inhibitor from safflower (Carthamus tinctorius Linné)]

Senna tora

1 reference

A rubrofusarin gentiobioside isomer from roastedCassia tora

Cliona celata

1 reference

Isonitenin and Acetylhomoagmatine new Metabolites from the SpongesSpongia OfficinalisandCliona celatacollected at the Galician Coast (NW Spain)

Coix lacryma-jobi

1 reference

Phenolic compounds from Coix lachryma-jobi var. Ma-yuen

Ophiocordyceps sinensis

4 references

The fruiting body and its caterpillar host of Cordyceps sinensis show close resemblance in main constituents and anti-oxidation activity

Analysis of the Water Soluble Constituents ofCordyceps SinensisWith Heuristic Evolving Latent Projections

Medicinal Value of Cordyceps sinensis

Anti-inflammatory principles from Cordyceps sinensis

Coriandrum sativum

1 reference

Water-soluble constituents of coriander

Cucumis melo

1 reference

Identification of Platelet Inhibitor Present in the Melon (Cucurbitacea Cucumis Melo)

Melicope semecarpifolia

1 reference

Novel Acetophenones from Fruits of Evodia merrillii

Foeniculum vulgare

1 reference

Water-Soluble Constituents of Fennel. IX. Glucides and Nucleosides.

Fritillaria yuminensis

1 reference

Chemical constituents from Fritillaria anhuiensis

Ganoderma japonicum

1 reference

Identification and quantification of base and nucleoside markers in extracts of Ganoderma lucidum, Ganoderma japonicum and Ganoderma capsules by micellar electrokinetic chromatography.

Ganoderma lucidum

3 references

Central actions of adenosine, a nucleotide ofGanoderma lucidum

Identification and quantification of base and nucleoside markers in extracts of Ganoderma lucidum, Ganoderma japonicum and Ganoderma capsules by micellar electrokinetic chromatography.

Isolation of an inhibitor of platelet aggregation from a fungus, Ganoderma lucidum

Glehnia littoralis

2 references

Water-soluble constituents of Glehnia littoralis fruit

Constituents of the underground parts of Glehnia littoralis

Helichrysum arenarium

2 references

Medicinal flowers. XXVII. New flavanone and chalcone glycosides, arenariumosides I, II, III, and IV, and tumor necrosis factor-alpha inhibitors from everlasting, flowers of Helichrysum arenarium

Medicinal flowers. XXX. Eight new glycosides, everlastosides F-M, from the flowers of Helichrysum arenarium

Hemerocallis fulva

2 references

Lipid peroxidation inhibitory compounds from daylily (Hemerocallis fulva) leaves

Erratum to “Lipid peroxidation inhibitory compounds from daylily (Hemerocallis fulva) leaves” [Life Sciences 75 (2004) 753–763]

Ilex cornuta

1 reference

Triterpenoid glycosides from leaves of Ilex cornuta

Isatis tinctoria

3 references

Chemical consitituents from root of Isatis indigotica

A Novel Anthranilic Acid Derivative from Isatis tinctoria

Novel indole C-glycosides from Isatis indigotica and their potential cytotoxic activity

Juglans regia

1 reference

Antioxidative polyphenols from walnuts (Juglans regia L.).

Lactarius subplinthogalus

1 reference

Alkaloids from the fungus Lactarius subplinthogalus

Conioselinum anthriscoides

1 reference

Two phthalides from Ligusticum chuanxiong

Ligusticum chuanxiong

1 reference

Two phthalides from Ligusticum chuanxiong

Lilium mackliniae

1 reference

Studies on the Chemical Constituents of the Bulbs of Lilium mackliniae.

Lilium tenuifolium

1 reference

Lipid and steroidal constituents of Lilium auratum var. Platyphyllum AND L. tenuifolium

Marchantia polymorpha

1 reference

Phenanthrenes and other phenolics from in vitro cultures of Marchantia polymorpha

Medicago sativa

1 reference

Alfalfa (Medicago sativa L.) flavonoids. 1. Apigenin and luteolin glycosides from aerial parts.

Neptunea antiqua

1 reference

The toxin tetramine from the "edible" whelk Neptunea antiqua

Paeonia obovata

1 reference

New monoterpene glycoside esters and phenolic constituents of Paeoniae radix, and increase of water solubility of proanthocyanidins in the presence of paeoniflorin

Panax ginseng

2 references

Isolation of isomaltol-α-d-glucopyranoside1 and ketopropyl-α-d-glucopyranoside2 from Korean red ginseng

Application of high-speed liquid chromatography and dual wave-length thin-layer chromatograph-densitometry to analysis of crude drugs: Nucleosides and free bases of nucleic acids in Ginseng roots (author's transl)

Phaseolus vulgaris

1 reference

Cytokinin Biosynthesis in Phaseolus vulgaris Leaf Explants

Phoebe formosana

1 reference

Polar Chemical Constituents fromPhoebe formosana

Polygonatum sibiricum

1 reference

Isolation of Adenosine from the Rhizomes of Polygonatum sibidcum

Phlebodium decumanum

1 reference

Effects of Calaguala and an active principle, adenosine, on platelet activating factor

Portulaca oleracea

3 references

Alkaloids from Portulaca oleracea L.

Alkaloids from Portulaca oleracea L.

Alkaloids from Portulaca oleracea L.

Pseudomyrmex triplarinus

1 reference

Inhibition of human platelet aggregation and secretion by ant venom and a compound isolated from venom

Saposhnikovia divaricata

1 reference

Chemical constituents of roots of Saposhnikovia divaricata

Smilax bracteata

1 reference

New phenolic constituents from Smilax bracteata

Solanum incanum

2 references

Non-alkaloidal constituents from Solanum torvum leaves

Nonsteroidal Constituents fromSolanum IncanumL.

Scaphium affine

1 reference

Alkaloids from the Seeds of Sterculia lychnophora (Pangdahai).

Tethya aurantia

1 reference

Isolation of allantoin and adenosine from the marine sponge Tethya aurantia

Tethya aurantium

1 reference

Isolation of allantoin and adenosine from the marine sponge Tethya aurantia

Tetradium glabrifolium

1 reference

Constituents of Leaves of Tetradium Glabrifolium

Torilis japonica

1 reference

New Hemiterpenoid Pentol and Monoterpenoid Glycoside of Torillis japonica Fruit, and Consideration of the Origin of Apiose.

1 reference

1 reference

A comprehensive genome-scale reconstruction of Escherichia coli metabolism--2011.

Streptomyces piomogenus

2 references

Venturicidin C, a new 20-membered macrolide produced by Streptomyces sp. TS-2-2.

Penicisteroid C: New polyoxygenated steroid produced by co-culturing of Streptomyces piomogenus with Aspergillus niger

Albugo candida

1 reference

Phytoalexins and polar metabolites from the oilseeds canola and rapeseed: differential metabolic responses to the biotroph Albugo candida and to abiotic stress

Alternaria alternata

1 reference

Metabolites produced by an endophyte Alternaria alternata isolated from Maytenus hookeri

Aplysia kurodai

1 reference

Studies on the constituents of marine opisthobranchia, II. Structures of the new diacylglyceryl ether and cholesteryl ester mixture, and of three nucleosides from fertilized eggs of the sea hareAplysia kurodai

Azadirachta indica

1 reference

Secondary metabolites of endophytic fungus Xylaria sp. YC-10 of Azadirachta indica

Brachystemma calycinum

1 reference

Brachystemols A-C, three new furan derivatives from Brachystemma calycinum.

Brassica rapa

1 reference

Sinalexin, a phytoalexin from white mustard elicited by destruxin B and Alternaria brassicae

Broussonetia papyrifera

1 reference

N-containing compounds from Broussonetia papyrifera seeds and their cAMP regulatory activity in N1E-115 cells

Clitoria ternatea

1 reference

Chemische Untersuchung der Samen vonClitoria ternatea L.

Eurycoma longifolia

1 reference

Cytotoxic and antimalarial constituents from the roots of Eurycoma longifolia

Glinus oppositifolius

1 reference

L-(-)-(N-trans-Cinnamoyl)-arginine, an Acylamino Acid from Glinus oppositifolius (L.) Aug. DC

Gnaphalium polycaulon

1 reference

3-Hydroxydihydrobenzofuran glucosides from Gnaphalium polycaulon.

Hydrangea macrophylla

1 reference

New Cyanoglycosides, Hydracyanosides D, E, and F, from the Leaves of Hydrangea macrophylla

Kaempferia parviflora

1 reference

Structures of two new phenolic glycosides, kaempferiaosides A and B, and hepatoprotective constituents from the rhizomes of Kaempferia parviflora

Gymnosporia oxyphylla

1 reference

Metabolites produced by an endophyte Alternaria alternata isolated from Maytenus hookeri

Q15561302

1 reference

New constituents from Mikania laevigata Shultz Bip. ex Baker

moringa

1 reference

Unusual glycosides of pyrrole alkaloid and 4'-hydroxyphenylethanamide from leaves of Moringa oleifera

Morus alba

1 reference

Inhibitory effects of constituents from Morus alba var. multicaulis on differentiation of 3T3-L1 cells and nitric oxide production in RAW264.7 cells.

Morus alba var. multicaulis

1 reference

Inhibitory effects of constituents from Morus alba var. multicaulis on differentiation of 3T3-L1 cells and nitric oxide production in RAW264.7 cells.

Notechis scutatus

1 reference

Additional Purine Compounds in the Venom of the Tiger Snake (Notechis Scutatus)

Oryza aristata

1 reference

Anti-inflammatory and antioxidant components from Hygroryza aristata

Oxytropis racemosa

1 reference

3-Hydroxymethylglutaryl flavonol glycosides from a Mongolian and Tibetan medicine, Oxytropis racemosa

Common rose

1 reference

Aristolochic Acids as a Defensive Substance for the Aristolochiaceous Plant-Feeding Swallowtail Butterfly,Pachliopta aristolochiae interpositus

Panax japonicus

1 reference

Panajaponin, a new glycosphingolipid from Panax japonicus

Populus alba

1 reference

The complex of O-glucosylzeatin derivatives formed in Populus species

Prunus amygdalus

1 reference

Sphingolipid and other constituents from almond nuts (Prunus amygdalus Batsch).

Prunus dulcis

1 reference

Sphingolipid and other constituents from almond nuts (Prunus amygdalus Batsch).

Breynia androgyna

1 reference

Active Chemical Constituents fromSauropus androgynus

Sauropus androgynus

1 reference

Active Chemical Constituents fromSauropus androgynus

Tuber indicum

1 reference

Chemical constituents from the ascomycetous fungus Tuber indicum

Ulva pertusa

1 reference

Cardiac inhibitory action of constituents of the marine green alga Ulva pertusa

Paralepista flaccida

1 reference

Clitocine, a new insecticidal nucleoside from the mushroom clitocybe inversa

American ginseng

1 reference

Isolation and hypoglycemic activity of quinquefolans A, B, and C, glycans of Panax quinquefolium roots

Ulva australis

1 reference

Cardiac inhibitory action of constituents of the marine green alga Ulva pertusa

Gymnosporia acuminata

1 reference

Metabolites produced by an endophyte Alternaria alternata isolated from Maytenus hookeri

Bryobium erioides

1 reference

Structures of two new phenolic glycosides, kaempferiaosides A and B, and hepatoprotective constituents from the rhizomes of Kaempferia parviflora

Adiantum philippense

1 reference

A new triterpenoid from the fern Adiantum lunulatum and evaluation of antibacterial activity

Ligusticum striatum

1 reference

Two phthalides from Ligusticum chuanxiong

Euphoria longana

1 reference

Adenosine, the anxiolytic-like principle of the Arillus of Euphoria longana

Trachyspermum ammi

1 reference

Water-soluble constituents of ajowan

Oryza sativa

1 reference

Anti-inflammatory and antioxidant components from Hygroryza aristata

Cordyceps

1 reference

Natural Products as Antiviral Agents

Bryobium eriaeoides

1 reference

Structures of two new phenolic glycosides, kaempferiaosides A and B, and hepatoprotective constituents from the rhizomes of Kaempferia parviflora

Caenorhabditis elegans

1 reference

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

Streptomyces mutabilis

1 reference

N-Acetylborrelidin B: a new bioactive metabolite from Streptomyces mutabilis sp. MII.

Nigrospora oryzae

1 reference

Nigrosphaerin A a new isochromene derivative from the endophytic fungus Nigrospora sphaerica

Lilium pumilum

1 reference

Lipid and steroidal constituents of Lilium auratum var. Platyphyllum AND L. tenuifolium

Prunus avium

1 reference

Sphingolipid and other constituents from almond nuts (Prunus amygdalus Batsch).

Apiaceae

1 reference

[Studies on chemical protectors against radiation. XXX. Radioprotective substances of cnidii rhizoma]

Arabidopsis thaliana

1 reference

Metabolomics-oriented isolation and structure elucidation of 37 compounds including two anthocyanins from Arabidopsis thaliana

Chlamydomonas reinhardtii

1 reference

The response of Chlamydomonas reinhardtii to nitrogen deprivation: a systems biology analysis

Levisticum officinale

1 reference

[Studies on chemical protectors against radiation. XXX. Radioprotective substances of cnidii rhizoma]

Ligusticum officinale

1 reference

[Studies on chemical protectors against radiation. XXX. Radioprotective substances of cnidii rhizoma]

medical condition treated

paroxysmal tachycardia

1 reference

Wolff–Parkinson–White syndrome

13 December 2016

1 reference

physically interacts with

13 December 2016

Adenosine A1 receptor

2 references

17 August 2016

Open Targets Platform

14 August 2023

https://platform.opentargets.org/drug/CHEMBL477

Adenosine A2a receptor

1 reference

17 August 2016

Adenosine A2b receptor

2 references

17 August 2016

Open Targets Platform

14 August 2023

https://platform.opentargets.org/drug/CHEMBL477

Adenosine A3 receptor

2 references

17 August 2016

Open Targets Platform

14 August 2023

https://platform.opentargets.org/drug/CHEMBL477

Phosphatidylinositol 4-kinase type 2 alpha

1 reference

Phosphatidylinositol 4-kinase type 2 beta

17 August 2016

1 reference

Transient receptor potential cation channel subfamily M member 4

17 August 2016

1 reference

https://www.pfizer.com/products/product-list

17 August 2016

1 reference

described by source

Armenian Soviet Encyclopedia

volume

1

70

0 references

1 reference

1 reference

15 March 2018

1 reference

15 March 2018

1 reference

MeSH descriptor ID

D000241

purinergic P1 receptor agonist

15 March 2018

1 reference

https://reactome.org/PathwayBrowser/#/R-HSA-1430728&DTAB=MT

15 March 2018

1 reference

0 references

0 references

0 references

Adenosine

1 reference

imported from Wikimedia project

German Wikipedia

topic's main category

Category:Adenosine

0 references

catalog

CAS COVID-19 Anti-Viral Candidate Compounds

0 references

P7049 (Deleted Property)

595 Property P7049 not found, cannot determine the data type to use.

0 references

Identifiers

Bibliothèque nationale de France ID

121238390

Adénosine

1 reference

Nuovo soggettario

https://thes.bncf.firenze.sbn.it/termine.php?id=47130

16 June 2021

Adenosin

1 reference

Nuovo soggettario

https://thes.bncf.firenze.sbn.it/termine.php?id=47130

16 June 2021

1 reference

National Library of Israel

Library of Congress authority ID

sh85000846

Adenosine

1 reference

Nuovo soggettario

https://thes.bncf.firenze.sbn.it/termine.php?id=47130

16 June 2021

0 references

adenosin

0 references

InChI

InChI=1S/C10H13N5O4/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(18)6(17)4(1-16)19-10/h2-4,6-7,10,16-18H,1H2,(H2,11,12,13)/t4-,6-,7-,10-/m1/s1

1 reference

OIRDTQYFTABQOQ-KQYNXXCUSA-N

adenosine (English)

19 November 2016

2 references

adenosine (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

58-61-7

2 references

OIRDTQYFTABQOQ-KQYNXXCUSA-N

adenosine (English)

19 November 2016

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=58-61-7

1 reference

Adenosine (English)

19 November 2016

1 reference

adenosine (English)

19 November 2016

Reaxys registry number

93029

1 reference

adenosine (English)

19 October 2016

53385

0 references

ChEBI ID

16335

mapping relation type

2 references

ADENOSINE (English)

19 November 2016

ChEBI release 2019-10-02

1 reference

Cambridge Structural Database

ADENOSINE (English)

19 November 2016

1 reference

Cambridge Structural Database

1101224 (English)

4 January 2023

1 reference

10 January 2023

1 reference

Cambridge Structural Database

MSBNK-BGC_Munich-RP010901

10 January 2023

based on heuristic

InChIKey match

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

MSBNK-BGC_Munich-RP010902

0 references

MSBNK-BGC_Munich-RP010903

0 references

MSBNK-Fiocruz-FIO00683

0 references

MSBNK-Fiocruz-FIO00684

0 references

MSBNK-Fiocruz-FIO00685

0 references

MSBNK-Fiocruz-FIO00686

0 references

MSBNK-Fiocruz-FIO00687

0 references

MSBNK-Keio_Univ-KO008860

0 references

MSBNK-Keio_Univ-KO008861

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000141

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000142

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000143

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000144

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000145

0 references

0 references

0 references

0 references

0 references

MSBNK-Osaka_Univ-OUF00097

0 references

0 references

0 references

0 references

0 references

0 references

MSBNK-Washington_State_Univ-BML80690

0 references

MSBNK-Washington_State_Univ-BML80691

0 references

MSBNK-Washington_State_Univ-BML80692

0 references

MSBNK-Washington_State_Univ-BML80693

0 references

MSBNK-IPB_Halle-PB006009

0 references

MSBNK-IPB_Halle-PB006010

0 references

MSBNK-IPB_Halle-PB006011

0 references

MSBNK-Kazusa-KZ000013

0 references

MSBNK-Kazusa-KZ000106

0 references

MSBNK-Keio_Univ-KO000009

0 references

MSBNK-Keio_Univ-KO000010

0 references

MSBNK-Keio_Univ-KO000011

0 references

MSBNK-Keio_Univ-KO000012

0 references

MSBNK-Keio_Univ-KO000013

0 references

MSBNK-Keio_Univ-KO002038

0 references

MSBNK-Keio_Univ-KO002039

0 references

MSBNK-Keio_Univ-KO002040

0 references

MSBNK-Keio_Univ-KO002041

0 references

MSBNK-Keio_Univ-KO002042

0 references

SPLASH

splash10-000i-0900000000-38a0b51e84259a90e0bf

0 references

splash10-000i-0900000000-95ff80024f6f3ecb8b96

0 references

splash10-000i-0900000000-54121dd1ddff8baeedbd

0 references

splash10-000i-0900000000-bc944eede02f73a9f09c

0 references

splash10-000i-1900000000-bf97b22e23b479deb25b

0 references

splash10-001i-0910000000-65268017a112bc263b5e

0 references

splash10-001i-0900000000-375c0e137f7068cf49af

0 references

splash10-001i-0900000000-ad5db8e5cbaacc341347

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splash10-001i-0900000000-718be441310a581854a6

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splash10-053r-2900000000-2f0ca594f7cc031e54e7

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splash10-014i-0490000000-47f7a73ecc9fc3610eac

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splash10-000i-0900000000-e43eddf41f22caa830b7

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splash10-00kr-0960000000-c27288ef88b7c9fada7c

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splash10-0f7w-1890000000-5c70a5423faa5e8eceaf

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splash10-001i-0910000000-815ed65588c07415cd65

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splash10-000i-0900000000-f0313435db4847490fd6

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splash10-000i-1900000000-23bcec0b5be3fa4e10ed

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splash10-000i-2900000000-60219ac7d9220e297492

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splash10-000i-0900000000-cda34117888d584ca7b7

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splash10-000i-0900000000-0591143763a0bad31c23

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splash10-000i-0910000000-83e1685b54e8f76906fd

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splash10-000i-0920000000-985897f3309c69d2acfb

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splash10-000i-0930000000-9e6777212cb3a21a3a83

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splash10-000i-0940000000-a9e90a868ea4f0f6fdb3

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splash10-014i-0090000000-d6b9d4e675ce74fb69dc

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splash10-014i-0090000000-3d4fd8ea211eaed10531

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splash10-000i-0900000000-cb58ec56a5faa09c9a02

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splash10-000i-0900000000-9559aa07ec13a688fb16

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splash10-000i-0900000000-f7c1371d8e1058df3a32

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splash10-001s-0790000000-cc3bcd977e11efd4ea25

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splash10-00di-9460000000-3ae19bfaa5d2df72f9b1

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splash10-014i-0290000000-f1d71a97ce39145c8e31

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splash10-00kr-0950000000-9bbdbb14aed287ad5ac8

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splash10-001i-0910000000-35f90965f1f3c2b3236b

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splash10-000i-0900000000-f360cca994696d7ae735

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splash10-014i-0090000000-e45b10977afb4031566e

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splash10-004i-0049000000-7eae9746bf0400ecf3fd

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splash10-014i-0090000000-cbf52f09923610b14678

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splash10-001i-0980000000-010ad268f6f16387f258

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splash10-001i-0980000000-b6ccd0b3c3f1e4609b70

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splash10-001i-3900000000-184bc35fdd2d4f31811d

0 references

splash10-001i-4900000000-f7109d5962d68f9d3d86

0 references

splash10-014i-0090000000-2b10185f8de8aa3a8f47

0 references

splash10-014i-0090000000-6f44f039f9e279594114

0 references

splash10-000i-0900000000-651d15ab9b662a38b492

0 references

splash10-000i-0900000000-a402d2ca713675531013

0 references

splash10-02t9-0294000000-e776813b8673c26fe18d

0 references

splash10-014i-0092000000-a5996ce971533028297b

0 references

splash10-03fr-0039520000-8021ef4e301e389ac354

0 references

splash10-01t9-0039810000-793f4050aa5f99e309c2

0 references

splash10-000i-0900000000-2c0e6b8a728abdb47a39

0 references

splash10-014i-0090000000-073ffdbbe1c5e2e29ca5

0 references

splash10-000i-0910000000-d78a44484ff5b14b419f

0 references

splash10-000i-0900000000-7674c1e40b334d40ecbe

0 references

splash10-000i-0900000000-bfe27ee84cb1083dae1b

0 references

splash10-000i-0900000000-22db9d5dbb8f445190a5

0 references

splash10-000i-0900000000-b8f21fed9413cbd807ca

0 references

splash10-014i-0090000000-b3dc03a79d4d703a5b17

0 references

splash10-000i-0900000000-f07c24472aac1999a0d3

0 references

splash10-000i-0900000000-bacac411b20c5f77349a

0 references

splash10-000i-0900000000-6d9ae97da08108dcf977

0 references

splash10-000i-0900000000-7c4041777d54eb7175cb

0 references

splash10-0gc0-0590000000-05874cecded3009c1f4d

0 references

splash10-0fsv-1792000000-b37fd6826f28aaf9e825

0 references

splash10-000i-1900000000-dd7cbed8e76c6e783831

0 references

splash10-000i-2900000000-c6644520b5943b59403d

0 references

splash10-014r-0890000000-588861a9494ab4680698

0 references

HSDB ID

7774

1 reference

Hazardous Substances Data Bank

28 October 2019

Adenosine (English)

10 May 2021

1 reference

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

DSSTOX compound identifier

0 references

0 references

0 references

1 reference

adenosine (English)

ECHA Substance Infocard ID

19 November 2016

100.000.354

1 reference

http://echa.europa.eu/de/information-on-chemicals/registered-substances

1 reference

28 December 2019

ADENOSINE (English)

CAS no.: 58-61-7 (English)

1 reference

1 reference

Adenosine (English)

publication date

17 November 2015

1 reference

adenosine (English)

19 November 2016

Adenosine

0 references

MeSH tree code

D03.633.100.759.590.138

0 references

0 references

0 references

1 reference

adenosine (English)

19 November 2016

1 reference

Adenosine (English)

Human Metabolome Database ID

19 November 2016

0 references

1 reference

adenosine (English)

19 October 2016

1 reference

adenosine (English)

19 November 2016

1 reference

adenosine (English)

19 November 2016

0 references

1 reference

Immune Epitope Database and Analysis Resource

adenosine (English)

19 October 2016

0 references

1 reference

1 January 2022

0 references

1 reference

National Central Library of Florence

0 references

0 references

1 reference

28 October 2013

Gran Enciclopèdia Catalana ID (former scheme)

0219762

0 references

LEM ID

LEM201000143

0 references

Microsoft Academic ID

2776991684

0 references

NALT ID

4142

0 references

OmegaWiki Defined Meaning

1229006

0 references

Online PWN Encyclopedia ID

0 references

1 reference

26 January 2022

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

1 reference

4LCA (English)

19 October 2016

1 reference

4LC4 (English)

19 October 2016

1 reference

3KW2 (English)

19 October 2016

1 reference

3UAY (English)

19 October 2016

1 reference

3UAW (English)

19 October 2016

1 reference

4IMA (English)

19 October 2016

1 reference

1FMO (English)

19 October 2016

1 reference

2JC9 (English)

19 October 2016

1 reference

1DGM (English)

19 October 2016

1 reference

4JKU (English)

19 October 2016

1 reference

4JKS (English)

19 October 2016

1 reference

3G1U (English)

19 October 2016

1 reference

1Q97 (English)

19 October 2016

1 reference

1PG2 (English)

19 October 2016

1 reference

1YI4 (English)

19 October 2016

1 reference

4X3M (English)

19 October 2016

1 reference

2B82 (English)

19 October 2016

1 reference

2GL0 (English)

19 October 2016

1 reference

4DC3 (English)

19 October 2016

1 reference

4D9H (English)

19 October 2016

1 reference

1XWF (English)

19 October 2016

1 reference

4O0W (English)

19 October 2016

1 reference

4O0U (English)

19 October 2016

1 reference

4O0S (English)

19 October 2016

1 reference

5A1I (English)

19 October 2016

1 reference

4LBX (English)

19 October 2016

1 reference

4LBG (English)

19 October 2016

1 reference

3UQ6 (English)

19 October 2016

1 reference

3GRV (English)

19 October 2016

1 reference

2KQD (English)

19 October 2016

1 reference

2KQE (English)

19 October 2016

1 reference

1MUO (English)

19 October 2016

1 reference

2X0P (English)

19 October 2016

1 reference

2PKM (English)

19 October 2016

1 reference

4K87 (English)

19 October 2016

1 reference

4K8P (English)

19 October 2016

1 reference

4K8T (English)

19 October 2016

1 reference

4K8C (English)

19 October 2016

1 reference

4K8K (English)

19 October 2016

1 reference

3REQ (English)

19 October 2016

1 reference

4E3A (English)

19 October 2016

1 reference

3AY0 (English)

19 October 2016

1 reference

3F8W (English)

19 October 2016

1 reference

1PK7 (English)

19 October 2016

1 reference

1Z37 (English)

19 October 2016

1 reference

5HJI (English)

19 October 2016

1 reference

3O1X (English)

19 October 2016

1 reference

3O1C (English)

19 October 2016

1 reference

4CKJ (English)

19 October 2016

1 reference

4CKI (English)

19 October 2016

1 reference

4PFJ (English)

19 October 2016

1 reference

1HO5 (English)

19 October 2016

1 reference

1JDV (English)

19 October 2016

1 reference

1MRG (English)

19 October 2016

1 reference

1N3Z (English)

19 October 2016

1 reference

4K9C (English)

19 October 2016

1 reference

4K9I (English)

19 October 2016

1 reference

4K93 (English)

19 October 2016

1 reference

4OGR (English)

19 October 2016

1 reference

2X1L (English)

19 October 2016

1 reference

4UCI (English)

19 October 2016

1 reference

4KBE (English)

19 October 2016

1 reference

4LVC (English)

19 October 2016

1 reference

3AXZ (English)

19 October 2016

1 reference

4XJ7 (English)

19 October 2016

1 reference

2ZGW (English)

19 October 2016

1 reference

1WU8 (English)

19 October 2016

1 reference

4IP7 (English)

19 October 2016

1 reference

2EVA (English)

19 October 2016

1 reference

3O0Q (English)

19 October 2016

1 reference

3H9U (English)

19 October 2016

1 reference

1BX4 (English)

19 October 2016

1 reference

2C49 (English)

19 October 2016

1 reference

4PEV (English)

19 October 2016

1 reference

2A8T (English)

19 October 2016

1 reference

1MRJ (English)

19 October 2016

1 reference

3OI8 (English)

19 October 2016

1 reference

4KTV (English)

19 October 2016

1 reference

3VAQ (English)

19 October 2016

1 reference

3VAS (English)

19 October 2016

1 reference

3N58 (English)

19 October 2016

1 reference

1ODI (English)

19 October 2016

1 reference

3FUU (English)

19 October 2016

1 reference

4XDR (English)

19 October 2016

1 reference

2OA1 (English)

19 October 2016

1 reference

2W03 (English)

19 October 2016

1 reference

4O8J (English)

19 October 2016

1 reference

1RMT (English)

19 October 2016

1 reference

2FQY (English)

19 October 2016

1 reference

4DTA (English)

19 October 2016

1 reference

1V8B (English)

19 October 2016

1 reference

1LII (English)

19 October 2016

1 reference

1LIK (English)

19 October 2016

1 reference

4PD9 (English)

19 October 2016

1 reference

3CE6 (English)

19 October 2016

1 reference

1D4F (English)

19 October 2016

1 reference

5AQF (English)

19 October 2016

1 reference

5AXA (English)

19 October 2016

1 reference

2EJG (English)

19 October 2016

1 reference

2EJF (English)

19 October 2016

1 reference

3OND (English)

19 October 2016

1 reference

2B8J (English)

19 October 2016

1 reference

2YDO (English)

19 October 2016

1 reference

3WDM (English)

19 October 2016

1 reference

5AQY (English)

19 October 2016

1 reference

1VHW (English)

19 October 2016

1 reference

5HM8 (English)

19 October 2016

1 reference

2DOJ (English)

19 October 2016

1 reference

4ZME (English)

19 October 2016

1 reference

3QWU (English)

19 October 2016

1 reference

3UBO (English)

19 October 2016

1 reference

4PGF (English)

19 October 2016

1 reference

2Q6K (English)

19 October 2016

1 reference

4N09 (English)

19 October 2016

1 reference

3QGZ (English)

19 October 2016

1 reference

2ZBV (English)

19 October 2016

1 reference

2ZBU (English)

19 October 2016

1 reference

1JG2 (English)

19 October 2016

1 reference

1JG3 (English)

19 October 2016

1 reference

4H2F (English)

19 October 2016

1 reference

4H2G (English)

19 October 2016

1 reference

2AC7 (English)

19 October 2016

1 reference

2PGF (English)

19 October 2016

1 reference

4DT8 (English)

19 October 2016

1 reference

3ZTV (English)

19 October 2016

1 reference

4KAH (English)

19 October 2016

1 reference

4KAL (English)

19 October 2016

1 reference

4KAN (English)

19 October 2016

1 reference

4KAD (English)

19 October 2016

1 reference

2Q83 (English)

19 October 2016

1 reference

1UAY (English)

19 October 2016

1 reference

agricultural-and-biological-sciences/adenosine

3U40 (English)

19 October 2016

1 reference

ScienceDirect topic ID

0 references

chemical-engineering/adenosine

0 references

chemistry/adenosine

0 references

earth-and-planetary-sciences/adenosine

0 references

engineering/adenosine

0 references

medicine-and-dentistry/adenosine

0 references

nursing-and-health-professions/adenosine

0 references

pharmacology-toxicology-and-pharmaceutical-science/adenosine

0 references

psychology/adenosine

0 references

social-sciences/adenosine

0 references

physics-and-astronomy/adenosines

0 references

Semantic Scholar topic ID

0 references

adenosina

0 references

Treccani's Dizionario delle Scienze Fisiche ID

adenosina

Treccani's Dizionario di Medicina ID

adenosina

publication date

1996

0 references

adenosina

adenosina

publication date

2010

0 references

UMLS CUI

C0001443

1 reference

adenosine (English)

19 November 2016

0 references

WordNet 3.1 Synset ID

14731262-n

1 reference

adenosiini

adenosin

adenosine

1 reference

YSO-Wikidata mapping project