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ChEBI
> Main
CHEBI:17596 - inosine
Main
ChEBI Ontology
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ChEBI Name
inosine
ChEBI ID
CHEBI:17596
Definition
A purine nucleoside in which hypoxanthine is attached to ribofuranose via a β-
N
9
-glycosidic bond.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:44407, CHEBI:5927, CHEBI:14456, CHEBI:24841
Supplier Information
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Molfile
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Wikipedia
License
Read full article at Wikipedia
Formula
C10H12N4O5
Net Charge
0
Average Mass
268.22610
Monoisotopic Mass
268.08077
InChI
InChI=1S/C10H12N4O5/c15-
1-
4-
6(16)
7(17)
10(19-
4)
14-
3-
13-
5-
8(14)
11-
2-
12-
9(5)
18/h2-
4,6-
7,10,15-
17H,1H2,(H,11,12,18)
/t4-
,6-
,7-
,10-
/m1/s1
InChIKey
UGQMRVRMYYASKQ-KQYNXXCUSA-N
SMILES
OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(O)ncnc12
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
Source: BioModels - MODEL1507180067 See:
PubMed
Saccharomyces cerevisiae
(NCBI:txid4932)
Source: yeast.sf.net See:
PubMed
Escherichia coli
(NCBI:txid562)
See:
PubMed
Homo sapiens
(NCBI:txid9606)
See:
DOI
Roles Classification
Biological Role
(s):
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in
Escherichia coli
.
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (
Saccharomyces cerevisiae
).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
inosine (
CHEBI:17596
)
has functional parent
hypoxanthine (
CHEBI:17368
)
inosine (
CHEBI:17596
)
has functional parent
ribofuranose (
CHEBI:46998
)
inosine (
CHEBI:17596
)
has role
Escherichia coli
metabolite (
CHEBI:76971
)
inosine (
CHEBI:17596
)
has role
Saccharomyces cerevisiae
metabolite (
CHEBI:75772
)
inosine (
CHEBI:17596
)
has role
human metabolite (
CHEBI:77746
)
inosine (
CHEBI:17596
)
has role
mouse metabolite (
CHEBI:75771
)
inosine (
CHEBI:17596
)
is a
inosines (
CHEBI:24844
)
inosine (
CHEBI:17596
)
is a
purines
D
-ribonucleoside (
CHEBI:142355
)
Incoming
1-methylinosine (
CHEBI:19065
)
has functional parent
inosine (
CHEBI:17596
)
2ʼ-deoxyinosine (
CHEBI:28997
)
has functional parent
inosine (
CHEBI:17596
)
2'-
O
-methylinosine (
CHEBI:68467
)
has functional parent
inosine (
CHEBI:17596
)
3',5'-cyclic IMP (
CHEBI:27541
)
has functional parent
inosine (
CHEBI:17596
)
5'-
S
-methyl-5'-thioinosine (
CHEBI:48595
)
has functional parent
inosine (
CHEBI:17596
)
5'-deoxyinosine (
CHEBI:82775
)
has functional parent
inosine (
CHEBI:17596
)
6-
O
-methylinosine (
CHEBI:70972
)
has functional parent
inosine (
CHEBI:17596
)
6-deoxyinosine 5'-phosphate (
CHEBI:45262
)
has functional parent
inosine (
CHEBI:17596
)
7-methylinosine (
CHEBI:70971
)
has functional parent
inosine (
CHEBI:17596
)
Phosphoric acid mono-[(2R,3S,4R,5R)-5-(6-amino-purin-9-yl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethyl] ester (
CHEBI:193717
)
has functional parent
inosine (
CHEBI:17596
)
IUPAC Names
(2
R
,3
S
,4
R
,5
R
)-
2-
(hydroxymethyl)-
5-
(6-
hydroxy-
9
H
-
purin-
9-
yl)tetrahydrofuran-
3,4-
diol
9-(β-
D
-ribofuranosyl)-9
H
-purin-6-ol
inosine
INNs
Sources
inosina
ChemIDplus
inosine
ChemIDplus
inosinum
ChemIDplus
Synonyms
Sources
9-β-
D
-ribofuranosyl-9
H
-purin-6-ol
IUPAC
9-β-
D
-ribofuranosylhypoxanthine
NIST Chemistry WebBook
hypoxanthine
D
-riboside
ChemIDplus
hypoxanthosine
ChemIDplus
i
ChEBI
Inosin
ChEBI
Inosine
KEGG COMPOUND
INOSINE
PDBeChem
inosine
UniProt
Manual Xrefs
Databases
3301
DrugCentral
C00019692
KNApSAcK
C00294
KEGG COMPOUND
D00054
KEGG DRUG
ECMDB00195
ECMDB
HMDB0000195
HMDB
Inosine
Wikipedia
INOSINE
MetaCyc
NOS
PDBeChem
YMDB00510
YMDB
View more database links
Registry Numbers
Types
Sources
489332
Gmelin Registry Number
Gmelin
58-63-9
CAS Registry Number
ChemIDplus
58-63-9
CAS Registry Number
NIST Chemistry WebBook
624889
Reaxys Registry Number
Reaxys
Citation
Type
Source
22770225
PubMed citation
Europe PMC
Last Modified
22 February 2017