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ChEBI
> Main
CHEBI:147675 - 5-iodo-2'-deoxyuridine
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ChEBI Ontology
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ChEBI Name
5-iodo-2'-deoxyuridine
ChEBI ID
CHEBI:147675
Definition
A pyrimidine 2'-deoxyribonucleoside compound having 5-iodouracil as the nucleobase; used as an antiviral agent.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:43233, CHEBI:5863
Supplier Information
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Formula
C9H11IN2O5
Net Charge
0
Average Mass
354.09850
Monoisotopic Mass
353.97127
InChI
InChI=1S/C9H11IN2O5/c10-
4-
2-
12(9(16)
11-
8(4)
15)
7-
1-
5(14)
6(3-
13)
17-
7/h2,5-
7,13-
14H,1,3H2,(H,11,15,16)
/t5-
,6+,7+/m0/s1
InChIKey
XQFRJNBWHJMXHO-RRKCRQDMSA-N
SMILES
OC[C@H]1O[C@H](C[C@@H]1O)n1cc(I)c(=O)[nH]c1=O
Roles Classification
Biological Role
(s):
antiviral drug
A substance used in the prophylaxis or therapy of virus diseases.
DNA synthesis inhibitor
Any substance that inhibits the synthesis of DNA.
Application
(s):
antiviral drug
A substance used in the prophylaxis or therapy of virus diseases.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
5-iodo-2'-deoxyuridine (
CHEBI:147675
)
has role
antiviral drug (
CHEBI:36044
)
5-iodo-2'-deoxyuridine (
CHEBI:147675
)
has role
DNA synthesis inhibitor (
CHEBI:59517
)
5-iodo-2'-deoxyuridine (
CHEBI:147675
)
is a
organoiodine compound (
CHEBI:37142
)
5-iodo-2'-deoxyuridine (
CHEBI:147675
)
is a
pyrimidine 2'-deoxyribonucleoside (
CHEBI:19255
)
IUPAC Name
2'-deoxy-5-iodouridine
INNs
Sources
idoxuridina
ChemIDplus
idoxuridine
WHO MedNet
idoxuridine
ChemIDplus
Idoxuridinum
ChemIDplus
Synonyms
Sources
(+)-5-Iodo-2'-deoxyuridine
NIST Chemistry WebBook
1-(2-Deoxy-beta-D-ribofuranosyl)-5-iodouracil
ChemIDplus
1-beta-D-2'-Deoxyribofuranosyl-5-iodouracil
ChemIDplus
1beta-D-2'-Deoxyribofuranosyl-5-iodouracil
ChemIDplus
2'-Deoxy-5-iodouridine
ChemIDplus
5-Iododeoxyuridine
DrugBank
5-Iodouracil deoxyriboside
ChemIDplus
Idoxuridin
ChemIDplus
IdU
ChEBI
Iododeoxyridine
ChemIDplus
Iodoxuridine
ChemIDplus
Joddeoxiuridin
ChemIDplus
Manual Xrefs
Databases
1417
DrugCentral
DB03778
DrugBank
LSM-5836
LINCS
View more database links
Registry Numbers
Types
Sources
30397
Reaxys Registry Number
Reaxys
54-42-2
CAS Registry Number
ChemIDplus
54-42-2
CAS Registry Number
NIST Chemistry WebBook
Citations
Types
Sources
17341060
PubMed citation
ChEMBL
17438061
PubMed citation
ChEMBL
18555978
PubMed citation
Europe PMC
3950402
PubMed citation
Europe PMC
Last Modified
06 March 2017