CHEBI:147675 - 5-iodo-2'-deoxyuridine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
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
Download Molfile XML SDF
more structures >>
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 Waiting for 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