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Substance
ID:1824204
Structure
Similarity
Functional Group
Text
ID:690
ribavirin
Chemical Entities of Biological Interest
ID: CHEBI:63580
Names and Identifiers
IUPAC name
1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1H-1,2,4-triazole-3-carboxamide
IUPAC Traditional name
ribavirin
Synonyms
ribavirin
1-beta-D-Ribofuranosyl-1,2,4-triazole-3-carboxamide
1-beta-D-Ribofuranosyl-1H-1,2,4-triazole-3-carboxamide
RBV
International Nonproprietary Name (INN)
ribavirin
ribavirina
ribavirine
ribavirinum
Registration numbers
CAS Number
36791-04-5
PubChem CID
37542
DrugBank ID
DB00811
LINCS Database
LSM-5701
PubMed Citation Links
29438107
22212579
21827730
22052220
22239511
22212566
22212569
22212576
22212568
22156853
22212572
22158703
22220723
22239498
22052088
Reaxys Registry
892462
ACToR Database
36791-04-5
BKMS React Database
239340
1304
101995
BRENDA Database
2.4.2.1
2.1.1.57
3.4.21.98
2.1.1.56
3.3.1.1
7.6.2.1
1.1.1.205
2.4.2.4
2.7.1.113
2.7.1.76
2.7.7.48
3.1.3.5
2.7.1.20
2.7.1.B20
3.5.4.4
2.4.2.2
1.1.3.39
2.7.1.48
2.7.7.84
BRENDA Ligand Database
239340
101995
1304
CHEMBL
CHEMBL1643
CompTox Database
DTXSID8023557
MetaboLights Database
MTBLS3950
MTBLS3750
Protein Data Bank
3sfu
4pb1
5axd
SABIO-RK Database
8119
SureChEMBL Database
SCHEMBL3727
UniProt Database
P12268
P04936
P03300
Q82081
P07210
P03301
P06210
P23069
P06209
P03302
Q82122
P23008
P12916
O41174
Q86887
P08292
Q03053
Q9QL88
P36290
P21404
P08291
Q9YLG5
P03313
Q66282
P16604
P13900
Q66474
Q66577
Q66849
P29813
Q66575
Q9WN78
O91734
Q9YLJ1
P12915
Q9QF31
P22055
Q65900
P03303
P32537
Q66478
Q66479
P20839
Q9UA35
Q9HAS3
Q9ERH8
Q8VIH3
Beilstein Number
892462
Wikipedia Title
Ribavirin
GeneOntology Database
GO:1901559
Drug Central Database
2,373
BindingDB Database
50154375
KEGG DRUG Database
D00423
ArrayExpress (Gene Expression Altlas)
E-GEOD-23031
CHEBI ID
CHEBI:63580
CHEBI:8840
PubChem SID
135610122
Properties
No Data Available
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Molecule Details
A 1-ribosyltriazole that is the 1-ribofuranosyl derivative of 1,2,4-triazole-3-carboxamide. A synthetic guanosine analogue, it is an inhibitor of HCV polymerase and possesses a broad spectrum of activity against DNA and RNA viruses.
Molecular Spectra
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References
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