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Details

Stereochemistry ABSOLUTE
Molecular Formula C8H13N4O8P
Molecular Weight 324.1846
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RIBAVIRIN MONOPHOSPHATE

SMILES

NC(=O)C1=NN(C=N1)[C@@H]2O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]2O

InChI

InChIKey=SDWIOXKHTFOULX-AFCXAGJDSA-N
InChI=1S/C8H13N4O8P/c9-6(15)7-10-2-12(11-7)8-5(14)4(13)3(20-8)1-19-21(16,17)18/h2-5,8,13-14H,1H2,(H2,9,15)(H2,16,17,18)/t3-,4-,5-,8-/m1/s1

HIDE SMILES / InChI

Molecular Formula C8H13N4O8P
Molecular Weight 324.1846
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis and antiviral acticity of some phosphates of the broad-spectrum antiviral nucleoside, 1-beta-D-ribofuranosyl-1,2,4-triazole-3-carboxamide (ribavirin).
1978 Aug
Synthesis and antiviral and enzymatic studies of certain 3-deazaguanines and their imidazolecarboxamide precursors.
1978 Dec
Inhibition of rotaviruses by selected antiviral substances: mechanisms of viral inhibition and in vivo activity.
1982 Jan
Inhibition of herpes simplex virus DNA polymerase by purine ribonucleoside monophosphates.
1986 Feb 5
A newly developed immunofluorescent assay for determining the Pichinde virus-inhibitory effects of selected nucleoside analogues.
1988 Nov
Substance Class Chemical
Created
by admin
on Tue Mar 06 11:29:20 UTC 2018
Edited
by admin
on Tue Mar 06 11:29:20 UTC 2018
Record UNII
O9FVV27P11
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RIBAVIRIN MONOPHOSPHATE
Common Name English
1H-1,2,4-TRIAZOLE-3-CARBOXAMIDE, 1-(5-O-PHOSPHONO-.BETA.-D-RIBOFURANOSYL)-
Systematic Name English
RIBAVIRIN 5'-MONOPHOSPHATE
Common Name English
NSC-274937
Code English
VIRAZOLE 5'-PHOSPHATE
Common Name English
Code System Code Type Description
PUBCHEM
100252
Created by admin on Tue Mar 06 11:29:20 UTC 2018 , Edited by admin on Tue Mar 06 11:29:20 UTC 2018
PRIMARY SWITZERF
EPA CompTox
40925-28-8
Created by admin on Tue Mar 06 11:29:20 UTC 2018 , Edited by admin on Tue Mar 06 11:29:20 UTC 2018
PRIMARY
CAS
40925-28-8
Created by admin on Tue Mar 06 11:29:20 UTC 2018 , Edited by admin on Tue Mar 06 11:29:20 UTC 2018
PRIMARY
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