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Details

Stereochemistry ABSOLUTE
Molecular Formula C8H13N4O8P
Molecular Weight 324.1849
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RIBAVIRIN 5'-PHOSPHATE

SMILES

C([C@]1([H])[C@]([H])([C@]([H])([C@]([H])(n2cnc(C(=O)N)n2)O1)O)O)OP(=O)(O)O

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 324.1849
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
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 Sat Jun 26 03:34:40 UTC 2021
Edited
by admin
on Sat Jun 26 03:34:40 UTC 2021
Record UNII
O9FVV27P11
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RIBAVIRIN 5'-PHOSPHATE
Common Name English
1H-1,2,4-TRIAZOLE-3-CARBOXAMIDE, 1-(5-O-PHOSPHONO-.BETA.-D-RIBOFURANOSYL)-
Systematic Name English
RIBAVIRIN MONOPHOSPHATE
Common 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 Sat Jun 26 03:34:40 UTC 2021 , Edited by admin on Sat Jun 26 03:34:40 UTC 2021
PRIMARY
EPA CompTox
40925-28-8
Created by admin on Sat Jun 26 03:34:40 UTC 2021 , Edited by admin on Sat Jun 26 03:34:40 UTC 2021
PRIMARY
DRUG BANK
DB14663
Created by admin on Sat Jun 26 03:34:40 UTC 2021 , Edited by admin on Sat Jun 26 03:34:40 UTC 2021
PRIMARY
CAS
40925-28-8
Created by admin on Sat Jun 26 03:34:40 UTC 2021 , Edited by admin on Sat Jun 26 03:34:40 UTC 2021
PRIMARY
FDA UNII
O9FVV27P11
Created by admin on Sat Jun 26 03:34:40 UTC 2021 , Edited by admin on Sat Jun 26 03:34:40 UTC 2021
PRIMARY
Related Record Type Details
PARENT -> METABOLITE
BY adenosine kinase