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Details

Stereochemistry ABSOLUTE
Molecular Formula C8H11N3O6
Molecular Weight 245.1894
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 6-AZAURIDINE

SMILES

OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N2N=CC(=O)NC2=O

InChI

InChIKey=WYXSYVWAUAUWLD-SHUUEZRQSA-N
InChI=1S/C8H11N3O6/c12-2-3-5(14)6(15)7(17-3)11-8(16)10-4(13)1-9-11/h1,3,5-7,12,14-15H,2H2,(H,10,13,16)/t3-,5-,6-,7-/m1/s1

HIDE SMILES / InChI

Molecular Formula C8H11N3O6
Molecular Weight 245.1894
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
6-Azauridine in combination chemotherapy of childhood acute myelocytic leukemia.
1972 Apr
Inhibitory effect of selected antiviral compounds on measles (SSPE) virus replication in vitro.
1989 Sep
Inhibition of sandfly fever Sicilian virus (Phlebovirus) replication in vitro by antiviral compounds.
1997 Sep-Oct
Antiviral activity and mode of action studies of ribavirin and mycophenolic acid against orthopoxviruses in vitro.
2001 Nov
Site specific incorporation of 6-azauridine into the genomic HDV ribozyme active site.
2001 Oct-Nov
Comparison of colorimetric, fluorometric, and visual methods for determining anti-influenza (H1N1 and H3N2) virus activities and toxicities of compounds.
2002 Oct
Use of nucleotide analogs by class I and class II CCA-adding enzymes (tRNA nucleotidyltransferase): deciphering the basis for nucleotide selection.
2003 Aug
Glycyrrhizin, an active component of liquorice roots, and replication of SARS-associated coronavirus.
2003 Jun 14
Interferon, ribavirin, 6-azauridine and glycyrrhizin: antiviral compounds active against pathogenic flaviviruses.
2003 Mar
A simple assay for determining antiviral activity against Crimean-Congo hemorrhagic fever virus.
2004 Apr
Comprehensive analysis of risk factors associating with Hepatitis B virus (HBV) reactivation in cancer patients undergoing cytotoxic chemotherapy.
2004 Apr 5
In vitro inhibition of Chikungunya and Semliki Forest viruses replication by antiviral compounds: synergistic effect of interferon-alpha and ribavirin combination.
2004 Feb
[Biotechnological synthesis of ribavirin. Effect of ribavirin and its various combinations on the reproduction of Vaccinia virus].
2004 Nov-Dec
Synthesis of N3-substituted uridine and related pyrimidine nucleosides and their antinociceptive effects in mice.
2005 Mar
Broad-spectrum inhibitor of viruses in the Flaviviridae family.
2005 Nov
Azacytidine (Vidaza(R)) in the treatment of myelodysplastic syndromes.
2006 Dec
6-Azauracil or 8-aza-7-deazaadenine nucleosides and oligonucleotides: the effect of 2'-fluoro substituents and nucleobase nitrogens on conformation and base pairing.
2008 Feb 7
Structure and inhibition of orotidine 5'-monophosphate decarboxylase from Plasmodium falciparum.
2008 Mar 25
N-methylisatin-beta-thiosemicarbazone derivative (SCH 16) is an inhibitor of Japanese encephalitis virus infection in vitro and in vivo.
2008 May 22
Antimicrobial and cytotoxic arylazoenamines. Part III: antiviral activity of selected classes of arylazoenamines.
2008 Sep 15
Antiviral activity of indole derivatives.
2009 Aug
Transcript elongation factor TFIIS is involved in arabidopsis seed dormancy.
2009 Feb 27
Antiviral and cytotoxic activities of aminoarylazo compounds and aryltriazene derivatives.
2009 Jul 1
Hepatoprotective Activity of Licorice Water Extract against Cadmium-induced Toxicity in Rats.
2009 Jun
Recognition of acyl donors by lipase CAL-B in the acylation of 6-azauridine.
2009 May-Jun
Insights into arbovirus evolution and adaptation from experimental studies.
2010 Dec
Six RNA viruses and forty-one hosts: viral small RNAs and modulation of small RNA repertoires in vertebrate and invertebrate systems.
2010 Feb 12
Historical perspectives in the development of antiviral agents against poxviruses.
2010 Jun
Triplet formation of 6-azauridine and singlet oxygen sensitization with UV light irradiation.
2010 May 21
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:07:40 GMT 2023
Edited
by admin
on Fri Dec 15 15:07:40 GMT 2023
Record UNII
7BVB29RCPR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
6-AZAURIDINE
HSDB   MI  
Systematic Name English
6-AZAURACIL RIBOSIDE
Common Name English
6-AZAURIDINE [HSDB]
Common Name English
6-AZAURIDINE [MI]
Common Name English
6-AZAURACIL-.BETA.-D-RIBOSIDE
Common Name English
AZAURIDINE
MART.  
Systematic Name English
NSC-32074
Code English
RIBOAZAURACIL
Common Name English
AZAURIDINE [MART.]
Common Name English
6-AZUR
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C2170
Created by admin on Fri Dec 15 15:07:40 GMT 2023 , Edited by admin on Fri Dec 15 15:07:40 GMT 2023
NCI_THESAURUS C1557
Created by admin on Fri Dec 15 15:07:40 GMT 2023 , Edited by admin on Fri Dec 15 15:07:40 GMT 2023
Code System Code Type Description
CHEBI
35668
Created by admin on Fri Dec 15 15:07:40 GMT 2023 , Edited by admin on Fri Dec 15 15:07:40 GMT 2023
PRIMARY
NSC
32074
Created by admin on Fri Dec 15 15:07:40 GMT 2023 , Edited by admin on Fri Dec 15 15:07:40 GMT 2023
PRIMARY
ECHA (EC/EINECS)
200-199-6
Created by admin on Fri Dec 15 15:07:40 GMT 2023 , Edited by admin on Fri Dec 15 15:07:40 GMT 2023
PRIMARY
FDA UNII
7BVB29RCPR
Created by admin on Fri Dec 15 15:07:40 GMT 2023 , Edited by admin on Fri Dec 15 15:07:40 GMT 2023
PRIMARY
NCI_THESAURUS
C291
Created by admin on Fri Dec 15 15:07:40 GMT 2023 , Edited by admin on Fri Dec 15 15:07:40 GMT 2023
PRIMARY
EVMPD
SUB197079
Created by admin on Fri Dec 15 15:07:40 GMT 2023 , Edited by admin on Fri Dec 15 15:07:40 GMT 2023
PRIMARY
SMS_ID
100000182789
Created by admin on Fri Dec 15 15:07:40 GMT 2023 , Edited by admin on Fri Dec 15 15:07:40 GMT 2023
PRIMARY
HSDB
3206
Created by admin on Fri Dec 15 15:07:40 GMT 2023 , Edited by admin on Fri Dec 15 15:07:40 GMT 2023
PRIMARY
MERCK INDEX
m2167
Created by admin on Fri Dec 15 15:07:40 GMT 2023 , Edited by admin on Fri Dec 15 15:07:40 GMT 2023
PRIMARY Merck Index
PUBCHEM
5901
Created by admin on Fri Dec 15 15:07:40 GMT 2023 , Edited by admin on Fri Dec 15 15:07:40 GMT 2023
PRIMARY
MESH
D001380
Created by admin on Fri Dec 15 15:07:40 GMT 2023 , Edited by admin on Fri Dec 15 15:07:40 GMT 2023
PRIMARY
CAS
54-25-1
Created by admin on Fri Dec 15 15:07:40 GMT 2023 , Edited by admin on Fri Dec 15 15:07:40 GMT 2023
PRIMARY
EPA CompTox
DTXSID20960091
Created by admin on Fri Dec 15 15:07:40 GMT 2023 , Edited by admin on Fri Dec 15 15:07:40 GMT 2023
PRIMARY