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Details

Stereochemistry ACHIRAL
Molecular Formula C2H3N3O2
Molecular Weight 101.0641
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of URAZOLE

SMILES

O=C1NNC(=O)N1

InChI

InChIKey=UDATXMIGEVPXTR-UHFFFAOYSA-N
InChI=1S/C2H3N3O2/c6-1-3-2(7)5-4-1/h(H3,3,4,5,6,7)

HIDE SMILES / InChI

Molecular Formula C2H3N3O2
Molecular Weight 101.0641
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Characterization of the immune response to valve bioprostheses and its role in primary tissue failure.
2001 May
The anticalcific effect of glutaraldehyde detoxification on bioprosthetic aortic wall tissue in the sheep model.
2001 Nov-Dec
High-throughput synthesis and optimization of thrombin inhibitors via urazole alpha-addition and Michael addition.
2003 Apr 17
Vibrational frequencies and structural determinations of urazole.
2003 Feb
Detoxification on top of enhanced, diamine-extended glutaraldehyde fixation significantly reduces bioprosthetic root calcification in the sheep model.
2003 Jan
The first method for protection-deprotection of the indole 2,3-pi bond.
2003 May 29
Novel concerted fragmentation upon alcoholysis of a urazole.
2004 Oct 14
Three subsets of sequence complexity and their relevance to biopolymeric information.
2005 Aug 11
Stereocontrolled synthesis of a complex library via elaboration of angular epoxyquinol scaffolds.
2005 Aug 5
Determination of amitrole and urazole in water samples by capillary zone electrophoresis using simultaneous UV and amperometrical detection.
2005 Dec 16
The use of biophysical methods increases success in obtaining liganded crystal structures.
2007 Jan
Application of matrix solid-phase dispersion to the determination of amitrole and urazole residues in apples by capillary electrophoresis with electrochemical detection.
2008 Jun
Kinetic and structural characterization of caspase-3 and caspase-8 inhibition by a novel class of irreversible inhibitors.
2010 Sep
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:43:07 GMT 2023
Edited
by admin
on Fri Dec 15 19:43:07 GMT 2023
Record UNII
U4VGB8C36D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
URAZOLE
MI  
Systematic Name English
1,2,4-TRIAZOLIDINE-3,5-DIONE
Systematic Name English
URAZOLE [MI]
Common Name English
NSC-1892
Code English
BICARBAMIMIDE
Systematic Name English
1H-1,2,4-TRIAZOLE-3,5(2H,4H)-DIONE
Systematic Name English
NSC-15394
Code English
3,5-DIKETOTRIAZOLIDINE
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID5062920
Created by admin on Fri Dec 15 19:43:07 GMT 2023 , Edited by admin on Fri Dec 15 19:43:07 GMT 2023
PRIMARY
FDA UNII
U4VGB8C36D
Created by admin on Fri Dec 15 19:43:07 GMT 2023 , Edited by admin on Fri Dec 15 19:43:07 GMT 2023
PRIMARY
MERCK INDEX
m11321
Created by admin on Fri Dec 15 19:43:07 GMT 2023 , Edited by admin on Fri Dec 15 19:43:07 GMT 2023
PRIMARY Merck Index
PUBCHEM
72916
Created by admin on Fri Dec 15 19:43:07 GMT 2023 , Edited by admin on Fri Dec 15 19:43:07 GMT 2023
PRIMARY
MESH
C421465
Created by admin on Fri Dec 15 19:43:07 GMT 2023 , Edited by admin on Fri Dec 15 19:43:07 GMT 2023
PRIMARY
NSC
1892
Created by admin on Fri Dec 15 19:43:07 GMT 2023 , Edited by admin on Fri Dec 15 19:43:07 GMT 2023
PRIMARY
ECHA (EC/EINECS)
221-776-9
Created by admin on Fri Dec 15 19:43:07 GMT 2023 , Edited by admin on Fri Dec 15 19:43:07 GMT 2023
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NSC
15394
Created by admin on Fri Dec 15 19:43:07 GMT 2023 , Edited by admin on Fri Dec 15 19:43:07 GMT 2023
PRIMARY
CAS
3232-84-6
Created by admin on Fri Dec 15 19:43:07 GMT 2023 , Edited by admin on Fri Dec 15 19:43:07 GMT 2023
PRIMARY