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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
Kinetic and structural characterization of caspase-3 and caspase-8 inhibition by a novel class of irreversible inhibitors.
2010-09
Application of matrix solid-phase dispersion to the determination of amitrole and urazole residues in apples by capillary electrophoresis with electrochemical detection.
2008-06
The use of biophysical methods increases success in obtaining liganded crystal structures.
2007-01
Determination of amitrole and urazole in water samples by capillary zone electrophoresis using simultaneous UV and amperometrical detection.
2005-12-16
Three subsets of sequence complexity and their relevance to biopolymeric information.
2005-08-11
Stereocontrolled synthesis of a complex library via elaboration of angular epoxyquinol scaffolds.
2005-08-05
Novel concerted fragmentation upon alcoholysis of a urazole.
2004-10-14
The first method for protection-deprotection of the indole 2,3-pi bond.
2003-05-29
High-throughput synthesis and optimization of thrombin inhibitors via urazole alpha-addition and Michael addition.
2003-04-17
Vibrational frequencies and structural determinations of urazole.
2003-02
Detoxification on top of enhanced, diamine-extended glutaraldehyde fixation significantly reduces bioprosthetic root calcification in the sheep model.
2003-01
The anticalcific effect of glutaraldehyde detoxification on bioprosthetic aortic wall tissue in the sheep model.
2002-04-02
Characterization of the immune response to valve bioprostheses and its role in primary tissue failure.
2001-05
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:54:43 GMT 2025
Edited
by admin
on Mon Mar 31 19:54:43 GMT 2025
Record UNII
U4VGB8C36D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-15394
Preferred Name English
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
3,5-DIKETOTRIAZOLIDINE
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID5062920
Created by admin on Mon Mar 31 19:54:43 GMT 2025 , Edited by admin on Mon Mar 31 19:54:43 GMT 2025
PRIMARY
FDA UNII
U4VGB8C36D
Created by admin on Mon Mar 31 19:54:43 GMT 2025 , Edited by admin on Mon Mar 31 19:54:43 GMT 2025
PRIMARY
MERCK INDEX
m11321
Created by admin on Mon Mar 31 19:54:43 GMT 2025 , Edited by admin on Mon Mar 31 19:54:43 GMT 2025
PRIMARY Merck Index
PUBCHEM
72916
Created by admin on Mon Mar 31 19:54:43 GMT 2025 , Edited by admin on Mon Mar 31 19:54:43 GMT 2025
PRIMARY
MESH
C421465
Created by admin on Mon Mar 31 19:54:43 GMT 2025 , Edited by admin on Mon Mar 31 19:54:43 GMT 2025
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NSC
1892
Created by admin on Mon Mar 31 19:54:43 GMT 2025 , Edited by admin on Mon Mar 31 19:54:43 GMT 2025
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ECHA (EC/EINECS)
221-776-9
Created by admin on Mon Mar 31 19:54:43 GMT 2025 , Edited by admin on Mon Mar 31 19:54:43 GMT 2025
PRIMARY
NSC
15394
Created by admin on Mon Mar 31 19:54:43 GMT 2025 , Edited by admin on Mon Mar 31 19:54:43 GMT 2025
PRIMARY
CAS
3232-84-6
Created by admin on Mon Mar 31 19:54:43 GMT 2025 , Edited by admin on Mon Mar 31 19:54:43 GMT 2025
PRIMARY