65884-46-0,MFCD00868966
Catalog No.:AA00FDJO

65884-46-0 | ciadox

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10mg
98%
2 weeks  
$402.00   $282.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00FDJO
Chemical Name:
ciadox
CAS Number:
65884-46-0
Molecular Formula:
C12H9N5O3
Molecular Weight:
271.2316
MDL Number:
MFCD00868966
SMILES:
N#CCC(=O)N/N=C/c1c[n+]([O-])c2c([n+]1[O-])cccc2
Properties
Computed Properties
 
Complexity:
432  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
1  
Formal Charge:
0  
Heavy Atom Count:
20  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-1.3  

Literature

Title: High risk of adrenal toxicity of N1-desoxy quinoxaline 1,4-dioxide derivatives and the protection of oligomeric proanthocyanidins (OPC) in the inhibition of the expression of aldosterone synthetase in H295R cells.

Journal: Toxicology 20160203

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Tags:65884-46-0 Molecular Formula|65884-46-0 MDL|65884-46-0 SMILES|65884-46-0 ciadox
Catalog No.: AA00FDJO
65884-46-0,MFCD00868966
65884-46-0 | ciadox
Pack Size: 10mg
Purity: 98%
2 weeks
$402.00 $282.00
Quantity
- +
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Technical Information
Catalog Number: AA00FDJO
Chemical Name: ciadox
CAS Number: 65884-46-0
Molecular Formula: C12H9N5O3
Molecular Weight: 271.2316
MDL Number: MFCD00868966
SMILES: N#CCC(=O)N/N=C/c1c[n+]([O-])c2c([n+]1[O-])cccc2
Properties
Complexity: 432  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 1  
Formal Charge: 0  
Heavy Atom Count: 20  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -1.3  
Literature fold

Title: High risk of adrenal toxicity of N1-desoxy quinoxaline 1,4-dioxide derivatives and the protection of oligomeric proanthocyanidins (OPC) in the inhibition of the expression of aldosterone synthetase in H295R cells.

Journal: Toxicology20160203

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