613-92-3,MFCD00031485
Catalog No.:AA003NXR

613-92-3 | N-Hydroxy-benzamidine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$6.00   $4.00
- +
1g
97%
in stock  
$8.00   $6.00
- +
10g
95%
in stock  
$30.00   $21.00
- +
25g
97%
in stock  
$47.00   $33.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003NXR
Chemical Name:
N-Hydroxy-benzamidine
CAS Number:
613-92-3
Molecular Formula:
C7H8N2O
Molecular Weight:
136.1512
MDL Number:
MFCD00031485
SMILES:
O/N=C(/c1ccccc1)\N
NSC Number:
13999
Properties
Properties
 
BP:
307.4°C at 760 mmHg  
Form:
Solid  
MP:
77 °C  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
128  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
1  
Formal Charge:
0  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.1  

Literature

Title: The mitochondrial Amidoxime Reducing Component (mARC) is involved in detoxification of N-hydroxylated base analogues.

Journal: Chemical research in toxicology 20121119

Title: Insight into technetium amidoxime complex: oxo technetium(V) complex of N-substituted benzamidoxime as new basic structure for molecular imaging.

Journal: Inorganic chemistry 20110207

Title: Reduction of N(ω)-hydroxy-L-arginine by the mitochondrial amidoxime reducing component (mARC).

Journal: The Biochemical journal 20110115

Title: Convenient synthesis and biological profile of 5-amino-substituted 1,2,4-oxadiazole derivatives.

Journal: European journal of medicinal chemistry 20101201

Title: A novel and specific fluorescence reaction for uracil.

Journal: Analytica chimica acta 20100803

Title: The fourth molybdenum containing enzyme mARC: cloning and involvement in the activation of N-hydroxylated prodrugs.

Journal: Journal of medicinal chemistry 20081225

Title: Involvement of stearoyl-CoA desaturase in the reduction of amidoxime prodrugs.

Journal: Xenobiotica; the fate of foreign compounds in biological systems 20080901

Title: N,N'-dihydroxyamidines: a new prodrug principle to improve the oral bioavailability of amidines.

Journal: Journal of medicinal chemistry 20071227

Title: Identification of the missing component in the mitochondrial benzamidoxime prodrug-converting system as a novel molybdenum enzyme.

Journal: The Journal of biological chemistry 20061117

Title: Hepatic, extrahepatic, microsomal, and mitochondrial activation of the N-hydroxylated prodrugs benzamidoxime, guanoxabenz, and Ro 48-3656 ([[1-[(2s)-2-[[4-[(hydroxyamino)iminomethyl]benzoyl]amino]-1-oxopropyl]-4-piperidinyl]oxy]-acetic acid).

Journal: Drug metabolism and disposition: the biological fate of chemicals 20051101

Title: Characterization and partial purification of the rat and human enzyme systems active in the reduction of N-hydroxymelagatran and benzamidoxime.

Journal: Drug metabolism and disposition: the biological fate of chemicals 20050401

Title: Metabolism of benzamidoxime (N-hydroxyamidine) in human hepatocytes and role of UDP-glucuronosyltransferases.

Journal: Xenobiotica; the fate of foreign compounds in biological systems 20050101

Title: N-Aryl N'-hydroxyguanidines, a new class of NO-donors after selective oxidation by nitric oxide synthases: structure-activity relationship.

Journal: Journal of medicinal chemistry 20020214

Title: Phase 2 metabolites of N-hydroxylated amidines (amidoximes): synthesis, in vitro formation by pig hepatocytes, and mutagenicity testing.

Journal: Chemical research in toxicology 20010301

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SDS
Tags:613-92-3 Molecular Formula|613-92-3 MDL|613-92-3 SMILES|613-92-3 N-Hydroxy-benzamidine
Catalog No.: AA003NXR
613-92-3,MFCD00031485
613-92-3 | N-Hydroxy-benzamidine
Pack Size: 250mg
Purity: 97%
in stock
$6.00 $4.00
Pack Size: 1g
Purity: 97%
in stock
$8.00 $6.00
Pack Size: 10g
Purity: 95%
in stock
$30.00 $21.00
Pack Size: 25g
Purity: 97%
in stock
$47.00 $33.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA003NXR
Chemical Name: N-Hydroxy-benzamidine
CAS Number: 613-92-3
Molecular Formula: C7H8N2O
Molecular Weight: 136.1512
MDL Number: MFCD00031485
SMILES: O/N=C(/c1ccccc1)\N
NSC Number: 13999
Properties
BP: 307.4°C at 760 mmHg  
Form: Solid  
MP: 77 °C  
Storage: Inert atmosphere;Room Temperature;  
Complexity: 128  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 1  
Formal Charge: 0  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.1  
Literature fold

Title: The mitochondrial Amidoxime Reducing Component (mARC) is involved in detoxification of N-hydroxylated base analogues.

Journal: Chemical research in toxicology20121119

Title: Insight into technetium amidoxime complex: oxo technetium(V) complex of N-substituted benzamidoxime as new basic structure for molecular imaging.

Journal: Inorganic chemistry20110207

Title: Reduction of N(ω)-hydroxy-L-arginine by the mitochondrial amidoxime reducing component (mARC).

Journal: The Biochemical journal20110115

Title: Convenient synthesis and biological profile of 5-amino-substituted 1,2,4-oxadiazole derivatives.

Journal: European journal of medicinal chemistry20101201

Title: A novel and specific fluorescence reaction for uracil.

Journal: Analytica chimica acta20100803

Title: The fourth molybdenum containing enzyme mARC: cloning and involvement in the activation of N-hydroxylated prodrugs.

Journal: Journal of medicinal chemistry20081225

Title: Involvement of stearoyl-CoA desaturase in the reduction of amidoxime prodrugs.

Journal: Xenobiotica; the fate of foreign compounds in biological systems20080901

Title: N,N'-dihydroxyamidines: a new prodrug principle to improve the oral bioavailability of amidines.

Journal: Journal of medicinal chemistry20071227

Title: Identification of the missing component in the mitochondrial benzamidoxime prodrug-converting system as a novel molybdenum enzyme.

Journal: The Journal of biological chemistry20061117

Title: Hepatic, extrahepatic, microsomal, and mitochondrial activation of the N-hydroxylated prodrugs benzamidoxime, guanoxabenz, and Ro 48-3656 ([[1-[(2s)-2-[[4-[(hydroxyamino)iminomethyl]benzoyl]amino]-1-oxopropyl]-4-piperidinyl]oxy]-acetic acid).

Journal: Drug metabolism and disposition: the biological fate of chemicals20051101

Title: Characterization and partial purification of the rat and human enzyme systems active in the reduction of N-hydroxymelagatran and benzamidoxime.

Journal: Drug metabolism and disposition: the biological fate of chemicals20050401

Title: Metabolism of benzamidoxime (N-hydroxyamidine) in human hepatocytes and role of UDP-glucuronosyltransferases.

Journal: Xenobiotica; the fate of foreign compounds in biological systems20050101

Title: N-Aryl N'-hydroxyguanidines, a new class of NO-donors after selective oxidation by nitric oxide synthases: structure-activity relationship.

Journal: Journal of medicinal chemistry20020214

Title: Phase 2 metabolites of N-hydroxylated amidines (amidoximes): synthesis, in vitro formation by pig hepatocytes, and mutagenicity testing.

Journal: Chemical research in toxicology20010301

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