124-42-5 | Acetamidine hydrochloride

Packsize	Purity	Availability	Price	Discounted Price
25g	92%	in stock	$11.00	$8.00
100g	92%	in stock	$20.00	$14.00
500g	92%	in stock	$24.00	$17.00

Description

• Catalog Number: AA27491
• Chemical Name: Acetamidine hydrochloride
• CAS Number: 124-42-5
• Molecular Formula: C2H7ClN2
• Molecular Weight: 94.5434
• MDL Number: MFCD00013016
• SMILES: CC(=N)N.Cl
• NSC Number: 7595

Computed Properties

• Complexity: 31
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 5
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 3

Literature

• Novel aminobenzyl-acetamidine derivative modulate the differential regulation of NOSs in LPS induced inflammatory response: role of PI3K/Akt pathway.

  Biochimica et biophysica acta 20121201

• Selective inhibition of inducible nitric oxide synthase by derivatives of acetamidine.

  Medicinal chemistry (Shariqah (United Arab Emirates)) 20121101

• A mild liquid reduction route toward uniform blue-emitting EuCl2 nanoprisms and nanorods.

  Inorganic chemistry 20110801

• Selective inhibition of iNOS by benzyl- and dibenzyl derivatives of N-(3-aminobenzyl)acetamidine.

  ChemMedChem 20110704

• A synthesis of acetamidines.

  The Journal of organic chemistry 20110318

• Characterization and inactivation of an agmatine deiminase from Helicobacter pylori.

  Bioorganic chemistry 20100401

• Haloacetamidine-based inactivators of protein arginine deiminase 4 (PAD4): evidence that general acid catalysis promotes efficient inactivation.

  Chembiochem : a European journal of chemical biology 20100125

• Four-component synthesis of fully substituted 1,2,4-triazoles.

  Angewandte Chemie (International ed. in English) 20100101

• Highly efficient copper-catalyzed cascade synthesis of quinazoline and quinazolinone derivatives.

  Chemical communications (Cambridge, England) 20081221

• Differential effects of selective and non-selective inhibition of nitric oxide synthase on the expression and activity of cyclooxygenase-2 during gastric ulcer healing.

  European journal of pharmacology 20060501