37388-05-9 | (1R,2S)-2-Phenylcyclopropanamine hydrochloride

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	1 week	$143.00	$100.00
250mg	95%	1 week	$218.00	$152.00
2.5g	95%	1 week	$1,765.00	$1,236.00
5g	95%	1 week	$2,575.00	$1,803.00
10g	95%	1 week	$3,781.00	$2,647.00

Description

• Catalog Number: AX16100
• Chemical Name: (1R,2S)-2-Phenylcyclopropanamine hydrochloride
• CAS Number: 37388-05-9
• Molecular Formula: C9H12ClN
• Molecular Weight: 169.65128
• MDL Number: MFCD17976456
• SMILES: N[C@@H]1C[C@H]1c1ccccc1.Cl

Computed Properties

• Complexity: 116
• Covalently-Bonded Unit Count: 2
• Defined Atom Stereocenter Count: 2
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1

Literature

• Low molecular weight amidoximes that act as potent inhibitors of lysine-specific demethylase 1.

  Journal of medicinal chemistry 20120913

• A predictive ligand-based Bayesian model for human drug-induced liver injury.

  Drug metabolism and disposition: the biological fate of chemicals 20101201

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101

• Genetic mapping of targets mediating differential chemical phenotypes in Plasmodium falciparum.

  Nature chemical biology 20091001

• Microsphere-based protease assays and screening application for lethal factor and factor Xa.

  Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

• Fluorinated phenylcyclopropylamines. 2. Effects of aromatic ring substitution and of absolute configuration on inhibition of microbial tyramine oxidase.

  Journal of medicinal chemistry 20041118

• Fluorinated phenylcyclopropylamines. 1. Synthesis and effect of fluorine substitution at the cyclopropane ring on inhibition of microbial tyramine oxidase.

  Journal of medicinal chemistry 20040325