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(+/-)-NFPS HYDROCHLORIDE

Base Information Edit
  • Chemical Name:(+/-)-NFPS HYDROCHLORIDE
  • CAS No.:200006-08-2
  • Molecular Formula:C24H25ClFNO3
  • Molecular Weight:429.91
  • Hs Code.:
  • Mol file:200006-08-2.mol
(+/-)-NFPS HYDROCHLORIDE

Synonyms:ALX 5407 HYDROCHLORIDE;N-[3-(4'-FLUOROPHENYL)-3-(4'-PHENYLPHENOXY)PROPYL]SARCOSINE HYDROCHLORIDE;(±)-NFPS hydrochloride, N-[3-(4μ-Fluorophenyl)-3-(4μ-phenylphenoxy)propyl]sarcosine hydrochloride;

Suppliers and Price of (+/-)-NFPS HYDROCHLORIDE
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • NFPS hydrochloride
  • 5mg
  • $ 420.00
  • TRC
  • ALX 5407 hydrochloride
  • 1mg
  • $ 195.00
  • Tocris
  • ALX 5407 hydrochloride ≥98%(HPLC)
  • 10
  • $ 212.00
  • Sigma-Aldrich
  • ALX 5407 hydrochloride ≥98% (HPLC)
  • 25mg
  • $ 438.00
  • Sigma-Aldrich
  • ALX 5407 hydrochloride ≥98% (HPLC)
  • 5mg
  • $ 111.00
  • Biosynth Carbosynth
  • ALX 5407 hydrochloride
  • 10 mg
  • $ 125.00
  • Biosynth Carbosynth
  • ALX 5407 hydrochloride
  • 50 mg
  • $ 437.50
  • ApexBio Technology
  • ALX 5407 hydrochloride
  • 10mg
  • $ 314.00
  • AK Scientific
  • ALX 5407 hydrochloride
  • 50mg
  • $ 1265.00
Total 27 raw suppliers
Chemical Property of (+/-)-NFPS HYDROCHLORIDE Edit
Chemical Property:
  • PSA:49.77000 
  • LogP:5.82130 
  • Storage Temp.:2-8°C 
  • Solubility.:DMSO: ~16 mg/mL, soluble 
Purity/Quality:

98%,99%, *data from raw suppliers

NFPS hydrochloride *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xn,N 
  • Hazard Codes:Xn,N 
  • Statements: 22-50/53 
  • Safety Statements: 22-24/25-61-60 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses ALX 5407 Hydrochloride can be used in the preparation of amino acid derivatives as pharmaceuticals for treatment of neurological and neuropsychiatric disorders. ALX 5407 hydrochloride has been used as a glycine transporter (GlyT1) inhibitor to test its effect on inhibitory postsynaptic current and N-methyl-D-aspartate receptor (NMDA)-mediated excitatory postsynaptic currents (EPSCs). It has also been used as a GlyT1 inhibitor to treat developmentally diminished NMDA receptor (Grin1D481N) mice to test its effect on the glycine site function.
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