Chemical Name:N-Phenyl-4-(3-quinolinylmethyl)-1-piperidinecarboxamide
Purity: ≥98% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Irreversible fatty acid amide hydrolase (FAAH) inhibitor (IC50 = 16.2 nM) that displays no activity at a range of other serine hydrolases. Selectively inhibits FAAH within the central nervous system. Orally active.
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Technical Data
M. Wt
345.44
Formula
C22H23N3O
Storage
Store at RT
Purity
≥98% (HPLC)
CAS Number
959151-50-9
PubChem ID
25154868
InChI Key
BIODYGOZWZNCAG-UHFFFAOYSA-N
Smiles
O=C(NC4=CC=CC=C4)N(CC3)CCC3CC2=CC1=CC=CC=C1N=C2
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent
Max Conc. mg/mL
Max Conc. mM
Solubility
DMSO
34.54
100
ethanol
34.54
100
Preparing Stock Solutions
The following data is based on the product molecular weight 345.44. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
2.89 mL
14.47 mL
28.95 mL
5 mM
0.58 mL
2.89 mL
5.79 mL
10 mM
0.29 mL
1.45 mL
2.89 mL
50 mM
0.06 mL
0.29 mL
0.58 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products' biological activity.
Ahnet al (2007) Novel mechanistic class of fatty acid amide hydrolase inhibitors with remarkable selectivity. Biochemistry 46 13019 PMID: 17949010
Mileniet al (2008) Structure-guided inhibitor design for human FAAH by interspecies active site conversion. Proc.Natl.Acad.Sci.USA 105 12820 PMID: