Details
Stereochemistry | ACHIRAL |
Molecular Formula | C22H23N3O |
Molecular Weight | 345.4375 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C(NC1=CC=CC=C1)N2CCC(CC3=CC4=CC=CC=C4N=C3)CC2
InChI
InChIKey=BIODYGOZWZNCAG-UHFFFAOYSA-N
InChI=1S/C22H23N3O/c26-22(24-20-7-2-1-3-8-20)25-12-10-17(11-13-25)14-18-15-19-6-4-5-9-21(19)23-16-18/h1-9,15-17H,10-14H2,(H,24,26)
Molecular Formula | C22H23N3O |
Molecular Weight | 345.4375 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/17949010
Sources: https://www.ncbi.nlm.nih.gov/pubmed/17949010
PF-750 is a covalent irreversible inhibitor of FAAH, discovered by Pfizer.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2243 Sources: https://www.ncbi.nlm.nih.gov/pubmed/17949010 |
16.2 nM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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PubMed
Title | Date | PubMed |
---|---|---|
A second fatty acid amide hydrolase with variable distribution among placental mammals. | 2006 Dec 1 |
|
Novel mechanistic class of fatty acid amide hydrolase inhibitors with remarkable selectivity. | 2007 Nov 13 |
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SAR and LC/MS studies of β-lactamic inhibitors of human fatty acid amide hydrolase (hFAAH): evidence of a nonhydrolytic process. | 2011 Oct 13 |
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Covalent inhibitors of fatty acid amide hydrolase: a rationale for the activity of piperidine and piperazine aryl ureas. | 2011 Oct 13 |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/17949010
FAAH activity was measured by following the production of ammonia generated from the hydrolysis of oleamide by FAAH. GDH catalyzes the condensation of ammonia and R-ketoglutarate to glutamate with a concomitant conversion of NADH to nicotinamide adenine dinucleotide, oxidized form (NAD+), which is spectrophotometrically measured at 340 nm. To determine IC50, the reactions were carried out in 96-well clear polystyrene plates in a total volume of 200 uL. To a reaction mixture (140 uL) containing NaPi, pH 7.4, NADH, R-ketoglutarate, ADP, EDTA, and GDH to final concentrations of 50 mM, 150 uM, 3 mM, 2 mM, 1 mM, and 7.5 unit/mL, respectively, was added 20 uL of PF-750 dissolved in 50% DMSO (20 uL of 50% DMSO for controls). After the resulting mixture was mixed in a plate vortex, 20 uL of hFAAH (370 ng) in 20 mM NaPi, pH 7.8/1% Triton X-100, was added and mixed. After this mixture was preincubated at RT for the indicated period of time (5-60 min), the reaction was initiated by addition of 20 uL of 500 uM oleamide dissolved in 25% DMSO and 75% EtOH.The reactions were incubated at 30 °C, and the absorbance at 340 nm was collected over a period of 30 min. IC50 for PF-750 was time-dependend, and varied from 0.595 uM at 5 min pre-incubation to 0.0162 uM at 60 min pre-incubation
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:12:08 GMT 2023
by
admin
on
Sat Dec 16 08:12:08 GMT 2023
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Record UNII |
7756CPP14K
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Record Status |
Validated (UNII)
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Record Version |
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