PF 750 structure
|
Common Name | PF 750 | ||
---|---|---|---|---|
CAS Number | 959151-50-9 | Molecular Weight | 345.438 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 582.7±32.0 °C at 760 mmHg | |
Molecular Formula | C22H23N3O | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 306.2±25.1 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of PF 750PF 750 is a selective and covalent fatty acid amide hydrolase (FAAH) inhibitor, with IC50s varied from 16.2-595 nM in different pre-incubation times. Covalently modifies the enzyme’s active site serine nucleophile[1]. |
Name | N-phenyl-4-(quinolin-3-ylmethyl)piperidine-1-carboxamide |
---|---|
Synonym | More Synonyms |
Description | PF 750 is a selective and covalent fatty acid amide hydrolase (FAAH) inhibitor, with IC50s varied from 16.2-595 nM in different pre-incubation times. Covalently modifies the enzyme’s active site serine nucleophile[1]. |
---|---|
Related Catalog | |
Target |
IC50: 16.2-595 nM (FAAH)[1]. |
References |
Density | 1.2±0.1 g/cm3 |
---|---|
Boiling Point | 582.7±32.0 °C at 760 mmHg |
Molecular Formula | C22H23N3O |
Molecular Weight | 345.438 |
Flash Point | 306.2±25.1 °C |
Exact Mass | 345.184113 |
PSA | 45.23000 |
LogP | 3.77 |
Vapour Pressure | 0.0±1.6 mmHg at 25°C |
Index of Refraction | 1.672 |
N-Phenyl-4-(3-quinolinylmethyl)-1-piperidinecarboxamide |
1-Piperidinecarboxamide, N-phenyl-4-(3-quinolinylmethyl)- |
N-Phenyl-4-(quinolin-3-ylmethyl)piperidine-1-carboxamide |
PF-750 |
Nisoxetine hydrochloride |