PK11195

PK11195 Structure
PK11195 structure
Common Name PK11195
CAS Number 85532-75-8 Molecular Weight 352.857
Density 1.2±0.1 g/cm3 Boiling Point 511.7±45.0 °C at 760 mmHg
Molecular Formula C21H21ClN2O Melting Point 74-75
MSDS Chinese USA Flash Point 263.3±28.7 °C

Inhibitory action of 1-(2-chlorophenyl)-N-methyl-N-(1-methylpropyl)-3-isoquinolinecarboxam ide (PK 11195) on some mononuclear phagocyte functions.

Biochem. Pharmacol. 59 , 1305-1314, (2000)

Peripheral benzodiazepine receptors (PBRs) are widely distributed throughout the body, but their functions are unknown. They are found on mononuclear phagocytes, and they are up-regulated in a number of neurological and other disease states. We explored the f...

Chronic exposure of rat primary astrocyte cultures to manganese results in increased binding sites for the 'peripheral-type' benzodiazepine receptor ligand 3H-PK 11195.

Neurosci. Lett. 271 , 5, (1999)

Alterations of 'peripheral-type' benzodiazepine receptors (PTBRs) in brain are a feature of hepatic encephalopathy (HE). Although ammonia toxicity has been implicated in the disorder, recent findings suggest an accumulation of manganese in the brains of cirrh...

Pharmacokinetics of the peripheral benzodiazepine receptor antagonist, PK 11195, in rats. The effect of dose and gender.

Pharmacol. Res. 41 , 461-468, (2000)

In spite of the extensive use of the peripheral benzodiazepine (BZ) receptor antagonist, PK 11195 (PK), in pharmacological studies, there is a lack of information of its pharmacokinetics in the rat. In this study the pharmacokinetics of PK were determined aft...

Inhibitory regulation of amylase release in rat parotid acinar cells by benzodiazepine receptors.

Eur. J. Pharmacol. 359 , 243-249, (1998)

This study examined the influence of benzodiazepine receptors on amylase release from rat parotid acinar cells. Diazepam (10(-8)-10(-6) M), which is a potent agonist of both central- and peripheral-type benzodiazepine receptors, dose dependently decreased amy...