C0424

PK 11195

• Sinónimos: 1-(2-Chlorophenyl)-N-methyl-N-(1-methylpropyl)-3-isoquinolinecarboxamide
• Fórmula empírica (notación de Hill): C₂₁H₂₁ClN₂O
• Número de CAS: 85532-75-8
• Peso molecular: 352.86
• Número MDL: MFCD00069334
• Código UNSPSC: 12352200
• ID de la sustancia en PubChem: 24278822
• NACRES: NA.77

Propiedades

• Formulario: powder
• Nivel de calidad: 200
• cadena SMILES: CCC(C)N(C)C(=O)c1cc2ccccc2c(n1)-c3ccccc3Cl
• InChI: 1S/C21H21ClN2O/c1-4-14(2)24(3)21(25)19-13-15-9-5-6-10-16(15)20(23-19)17-11-7-8-12-18(17)22/h5-14H,4H2,1-3H3
• Clave InChI: RAVIZVQZGXBOQO-UHFFFAOYSA-N
• Información sobre el gen: human ... BZRAP1(9256) , TSPO(706) ; rat ... Gabra2(29706) , Tspo(24230)

Descripción

Aplicación

PK 11195 has been used as an inhibitor of peripheral benzodiazepine receptor (PBR) homologs in primitive erythrocytes of embryos and in osteosarcoma cytoplasmic hydrids. It has also been used as an unlabelled competitive binder in in vitro autoradiography experiments in cardiac tissue sections.

Acciones bioquímicas o fisiológicas

PK 11195 is a peripheral benzodiazepine antagonist. It is also an antagonist for human constitutive androstane receptor (hCAR) and human pregnane X receptor (PXR). In human primary hepatocytes, PK 11195 upon demethylation elicits agonist functionality towards the receptor hCAR. PK 11195 also antagonise B-cell lymphoma 2 (Bcl-2) and may serve as a potential compound for mitochondrial targeting therapies and in the treatment of cholangiocarcinoma.

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable