C0424

PK 11195

• Synonym(e): 1-(2-Chlorophenyl)-N-methyl-N-(1-methylpropyl)-3-isoquinolinecarboxamide
• Empirische Formel (Hill-System): C₂₁H₂₁ClN₂O
• CAS-Nummer: 85532-75-8
• Molekulargewicht: 352.86
• MDL-Nummer: MFCD00069334
• UNSPSC-Code: 12352200
• PubChem Substanz-ID: 24278822
• NACRES: NA.77

Eigenschaften

• Form: powder
• Qualitätsniveau: 200
• SMILES String: 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
• InChIKey: RAVIZVQZGXBOQO-UHFFFAOYSA-N
• Angaben zum Gen: human ... BZRAP1(9256) , TSPO(706) ; rat ... Gabra2(29706) , Tspo(24230)

Beschreibung

Anwendung

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.

Biochem./physiol. Wirkung

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.

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable