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PK 11195
- No solubility data
- MF: C21H21ClN2O
- MW: 352.86
Description
PK 11195 is a high-affinity ligand of the translocator protein 18 kDa (TSPO), historically known as the peripheral benzodiazepine receptor.
TSPO is localized mainly to the outer mitochondrial membrane and is widely used as a marker and pharmacological target in neuroinflammation, glial activation and mitochondrial function studies. PK 11195 remains a key reference compound for TSPO binding assays and imaging-related research.
Key Features
- High-affinity TSPO/PBR ligand
- Reference compound for peripheral benzodiazepine receptor studies
- Relevant to mitochondrial and neuroinflammation pharmacology
- Useful comparator for TSPO imaging ligand development
Applications
- TSPO binding and displacement assays
- Neuroinflammation and microglial activation studies
- Mitochondrial pharmacology research
- Radioligand and PET tracer precursor workflows
Related Axon Medchem products include the active isomer (R)-(-)-PK 11195 (Axon 2785), N-Desmethyl-PK 11195 (Axon 2833) and (R)-(-)-N-Desmethyl-PK 11195 (Axon 2784).
More Information
| Parent CAS No. | 85532-75-8 |
|---|---|
| Chemical Name | 1-(2-Chloro-phenyl)-isoquinoline-3-carboxylic acid sec-butyl-methyl-amide |
| SMILES | C1C=C2C=C(C(=O)N(C)C(C)CC)N=C(C3C(Cl)=CC=CC=3)C2=CC=1 |
| MFCD | MFCD00069334 |
| InChi | 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 |
| CID | 1345 |
| Short Description | BZD antagonist |
References
- A Klegeris et al. Inhibitory action of 1-(2-chlorophenyl)-N-methyl-N-(1-methylpropyl)-3-isoquinolinecarboxamide (PK 11195) on some mononuclear phagocyte functions. Biochem. Pharmacol. 2000, 59, 1305-1314.
- EP Wala et al. Pharmacokinetics of the peripheral benzodiazepine receptor antagonist, PK 11195, in rats. The effect of dose and gender. Pharmacol. Res. 2000, 41, 461-468.
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