PK 11195

PK 11195
Names
IUPAC name
N-Butan-2-yl-1-(2-chlorophenyl)-N-methylisoquinoline-3-carboxamide
Other names
PK 11195
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
UNII
  • 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 ☒N
    Key: RAVIZVQZGXBOQO-UHFFFAOYSA-N ☒N
  • CCC(C)N(C)C(=O)c3cc1ccccc1c(n3)-c2ccccc2Cl
Properties
C21H21ClN2O
Molar mass 352.856 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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PK 11195 is an isoquinoline carboxamide which binds selectively to the peripheral benzodiazepine receptor (PBR) (also known as the mitochondrial 18 kDa translocator protein or TSPO). It is one of the most commonly used PBR ligands due to its high affinity for the PBR in all species,[1] although it is starting to be replaced by newer and more selective ligands.[2]

Early autoradiographic studies using tritiated PK 11195 ([3H]PK 11195) demonstrated that in the central nervous system (CNS) of rodents, it binds primarily to the ependymal walls, choroid plexus, and olfactory bulb. However, there is a robust and widespread increase in [3H]PK 11195 binding in the injured nervous system. The binding sites have since been determined to be on glial cells, including microglia, astrocytes, and infiltrating macrophages. The binding of [3H]PK 11195 is considered to be a useful tool in the assessment of neuronal damage.[3][4]

In addition to being a marker of neuronal damage in animal models of CNS damage, PK 11195 has been used successfully with human brain imaging techniques. (R)-[11C]PK 11195 has been used in positron emission tomography (PET) scanning to visualize brain inflammation in patients with neuronal damage. Increases in (R)-[11C]PK 11195 binding have been reported in patients with stroke, traumatic brain injury[5] and in patients with chronic neurodegenerative conditions including Huntington's disease and Parkinson's disease.[6][7]

The first high-resolution 3D solution structure of mammalian (mouse) translocator protein (TSPO) in a complex with its diagnostic PK 11195 ligand was determined by using NMR spectroscopy techniques by scientists from the Max-Planck Institute for Biophysical Chemistry in Goettingen in Germany in March 2014[8] and has a PDB id: 2MGY. The complex stoichiometry was found to be 1 : 1 as the one consistent set of 1H ligand resonances was found with the NOE contacts to five transmembrane helices (TM) in the upper cytosolic part of the protein channel. Residues involved in the ligand binding having direct NOE contacts with the ligand were identified and are as follows A23, V26, L49, V26, A50, I52, W107, L114, A147, L150. These residues are wrapped around the PK 11195 ligand forming a stable hydrophobic binding pocket that can also be regarded as the complex's hydrophobic core. The mammalian TSPO in a complex with diagnostic ligand is monomeric.

The loop located in between TM1 and TM2 helices closes the entrance to the space between helices in which are bound with PK 11195 molecule. Site-directed mutagenesis studies of mTSPO revealed that region important for PK 11195 binding comprise amino acids from 41 to 51, because the deletion of this region resulted in the decrease in PK 11195 binding.[9]

References

[edit]
  1. ^ Pike VW, Halldin C, Crouzel C, Barré L, Nutt DJ, Osman S, Shah F, Turton DR, Waters SL (May 1993). "Radioligands for PET studies of central benzodiazepine receptors and PK (peripheral benzodiazepine) binding sites--current status". Nuclear Medicine and Biology. 20 (4): 503–25. doi:10.1016/0969-8051(93)90082-6. PMID 8389223.
  2. ^ Doorduin J, de Vries EF, Dierckx RA, Klein HC (2008). "PET imaging of the peripheral benzodiazepine receptor: monitoring disease progression and therapy response in neurodegenerative disorders". Current Pharmaceutical Design. 14 (31): 3297–315. doi:10.2174/138161208786549443. PMID 19075709.
  3. ^ Cagnin A, Gerhard A, Banati RB (December 2002). "In vivo imaging of neuroinflammation". European Neuropsychopharmacology. 12 (6): 581–6. doi:10.1016/s0924-977x(02)00107-4. PMID 12468021. S2CID 35085112.
  4. ^ Weissman BA, Raveh L (February 2003). "Peripheral benzodiazepine receptors: on mice and human brain imaging". Journal of Neurochemistry. 84 (3): 432–7. doi:10.1046/j.1471-4159.2003.01568.x. PMID 12558962. S2CID 38106157.
  5. ^ Folkersma H, Boellaard R, Yaqub M, Kloet RW, Windhorst AD, Lammertsma AA, Vandertop WP, van Berckel BN (2011). "Widespread and prolonged increase in (R)-(11)C-PK 11195 binding after traumatic brain injury". J Nucl Med. 52 (8): 1235–9. doi:10.2967/JNUMED.110.084061. PMID 21764792.
  6. ^ Tai YF, Pavese N, Gerhard A, Tabrizi SJ, Barker RA, Brooks DJ, Piccini P (April 2007). "Imaging microglial activation in Huntington's disease". Brain Research Bulletin. 72 (2–3): 148–51. doi:10.1016/j.brainresbull.2006.10.029. PMID 17352938. S2CID 6395304.
  7. ^ Bartels AL, Leenders KL (October 2007). "Neuroinflammation in the pathophysiology of Parkinson's disease: evidence from animal models to human in vivo studies with [11C]PK 11195 PET". Movement Disorders. 22 (13): 1852–6. doi:10.1002/mds.21552. PMID 17592621.
  8. ^ L. Jaremko, M. Jaremko, K. Giller, S. Becker, M. Zweckstetter, Structure of the mitochondrial translocator protein in complex with a diagnostic ligand, Science, 343 (2014) 1363-1366
  9. ^ J. Fan, P. Lindemann, M.G. Feuilloley, V. Papadopoulos, Structural and functional evolution of the translocator protein (18 kDa), Curr Mol Med, 12 (2012) 369-386
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