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PK14105 

Cat. No. M27751

All AbMole products are for research use only, cannot be used for human consumption.

PK14105  Structure

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Quality Control & Documentation
Biological Activity

PK14105 is a biological evaluation as a potential radioligand for PET studies of PBBS receptors. in vivo binding experiments, in which PK 14105 was injected into rats with unilaterally lesioned striata, demonstrate that PK 14105 rapidly crosses the blood-brain-barrier and that there is a marked retention of radioactivity in the lesioned striatum not seen in the unlesioned striatum or cerebellar vermis. It can also inhibit receptor ligands, calcium channel ligands and co-transporter in all salivary glands.

Chemical Information
Molecular Weight 381.4
Formula C21H20FN3O3
CAS Number 107257-28-3
Form Solid
Solubility (25°C) DMSO ≥ 30 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Franklin C Wong, et al. Biomed Res Int. Affinity labeling of membrane receptors using tissue-penetrating radiations

[2] H Yamagishi, et al. Jpn J Pharmacol. Pharmacological characterization of an 18-kDa protein associated with the peripheral-type benzodiazepine receptor in salivary glands

[3] G W Price, et al. J Neurochem. In vivo binding to peripheral benzodiazepine binding sites in lesioned rat brain: comparison between [3H]PK11195 and [18F]PK14105 as markers for neuronal damage

[4] D A Cox, et al. J Pharmacol Exp Ther. Identification of a 17-kDa protein associated with the peripheral-type benzodiazepine receptor in vascular and other smooth muscle types

[5] M W McEnery. J Bioenerg Biomembr. The mitochondrial benzodiazepine receptor: evidence for association with the voltage-dependent anion channel (VDAC)

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  Catalog
Abmole Inhibitor Catalog




Keywords: PK14105  supplier, inhibitors, activators

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