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JNJ-54175446 

Cat. No. M28720

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JNJ-54175446  Structure
Size Price Availability Quantity
1mg USD 500  USD500 In stock
5mg USD 800  USD800 In stock
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Quality Control & Documentation
Biological Activity

JNJ-54175446 is a potent and selective brain penetrant P2X7 receptor antagonist, with pIC50s of 8.46 and 8.81 for hP2X7 receptor and rP2X7 receptor, respectively.

Chemical Information
Molecular Weight 440.78
Formula C18H13ClF4N6O
CAS Number 1627902-21-9
Form Solid
Solubility (25°C) DMSO 62.5 mg/mL (ultrasonic)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Kasper Recourt, et al. J Psychopharmacol. Characterisation of the pharmacodynamic effects of the P2X7 receptor antagonist JNJ-54175446 using an oral dexamphetamine challenge model in healthy males in a randomised, double-blind, placebo-controlled, multiple ascending dose trial

[2] Yan Xu, et al. Clin Transl Sci. Translational Model-Informed Dose Selection for a Human Positron Emission Tomography Imaging Study of JNJ-54175446, a P2X7 Receptor Antagonist

[3] Hartmuth C Kolb, et al. J Nucl Med. Preclinical Evaluation and Nonhuman Primate Receptor Occupancy Study of 18F-JNJ-64413739, a PET Radioligand for P2X7 Receptors

[4] Michel Koole, et al. J Nucl Med. 18F-JNJ-64413739, a Novel PET Ligand for the P2X7 Ion Channel: Radiation Dosimetry, Kinetic Modeling, Test-Retest Variability, and Occupancy of the P2X7 Antagonist JNJ-54175446

[5] Maarten Timmers, et al. J Psychopharmacol. Clinical pharmacokinetics, pharmacodynamics, safety, and tolerability of JNJ-54175446, a brain permeable P2X7 antagonist, in a randomised single-ascending dose study in healthy participants

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Keywords: JNJ-54175446  supplier, P2 Receptor, inhibitors, activators

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