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Medchemexpress LLC JNJ-55308942 | 2166558-11-6 | 99.9% | 425.32 | C17H12F5N7O | 5MG
SDP

Catalog No. 5000235465
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JNJ-55308942 is a selective, brain-penetrant P2X7 receptor antagonist supplied for research use. It shows high affinity for human and rat P2X7 channels and includes solubility and formulation guidance to support both in vitro and in vivo studies.

  • Selective P2X7 antagonist with hP2X7 IC50 = 10 nM and rP2X7 IC50 = 15 nM.
  • Brain-penetrant, suitable for central nervous system studies.
  • Molecular formula C17H12F5N7O; molecular weight 425.32.
  • High purity (≈99.9%).
  • Soluble in DMSO (100 mg/mL); in vivo formulations ≥4 mg/mL reported.
  • Supplied in small milligram pack sizes for research applications.

Catalog No. 50-002-35465 Supplier Medchemexpress LLC Supplier No. HY1238575MG
May include imposed supplier surcharges.
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JNJ-55308942 is a selective, brain-penetrant P2X7 receptor antagonist supplied for research use. It shows high affinity for human and rat P2X7 channels and includes solubility and formulation guidance to support both in vitro and in vivo studies.

  • Selective P2X7 antagonist with hP2X7 IC50 = 10 nM and rP2X7 IC50 = 15 nM.
  • Brain-penetrant, suitable for central nervous system studies.
  • Molecular formula C17H12F5N7O; molecular weight 425.32.
  • High purity (≈99.9%).
  • Soluble in DMSO (100 mg/mL); in vivo formulations ≥4 mg/mL reported.
  • Supplied in small milligram pack sizes for research applications.

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