UNC3230

UNC3230

CAT N°: 16401
Price:

From 72.00 61.20

Phosphatidylinositol-4-phosphate 5-kinase type-1 ? (PIP5K1C) is a lipid kinase that generates phosphatidylinositol-4,5-bisphosphate (PIP2) in nociceptive dorsal root ganglia (DRG).{26548} Pain sensitization is regulated by multiple signaling pathways that are initiated by phospholipase C-mediated hydrolysis of PIP2.{26548} UNC3230 is a small molecule inhibitor of PIP5K1C (IC50 = 41 nM, Kd = 51 nM).{26548} It does not inhibit any other lipid kinases that regulate phosphoinositide levels, including phosphatidylinositol 3-kinases.{26548} At 100 nM, UNC3230 decreases PIP2 membrane levels in cultured DRG neurons by 45% and significantly reduces calcium signaling. At 2 nM, it displays antinociceptive effects in mouse models of chronic pain when administered intrathecally or injected into inflamed hindpaw.{26548}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • 5-[(cyclohexylcarbonyl)amino]-2-(phenylamino)-4-thiazolecarboxamide
  • Correlated keywords
    • inhibitors inhibitions inhibits kinases pains signals transductions neurosciences biochemicals UNCs UNC-3230 3230 PIP5K1C phosphatidylinositol 4-phosphate 4 phosphates 5 types 1C calcium signaling antinociceptive anti-nociceptive anti nociceptive effects chronic intrathecally injected inflamed hindpaws analgesic PIP2 4,5-bisphosphate DRG neurons dorsal roots ganglia ?
  • Product Overview:
    Phosphatidylinositol-4-phosphate 5-kinase type-1 ? (PIP5K1C) is a lipid kinase that generates phosphatidylinositol-4,5-bisphosphate (PIP2) in nociceptive dorsal root ganglia (DRG).{26548} Pain sensitization is regulated by multiple signaling pathways that are initiated by phospholipase C-mediated hydrolysis of PIP2.{26548} UNC3230 is a small molecule inhibitor of PIP5K1C (IC50 = 41 nM, Kd = 51 nM).{26548} It does not inhibit any other lipid kinases that regulate phosphoinositide levels, including phosphatidylinositol 3-kinases.{26548} At 100 nM, UNC3230 decreases PIP2 membrane levels in cultured DRG neurons by 45% and significantly reduces calcium signaling. At 2 nM, it displays antinociceptive effects in mouse models of chronic pain when administered intrathecally or injected into inflamed hindpaw.{26548}

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