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H-1152 . dihydrochloride

ALX-270-423

18 citations

  • ALX-270-423-M001   —   1 mg
    $89.00
  • ALX-270-423-M005   —   5 mg
    $359.00
  • ALX-270-423-M025   —   25 mg
    $1,027.00

A cell permeable, highly specific, potent and ATP-competitive inhibitor of Rho kinase (ROCK) (Ki=1.6nM). Exhibits a much weaker affinity for other serine/threonine kinases (Ki=630nM for PKA, 9.27mM for PKC and 10.1mM for MLCK). More potent and selective than Y-27632 (Prod. No. ALX-270-333). Inhibits the phosphorylation of MARCKS in cells stimulated by lysophosphatidic acid. Inhibits EP3-stimulated NO formation. Prevents fragmentation of apoptotic cells. Relieves neuropathic pain.

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Regulatory Status

RUO – Research Use Only