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Product overview

  • Name
    KN 92
  • Short description
    Reduces Cav1.2 and Cav1.3 channel currents. Inactive analog of KN 93.
  • Biological description
    Reduces Cav1.2 and Cav1.3 channel currents. Inactive analog of KN 93. Inhibits nicotine and potassium stimulation of tyrosine hydroxylase activity. Displays no activity for CAMKII and GLUT4.
  • Biological action
  • Purity
  • Citations


  • Chemical name
  • Molecular Weight
  • Chemical structure
    KN 92  [1135280-28-2]
  • Molecular Formula
  • CAS Number

Storing and Using Your Product

  • Storage instructions
  • Solubility overview
    soluble in DMSO (10mM)
  • Important
    This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.

References for KN 92

  • CaMKII-independent effects of KN93 and its inactive analog KN92: reversible inhibition of L-type calcium channels.

    Gao L et al (2006) Biochem Biophys Res Commun 345(4) : 1606-10.
    PubMedID: 16730662
  • CaMK activation during exercise is required for histone hyperacetylation and MEF2A binding at the MEF2 site on the Glut4 gene.

    Smith JA et al (2008) Am J Physiol Endocrinol Metab 295(3) : E698-704.
    PubMedID: 18647882
  • The Ca++/calmodulin-dependent protein kinase II inhibitors KN62 and KN93, and their inactive analogues KN04 and KN92, inhibit nicotinic activation of tyrosine hydroxylase in bovine chromaffin cells.

    Marley PD et al (1996) Biochem Biophys Res Commun 221(1) : 15-8.
    PubMedID: 8660326
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