BiochemProbe — Life Science Research Reagents

KN-92 free base · Parent KN-93 · Synonyms: KN92 | KN 92

KN-92 is anKN-92 is an inactive derivative of KN-93, without CaM kinase inhibitory activity.

For research use only. Not for human or veterinary use.

Target CaMK
Area Cancer
Purity >98% Stock In stock

Description

KN-92 is anKN-92 is an inactive derivative of KN-93, without CaM kinase inhibitory activity. KN-92 is intended to be used as a control compound in studies designed to elucidate the antagonist activities of KN-93. KN-93 is a cell-permeable, reversible and competitive CaMKII inhibitor[1][2]. inactive derivative of KN-93, without CaM kinase inhibitory activity.

Biological activity

KN-93 (5-50 μM; 24 hours) inhibits LX-2 cell growth and KN-92 (5-50 μM; 24 hours) is ineffective in blocking cell growth[2]. The analysis of cell cycle regulator expression reveals that KN-93 rather than KN-92 reduces the expression of p53 and p21[2].

Identifiers

SMILES
COC1=CC=C(C=C1)S(=O)(=O)NC1=CC=CC=C1CN(C)C\C=C\C1=CC=C(Cl)C=C1

Specifications

MW (average)
456.9850
Formula
C24H25ClN2O3S
CAS No.
176708-42-2
Physical state
Solid
Color
White to off-white
Shipping
Room temperature in continental US; may vary elsewhere.
Storage
Powder -20°C 3 years; 4°C 2 years; In solvent -80°C 6 months; -20°C 1 month

References

[1]. Smyth JT, et al. Inhibition of the inositol trisphosphate receptor of mouse eggs and A7r5 cells by KN-93 via a mechanism unrelated to Ca2+/calmodulin-dependent protein kinase II antagonism. J Biol Chem. 2002;277(38):35061-35070.
[2]. An P, et al. KN-93, a specific inhibitor of CaMKII inhibits human hepatic stellate cell proliferation in vitro. World J Gastroenterol. 2007;13(9):1445-1448.