White solid. PROTECT FROM LIGHT. Useful general cell-permeable protein kinase inhibitor. Potent inhibitor of CaM kinase II (Ki = 1.8 nM). Also inhibits myosin light chain kinase (Ki = 17 nM), protein kinase A (Ki = 18 nM), protein kinase C (Ki = 25 nM), and protein kinase G (Ki = 20 nM). Acts as a potent inhibitor (IC50 = 3 nM) of the protein tyrosine kinase activity of the NGF receptor gp140trk as well as the kinase activity of its transforming alleles, the trk oncogenes, and of the related neurotrophin receptors gp145trkB and gp145trkC. Induces apoptosis and cell cycle arrest by inhibiting Cdk1 and Cdc25c. IC50 = 35 nM for Flt3 autophosphorylation in Flt3/Itd-BaF3 cells. Purity: ≥95% by HPLC. RTECS NZ0550000, CAS 97161-97-2. Ref.: Cools, J., et al. 2004. Cancer Res. 64, 6385. Chin, L.S., et al. 1999. Cancer Invest. 17, 391. Nakanishi, N., et al. 1995. FEBS Lett. 368, 411. Ross, A.H., et al. 1995. J. Neurochem. 65, 2748. Mizuno, K., et al. 1993. FEBS Lett. 330, 114. Pawlowska, Z., et al. 1993. J. Neurochem. 60, 678. Tapley, P., et al. 1992. Oncogene 7, 371. Simpson, D.L., et al. 1991. J. Neurosci. Res. 28, 486. Hashimoto, S. 1988. J. Cell Biol. 107, 1531. Koizuma, S, et al. 1988. J. Neurosci. 8, 715. Kase, H., et al. 1987. Biochem. Biophys. Res. Commun. 142, 436. |