GSK1904529A

Binding assays

Kinases were activated by preincubating the enzyme (2.7 μmol/L final concentration) in 50 mmol/L HEPES (pH 7.5), 10 mmol/L MgCl2, 0.1 mg/mL bovine serum albumin, and 2 mmol/L ATP. Compounds were diluted in DMSO and dispensed into the assay plates (100 nL/well). Kinase reactions contained (in 10 μL volume) 50 mmol/L HEPES (pH 7.5), 3 mmol/L DTT, 0.1 mg/mL bovine serum albumin, 1 mmol/L CHAPS, 10 mmol/L MgCl2, 10 μmol/L ATP, 500 nmol/L substrate peptide (biotin-aminohexyl-AEEEEYMMMMAKKKK-NH2; QPC), and 0.5 nmol/L activated enzyme. Reactions were stopped after 1 h at room temperature with 33 μmol/L EDTA. Peptide phosphorylation was measured by time-resolved fluorescence resonance energy transfer with 7 nmol/L streptavidin-Surelight allophycocyanin and 1 nmol/L europium-conjugated phosphotyrosine antibodies. Plates were read in a Victor X5 or ViewLux 1430 ultra HTS microplate imager.

Cell lines

NIH-3T3 cells that overexpress human IGF-IR [NIH-3T3-hIGF-IR (NIH-3T3/LISN)] and IR (NIH-3T3-hIR)

Preparation method

The solubility of this compound in DMSO is >42.6mg/mL. General tips for obtaining a higher concentration: Please warm the tube at 37 ℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months.

Reacting condition

72 h

Applications

In the NIH-3T3/LISN and NIH-3T3-hIR cells, GSK1904529A potently inhibited phosphorylation of IGF-IR and IR with the IC50 of 22 ± 8 nmol/L and 19 ± 8 nmol/L, respectively. GSK1904529A suppressed cell proliferation in a variety of tumor cells with the IC50 values of 81, 35, 43, 124, 137 and 68 nM for NCI-H929, TC-71, SK-N-MC, COLO 205, MCF7 and PREC, respectively. In COLO 205, MCF-7, and NCI-H929 cells, GSK1904529A resulted in cell accumulation in G1 and decrease in S and G2-M phases.

Animal models

Female athymic nu/nu CD-1 mice bearing NIH-3T3/LISN, COLO 205, HT29, and BxPC3 cells

Dosage form

Oral administration, 30 mg/kg, once or twice daily for 21 d

Application

In NIH-3T3/LISN tumor-bearing mice, GSK1904529A (oral, 30 mg/kg, twice-daily) inhibited 98% tumor growth. In COLO 205 xenografts mice, GSK1904529A (oral, 30 mg/kg, once daily) inhibited 75% tumor growth. Among HT29 and BxPC3 xenografts, GSK1904529A produced moderate tumor growth inhibition with no side effects at a dose of 30 mg/kg.

Other notes

Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal.

References:

[1]. Sabbatini P, Rowand J L, Groy A, et al. Antitumor activity of GSK1904529A, a small-molecule inhibitor of the insulin-like growth factor-I receptor tyrosine kinase. Clinical Cancer Research, 2009, 15(9): 3058-3067.