Substance

ID:73221

Names and Identifiers
IUPAC name
N-{3-[5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluorophenyl}propane-1-sulfonamide
IUPAC Traditional name
N-{3-[5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluorophenyl}propane-1-sulfonamide
Synonyms
R7204RG7204RO5185426PLX-4032
Registration numbers
CAS Number
Properties
Product Information
Salt Data
Free Base
Pharmacology Properties
Target
B-Raf
Physical Property
Solubility
DMSO
Safety Information
Storage Condition
-20°C
Molecule Details
Research Area
Description
Malignant melanoma,Colorectal cancer
Protocol
Kinase Assay [1]
RAF kinase activity measurements
The kinase activities of wild-type RAF and mutants are determined by measuring phosphorylation of biotinylated-BAD protein. For each enzyme (0.01 ng), 20 μL reactions are carried out in 20 mM Hepes (pH 7.0), 10 mM MgCl2, 1 mM DTT, 0.01% (v/v) Tween-20, 50 nM biotin-BAD protein, and 1 mM ATP at room temperature. Reactions are stopped at 5 min with 5 μL of a solution containing 20 mM Hepes (pH 7.0), 200 mM NaCl, 80 mM EDTA, 0.3% (w/v) bovine serum albumin (BSA). The stop solution also includes phospho-BAD (Ser112) antibody, streptavidin-coated donor beads, and protein A acceptor beads. The antibody and beads are pre-incubated in stop solution in the dark at room temperature for 30 min. The final dilution of antibody is 1/2000 and the final concentration of each bead is 10 μg/mL. The assay plates are incubated at room temperature for one hour and then are read on a PerkinElmer AlphaQuest reader. Mutant activities are the average of two different batches of purified protein assayed in duplicate in three different experiments.
Cell Assay [2]
Cell Lines
MALME-3M, Colo829, Colo38, A375, SK-MEL28, and A2058 cells
Concentrations
0–10 μM , dissolved in DMSO
Incubation Time
5 days
Methods
Cellular proliferation is evaluated by MTT assay. Briefly, cells are plated in 96-well microtiter plates at a density of 1000 to 5000 cells per well in a volume of 180 μL. PLX4032 is prepared at 10 times the final assay concentration in media containing 1% DMSO. Twenty-four hours after cell plating, 20 μL of the appropriate dilution of PLX4032 are added to plates in duplicate. The plates are assayed for proliferation 6 days after the cells are plated. Percent inhibition is calculated and the IC50 is determined from the regression of a plot of the logarithm of the concentration versus percent inhibition.
Animal Study [2]
Animal Models
Mice (athymic nude) xenograft models of LOX, Colo829, and A375 cells
Formulation
Formulated as microprecipitated bulk powder (MBP), suspended at the desired concentration in an aqueous vehicle containing 2% Klucel LF, and adjusted to pH 4 with dilute HCl
Doses
12.5 mg/kg–100 mg/kg
Administration
Oral gavage twice daily
Molecular Spectra
No Data Available
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References
• Kumar A, et al. J Mol Biol, 2005, 348(1), 183-193.
• Yang H, et al. Cancer Res, 2010, 70(13), 5518-5527.
• Prahallad A, et al. Nature, 2012, 483(7387), 100-103.
• Bollag G, et al. Nature, 2010, 467(7315), 596-599.