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MK-8033 

Cat. No. M27598

All AbMole products are for research use only, cannot be used for human consumption.

MK-8033  Structure

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Quality Control & Documentation
Biological Activity

MK-8033 is an orally active ATP competitive c-Met/Ron dual inhibitor (IC50s: 1 nM (c-Met),7 nM (Ron)), with preferential binding to the activated kinase conformation. MK-8033 can be used in the research of cancers, such as breast and bladder cancers, non-small cell lung cancers (NSCLCs).

Chemical Information
Molecular Weight 471.53
Formula C25H21N5O3S
CAS Number 1001917-37-8
Form Solid
Solubility (25°C) DMSO ≥ 46 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Vicki L Keedy, et al. Invest New Drugs. First-in-human phase I dose escalation study of MK-8033 in patients with advanced solid tumors

[2] Nikita V Chukanov, et al. Acta Crystallogr B Struct Sci Cryst Eng Mater. Crystal structure of the OH-dominant gadolinite-(Y) analogue (Y,Ca)2(Fe,□)Be2Si2O8(OH,O)2 from Heftetjern pegmatite, Norway

[3] Chandrani Chattopadhyay, et al. PLoS One. Simultaneous inhibition of the HGF/MET and Erk1/2 pathways affect uveal melanoma cell growth and migration

[4] Alan B Northrup, et al. J Med Chem. Discovery of 1-[3-(1-methyl-1H-pyrazol-4-yl)-5-oxo-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-7-yl]-N-(pyridin-2-ylmethyl)methanesulfonamide (MK-8033): A Specific c-Met/Ron dual kinase inhibitor with preferential affinity for the activated state of c-Met

[5] Vikas Bhardwaj, et al. J Thorac Oncol. C-Met inhibitor MK-8003 radiosensitizes c-Met-expressing non-small-cell lung cancer cells with radiation-induced c-Met-expression

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  Catalog
Abmole Inhibitor Catalog




Keywords: MK-8033  supplier, c-Met, inhibitors, activators

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