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Cat. No. Product Name Information
PC-72695

MEK4 inhibitor 6ff

MEK4 inhibitor

MEK4 inhibitor 6ff is potent, selective MEK4 inhibitor with IC50 of 66 nM.
PC-72692

MEK4 inhibitor 15o

MEK4 inhibitor

MEK4 inhibitor 15o is potent, selective, cell permeable MEK4 inhibitor with IC50 of 83 nM.
PC-72689

MEK4 inhibitor 10e

MEK4 inhibitor

MEK4 inhibitor 10e is potent, selective cell permeable MEK4 inhibitor with IC50 of 61 nM.
PC-38277

BSJ-04-122

MKK4/7 inhibitor

BSJ-04-122 is a potent, selective, covalent dual MKK4/7 inhibitor with IC50 of 4/181 nM, displays excellent kinome selectivity.
PC-36064

MMK7 inhibitor 4a

MKK7 inhibitor

MMK7 inhibitor 4a is a potent, sepecific, covalent inhibitor of MMK7 with IC50 of 10 nM, displays >800-fold selectivity over EGFR-WT and EGFR-L858R/T790M.
PC-35805

MKK7-COV-9

MKK7 inhibitor

MKK7-COV-9 (MKK7 Covalen inhibitor 9) is a potent, selective, covalent MKK7 inhibitor, displays >1,000-fold selectivity over MKK4.
PC-35804

MKK7-COV-13

MKK7 inhibitor

MKK7-COV-13 (MKK7 Covalent inhibitor 13) is a potent, selective, covalent MKK7 inhibitor with in vitro IC50 of 10 nM, displays >1,000-fold selectivity over MKK4 (IC50>10 uM).
PC-35803

MKK7-COV-3

MKK7 inhibitor

MKK7-COV-3 (MKK7 Covalent inhibitor 3) is a potent, selective, covalent MKK7 inhibitor with in vitro IC50 of 5 nM, displays >1,000-fold selectivity over MKK4 (IC50=7.81 uM).
PC-43541

TAK-733

MEK inhibitor

TAK-733 (TAK733,TAK 733) is a potent, selective, allosteric inhibitor of MEK with IC50 of 3.2 nM (MEK1).
PC-43380

Cobimetinib R-enantiomer

Cobimetinib R-enantiomer (GDC-0973, XL518) is the R-enantiomer of Cobimetinib (GDC-0973, XL518), which is a potent, highly selective inhibitor of mitogen-activated protein kinase kinase(MEK1/2).
PC-43369

Cobimetinib

MEK inhibitor

Cobimetinib (GDC-0973, XL518) is a potent, selective MEK inhibitor with IC50 of 4.2 nM for MEK1.
PC-42877

PD318088

MEK1/2 inhibitor

PD318088 is a potent, non-ATP competitive, allosteric MEK1/2 inhibitor, binds simultaneously with ATP in a region of the MEK1 active site that is adjacent to the ATP-binding site.

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