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. |