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Cat. No. Product Name Information
PC-42937

FR 180204

ERK1/2 inhibitor

FR 180204 is a potent, selective, ATP-competitive ERK inhibitor with Ki of 0.31 and 0.14 uM for ERK1 and ERK2, respectively.
PC-62596

MK-8353 hydrochloride

MK-8353 hydrochloride (SCH-900353) is a highly potent, orally bioavailable, dual-specificity ERK1/2 inhibitor with IC50 of 23.0/8.8 nM, respectively.
PC-62595

MK-8353

ERK1/2 inhibitor

MK-8353 (SCH-900353) is a highly potent, orally bioavailable, dual-specificity ERK1/2 inhibitor with IC50 of 23.0/8.8 nM, respectively.
PC-61978

KO-947

ERK1/2 inhibitor

KO-947 (KO947) is a potent and selective inhibitor of ERK1/2 kinase in biochemical, cellular and in vivo antitumor activity assays.
PC-61973

LY3214996

ERK1/2 inhibitor

Temuterkib (LY-3214996) is a novel potent, selective, orally active ERK1/2 inhibitor with IC50 of 5 nM for both enzymes in biochemical assays.
PC-70300

AX-15836

ERK5 inhibitor

AX-15836 (AX15836) is a potent, highly selective ERK5 inhibitor with IC50 of 8 nM.
PC-42663

Pluripotin

ERK1 inhibitor

Pluripotin(SC1) is a small molecule that can maintain the self-renewal of mESC (murine embryonic stem cells) in the absence of feeder cells and exogenous factors.
PC-45562

DEL-22379

ERK dimerization inhibitor

DEL-22379 (DEL22379) is a small molecule inhibitor of ERK dimerization with IC50 of 0.5 uM, without affecting ERK phosphorylation.
PC-43855

VX-11e

ERK2 inhibitor

VX-11e is a potent, selective, and orally bioavailable inhibitor of ERK2 with Ki of <2 nM.
PC-45868

SCH772984

ERK1/2 inhibitor

SCH772984 is a potent and selective inhibitor of ERK1/ERK2 with IC50 of 4 nM/1 nM, respectively.
PC-22330

Ravoxertinib

ERK inhibitor

Ravoxertinib (GDC-0994) is potent, selective and orally active ERK kinase inhibitor with IC50 of 6.1 nM and 3.1 nM for ERK1 and ERK2, respectively.
PC-20223

Ulixertinib hydrochloride

ERK inhibitor

Ulixertinib hydrochloride (BVD-523) is a potent, selective, reversible, ATP-competitive ERK1/2 inhibitor with Ki of 0.3/0.04 nM, respectively.

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