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Cat. No. Product Name Information
PC-20222

Ulixertinib

ERK inhibitor

BVD-523 (Ulixertinib) is a potent, selective, reversible, ATP-competitive ERK1/2 inhibitor with Ki of 0.3/0.04 nM, respectively.
PC-38371

Rineterkib

ERK1/2 inhibitor

Rineterkib (LTT-462) is a small molecule inhibitor of ERK1/2, has demonstrated preclinical activity in multiple MAPK activated cancer cells and xenograft models.
PC-72428

ASN007

ERK inhibitor

ASN007 (ASN-007) is a potent, selective, orally bioavailable ERK1/2 inhibitor with IC50 of 2 nM against both.
PC-72401

ASTX029

ERK1/2 inhibitor

ASTX029 (ASTX-029) is a highly potent, selective dual-mechanism ERK inhibitor with IC50 of <3 nM for ERK1/2, inhibits both ERK catalytic activity and the phosphorylation of ERK by MEK.
PC-72142

XMD8-85

ERK5 inhibitor

XMD8-85 is a selective ERK5 inhibitor with IC50 of 87 nM in enzyme assay.
PC-72141

JWG-071

ERK5 inhibitor

JWG-071 is a selective Erk5 inhibitor (IC50<20 nM) with reduced Brd4/BET inhibitory activity.
PC-72106

SF-3-030

ERK1/2 inhibitor

SF-3-030 is a novel ATP-dependent/catalytic site inhibitor of ERK1/2, inhibits A375 cell viability with IC50 of 4.9 uM.
PC-35813

CC-90003

ERK1/2 inhibitor

CC-90003 (CC90003) is a potent and selective, covalent ERK1/2 inhibitor with IC50 of 10-20 nM, demonstrates excellent selectivity in a 258-kinase biochemical assay panel.
PC-35338

AZ6197

ERK1/2 inhibitor

AZ6197 (AZ-6197) is a potent, selective, reversible inhibitor of ERK1/2 with IC50 of <0.3 nM (ERK2), inhibits pERK/pRSK with IC50 of 12/62 nM in A375 cells, respectively.
PC-35332

BAY885

ERK5 inhibitor

BAY-885 (BAY885) is a highly potent, selective ERK5 (MAPK7) inhibitor with IC50 of 40 nM, shows high selectivity over a panel of 357 kinases (Eurofins panel).
PC-63537

Astex ERK inhibitor X

ERK1/2 inhibitor

Astex ERK inhibitor X (ERK inhibitor 29) is a potent, selective ERK1/2 inhibitor that inhibits ERK catalytic activity with IC50 of 3 nM.
PC-63271

AZD0364

ERK1/2 inhibitor

Tizaterkib (AZD0364) is a potent, selective, ATP competitive, orally active ERK1/2 inhibitor with IC50 of 0.66 nM in ERK2 biochemical assay, binds similarly to ERK1 and ERK2 with Ki of 3.9 and 3.8 nM.

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