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Cat. No. Product Name Information
PC-42954

HG6-64-1

TAK1/MAP4K2 inhibitor

HG6-64-1 is a potent dual TAK1 and MAP4K2 ((germinal center kinase, GCK)) inhibitor with IC50 of 41 nM and 98 nM, respectively.
PC-62937

MAP4K4-IN-44

MAP4K4 inhibitor

MAP4K4-IN-44 is a potent, moderately selective small molecule MAP4K4 inhibitor with IC50 of 5 nM in LC3K assay, demonstrates favorable in vivo bioavailability in mouse.
PC-62936

GNE-220

MAP4K4 inhibitor

GNE-220 is a potent and selective inhibitor of MAP4K4 with IC50 of 7 nM, also inhibits MINK (MAP4K6), DMPK and KHS1 (MAP4K5) with IC50 of 9 nM, 476 nM and 1,110 nM.
PC-62935

MAP4K4-IN-17

MAP4K4 inhibitor

MAP4K4-IN-17 is a potent and highly selective MAP4K4 inhibitor with IC50 of 14.9 nM, showes improved overall drug-like properties compared to PF-06260933.
PC-61694

PF-06260933 dihydrochloride

MAP4K4 inhibitor

PF-06260933 dihydrochloride is a potent, selective and orally bioavailable MAP4K4 inhibitor with kinase IC50 of 3.7 nM, cell IC50 of 160 nM.
PC-61165

MAP4K4-IN-11e

MAP4K4 inhibitor

MAP4K4-IN-11e is a potent, selective, ATP-competitive inhibitor of MAP4K4 with IC50 of 1.9 uM, without effect on other stress pathway related kinases.
PC-60014

PF-06260933

MAP4K4 inhibitor

PF-06260933 (PF06260933,PF6260933) is a potent, selective, orally available MAP4K4 inhibitor with IC50 of 3.7 nM.
PC-42105

GNE-495

MAP4K4 inhibitor

GNE-495 (GNE495) is a potent and highly selective, cell permeable MAP4K4 inhibitor with IC50 of 3.7 nM.
PC-23624

Prostetin-12k

MAP4K inhibitor, MLK3 inhibitor

Prostetin/12k is a highly potent, blood-brain barrier-penetrant inhibitor of mitogen-activated protein kinase kinase kinase kinase (MAP4K) family with IC50 of 0.3 nM for HGK (MAP4K4) and 23.7 nM for MLK3.
PC-23589

PF-07265028

HPK1 inhibitor

PF-07265028 is a potent, selective hematopoietic progenitor kinase 1 (HPK1/MAP4K1) with Ki of <0.05 nM, and cellular IC50 of 17 nM (pSLP76 inhibition).
PC-23066

BGB-15025

HPK1 inhibitor

BGB-15025 is a potent and selective hematopoietic progenitor kinase 1 (HPK1) inhibitor with biochemical IC50 of 1.04 nM.
PC-23064

GNE-6893

HPK1 inhibitor

GNE-6893 is a potent, selective and orally active inhibitor of HPK1 (hematopoietic progenitor kinase 1) with Ki of <0.019 nM, potently inhibits phosphorylation of SLP76 with IC50 of 44 nM in Jurkat cell assay.

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