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Request The Product List ofTAM Receptor (Tyro3-Axl-Mer) TAM Receptor (Tyro3-Axl-Mer)

Cat. No. Product Name Information
PC-20336

R428

Axl inhibitor

R428 (Bemcentinib, BGB324) is potent, selective and orally bioavailable inhibitor of Axl kinase with IC50 of 14 nM.
PC-20335

UNC2881

Mer inhibitor

UNC2881 (UNC-2881) is a potent selective Mer kinase inhibitor with IC50 of 4.3 nM, 84-fold selectivity over Axl and 58-fold over Tyro3.
PC-20334

NPS-1034

MET-AXL inhibitor

NPS-1034 (NPS1034) is a potent, dual MET and AXL inhibitor with IC50 of 48 and 10.3 nM, respectively.
PC-20023

Adrixetinib

Axl/Mer inhibitor

Adrixetinib is a small molecule inhibitor of Axl/Mer RTK.
PC-49565

R992

Mer inhibitor

R992 (MERTK inhibitor) is a novel potent, selective and orally bioavailable inhibitor of Mer tyrosine kinase (MerTK) with IC50 of 18 nM in ADP-Glo assays.
PC-49059

MRX-2843

Mer inhibitor

MRX-2843 (UNC2371) is a potent, selective, orally available ATP-competitive type 1 inhibitor of both Mer and Flt3 with IC50 of 1.3 and 1.0 nM, respectively.
PC-73130

ONO-7475

Axl inhibitor

ONO-7475 (Tamnorzatinib) is a potent inhibitor of the TAM receptor tyrosine kinase family (Axl IC50=0.7 nM), inhibits the phosphorylation of AXL and Mer, suppresses the growth of AML with FLT3 mutations.
PC-72649

UNC5293

MER inhibitor

UNC5293 (UNC-5293) is a potent, highly selective, orally available inhibitor of MER receptor tyrosine kinase (MERTK) with IC50 0.9 nM, Ki 0.19 nM.
PC-72618

PF-07265807

Axl/Mer inhibitor

PF-07265807 (PF 07265807) is a potent, selective dual Axl/Mer inhibitor with IC50 of 6.1 nM, 13.2 nM and 21.6 nM for AXL, MER and TYRO3, respectively.
PC-72617

AZ14145845

Axl/Mer inhibitor

AZ14145845 (Dual Axl-Mer inhibitor 32) is a potent, selective dual Axl/Mer inhibitor with pIC50 of 7.0/7.8.
PC-72446

KRCT-6j

TYRO3 inhibitor

KRCT-6j is a potent and selective TYRO3 inhibitor, 300-fold selectivity for TYRO3 over both AXL and MerTK.
PC-72371

UNC2250

Mer inhibitor

UNC2250 is a potent, selective Mer tyrosine kinase (MerTK) inhibitor with IC50 of 1.7 nM, displays >100-fold selectivity over Axland Tyro3.

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