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Cat. No. Product Name Information
PC-20332

INCB081776

AXL/MER inhibitor

INCB081776 is a potent and selective dual inhibitor of AXL and MERTK with IC50 of 16 and 14 nM respectively, 30-fold selectivity over TYRO3.
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-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 inhibitor with IC50 of 1.7 nM, displays >100-fold selectivity over Axland Tyro3.
PC-50012

S49076 hydrochloride

S49076 hydrochloride is a potent, ATP-competitive tyrosine kinase inhibitor of MET, AXL/MER, and FGFR1/2/3 with IC50 of <20 nM, also potently inhibits the kinase activity of mutated isoforms of MET (D1246N, Y1248D, Y1248H) and FGFR1/2.
PC-42994

UNC2025 hydrochloride

UNC2025 is a potent, orally bioavailable Mer/FLT3 dual inhibitor with IC50 of 0.74/0.8 nM, 700-fold less active against Met compared to Mer.
PC-61780

TAM-IN-1

TAM-IN-1 is a highly potent, macrocyclic inhibitor of Mer and Axl with Ki of <50 pM and 130 pM, respectively..
PC-61325

N-butylidenephthalide

A natural compound derived from Angelica sinensis that inhibits malignant brain tumor growth in vitro and in vivo.
PC-45668

Glesatinib hydrochloride

Glesatinib (MGCD-265) is a tyrosine kinase inhibitor that potently and selectively inhibits Met and Axl kinase..

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