Bemcentinib

1037624-75-1

C30H34N8

DMSO : 10.25 mg/mL (20.23 mM; Need ultrasonic and warming)

Protein Tyrosine Kinase/RTK

Bemcentinib (R428) is a potent and selective inhibitor of Axl with an IC₅₀ of 14 nM. IC50 & Target: IC50: 14 nM (Axl kinase) In Vitro: Bemcentinib (R428) (2uM) significantly interferes with mechanisms of migration and invasion of Axlpos melanoma cells at levels comparable to Axl knockdown^[1]. Bemcentinib (R428) synergizes with CDDP to enhance suppression of liver micrometastasis^[2]. Bemcentinib (R428) (50 nM-1uM) causes a concentration-dependent inhibition of preadipocyte differentiation into mature adipocytes, as evidenced by reduced lipid uptake^[3]. In Vivo: Bemcentinib (R428) (125 mg/kg, p.o.) significantly blocks MDA-MB-231-luc-D3H2LN metastases development in two independent mouse models of breast cancer dissemination, suppresses both tumor angiogenesis and vascular endothelial growth factor (VEGF)-induced corneal neovascularization in vivo^[2]. Bemcentinib (R428) (75 mg/kg/day, 25 mg/kg twice daily, p.o.) makes mice keep on a high-fat diet resulted in significantly reduced weight gain and subcutaneous and gonadal fat mass^[3].