VU0661013

2131184-57-9

C39H39Cl2N5O4

H2O : < 0.1 mg/mL (insoluble); DMSO : >= 125 mg/mL (175.40 mM)

Apoptosis

VU661013 is a potent and selective MCL-1 inhibitor. IC50 & Target: MCL-1^[1] In Vitro: VU661013 exhibits a K_i of 97+/-30 pM to human MCL-1 in a TR-FRET assay by displacing a fluorescently labeled peptide derived from the pro-apoptotic protein BAK. However, VU661013 does not significantly inhibit BCL-xL (K_i>40 uM) or BCL-2 (K_i=0.73 uM)^[1]. In Vivo: VU661013, a novel, potent, selective MCL-1 inhibitor that de-stabilizes BIM/MCL-1 association, leads to apoptosis in AML, and is active in Venetoclax-resistant cells and patient derived xenografts. After establishing disseminated leukemia, NSGS mice are dosed intraperitoneally with 10, 25 or 75 mg/kg of VU661013 daily for 21 days. Weekly chimerism analyses are conducted and the percentage of MV-4-11 cells are quantified in murine peripheral blood using anti-human CD45 (hCD45) and anti-hCD33 monoclonal antibodies. Twenty-eight days post-transplant, vehicle-treated mice have developed large leukemia burdens and thus, mice are sacrificed, and their organs are harvested for analysis. Vehicle mice treated died of xenografted AML, but have no evidence of VU661013-related toxicity in non target organs. VU661013 treatment of disseminated human AML results in a dose-dependent decrease in tumor burden, nearly eliminating the hCD45⁺ MV-4-11 cells at the 75 mg/kg dose in the blood (mean, 13.0+/-2.2% in vehicle vs 7.4+/-7.2% in 25mg/kg vs 0.17+/-0.12% in 75 mg/kg treated mice), bone marrow (mean, 40.7+/-13.9% in vehicle vs 33.46+/-4.0 % in 25 mg/kg vs 0.384+/-0.345 in 75 mg/kg treated mice), and spleen (mean, 46.22+/-13.3% in vehicle vs 13.31+/-10.0% in 25 mg/kg vs 1.588+/-1.51% in 75 mg/kg treated mice). Treatment with VU661013 reduces disease-associated splenomegaly (mean, vehicle vs. 75mg/kg, 0.17+/-0.02 vs 0.09+/-0.01g), and amendeding spleen to body weight ratio (vehicle vs 75mg/kg, 0.99 vs 0.50). In a second MV-4-11 xenograft study, mice are followed until death, and survival is evaluated by Kaplan-Meier analysis. In this study, NSGS mice are treated daily (starting 7 days after transplant) with vehicle only, 15 mg/kg or 75 mg/kg of VU661013. Analysis reveals an increase in survival in mice treated with the 75mg/kg dose (vehicle treated mice=31 days, vs 15 mg/kg=32 days, vs 75 mg/kg treated mice=43 Days)^[1].