Table 5. Characterization of Cellular Activity, Permeability, Efflux, and Metabolic Stability of Compounds 28 and 29.


Inhibition of PRMT5 determined by an SDMA in-cell western assay in the HAP1 MTAP-isogenic cell line pair following compound treatment for 24 h.
Viability growth inhibition assessed after 7 days of compound treatment using a CellTiter-Glo luminescence-based assay in the same HAP1 MTAP-isogenic cells.
MDCKII-WT A–B (10–6 cm/s).
MDCKII-Mdr1 cells (A–B)/(B–A).
Human liver microsomes, Clint, μL/min/mg.