Design and Structural Optimization of Methionine Adenosyltransferase 2A (MAT2A) Inhibitors with High In Vivo Potency and Oral Bioavailability

Inhibition of methionine adenosyltransferase 2A (MAT2A) in cancers with a deletion of methylthioadenosine phosphorylase (MTAP) gene leads to synthetic lethality, thus receiving significant interest in the field of precise cancer treatment. Herein, we report the discovery of a tetrahydrobenzo[4,5]imidazo[1,2- a ]pyrazine fragment which occupies the MAT2A allosteric pocket. The lead compound 8 exhibited extremely high potency to inhibit MAT2A enzymatic activity (IC 50 = 18 nM) and proliferation of MTAP-null cancer cells (IC 50 = 52 nM). 8 had a favorable pharmacokinetic profile with a bioavailability of 116% in mice. More importantly, introducing an amide motif ( 28 ) to the core structure raised the plasma drug exposure from 11 718 to 41 192 ng·h·mL –1 . 28 displayed a significantly better in vivo potency than AG-270, which is being evaluated in clinical trails, and induced −52% tumor regression in a xenograft MTAP-depleted colon tumor model.