M8891 is an Orally Active and Brain Penetrant MetAP-2 Inhibitor

Removal of N-terminal methionine by methionine aminopeptidases (MetAP) is a crucial step in the maturation of proteins during protein biosynthesis. Besides, MetAP-2 is one of the two cytoplasmic methionine aminopeptidases expressed in mammalian cells. Moreover, MetAP-2 acts as a target of the highly potent and irreversible inhibitor fumagillin to which antiangiogenic and antitumoral properties have been ascribed. These and other findings rationalize the development of MetAP-2 inhibitors for cancer therapy. This and other findings support the rationale to develop MetAP2 inhibitors for cancer therapy. In addition to the fumagillin class of MetAP-2 inhibitors, structurally divergent MetAP-2 inhibitors include substrate-like bestatin class. Furthermore, it also includes modified marine natural products like benzamide class, anthranilic acid sulfonamide analogs, triazole or purine derivatives and others. Structural investigations of this chemical matter revealed divergent interaction patterns. M8891 is an orally active, reversible and brain penetrant Methionine Aminopeptidase-2 inhibitor with antiangiogenic and antitumoral activity.

M8891 is an Orally Active and Brain Penetrant MetAP 2 Inhibitor - M8891 is an Orally Active and Brain Penetrant MetAP-2 Inhibitor

M8891 is an orally active, reversible and brain penetrant Methionine Aminopeptidase-2 (MetAP-2) inhibitor with an IC50 of 54 nM and a Ki of 4.33 nM. In addition, M8891 does not inhibit MetAP-1 (IC50>10 µM). Specifically, M8891 inhibits the growth of primary endothelial cells as well as tumor cells and demonstrates antiangiogenic and antitumoral activity. We observed the accumulation of an unprocessed MetAP2 substrate, methylated elongation factor 1 α, Met-EF1a, upon treatment with M8891. In combination with sunitinib, M8891 demonstrated strong and durable antitumor activity in a cohort of patient-derived renal cancer xenografts at well-tolerated exposure levels. All in all, M8891 is an orally active, reversible and brain penetrant Methionine Aminopeptidase-2 inhibitor with antiangiogenic and antitumoral activity.

References:

 Heinrich T, et al. J Med Chem. 2019 Dec 26;62(24):11119-11134.