MSC778 is an effective and orally active flap endonuclease 1 ( FEN1 ) inhibitor with an IC 50 of 3 nM and a K D of 2.9 nM. MSC778 exhibits 145-fold, 516-fold, and 65-fold selectivity over EXO1, GEN1, and XPG, respectively. MSC778 selectively kills BRCA2-deficient cells and potentiates the activity of Niraparib ( HY-10619 ) to induce tumor stasis in a BRCA2 KO DLD-1 mouse xenograft. MSC778 can be used in the research of colorectal cancer .
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