JH-RE-06, a potent REV1-REV7 interface inhibitor ( IC 50 =0.78 μM; K d =0.42 μM), targets REV1 that interacts with the REV7 subunit of POLζ. JH-RE-06 disrupts mutagenic translesion synthesis (TLS) by preventing recruitment of mutagenic POLζ. JH-RE-06 improves chemotherapy.
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