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Description: DT-061 (also known as SMAP) is a novel, potent and orally bioavailable activator of PP2A (protein phosphatase 2A). It could be applied in the therapy of KRAS-mutant and MYC-driven tumorigenesis. Treatment with DT-061, in combination with the MEK inhibitor AZD6244, resulted in suppression of both p-AKT and MYC, as well as tumor regression in two KRAS-driven lung cancer mouse models. DT-061 therapy also abrogated MYC-driven tumorigenesis.
References: Sci Transl Med. 2018 Jul 18; 10(450). pii: eaaq1093.
Related CAS : 1809427-19-7; 1809427-18-6 (1S, 2S, 3R isomer)
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