Article
Synthesis and Structural Optimization of 2,7,9-Trisubstituted purin-8-ones as FLT3-ITD Inhibitors.
International journal of molecular sciences - 18 Dec 2022
Tomanová Monika, Kozlanská Karolína, Jorda Radek, Jedinák Lukáš, Havlíková Tereza, Řezníčková Eva, Peřina Miroslav, Klener Pavel, Dolníková Alexandra, Cankař Petr, Kryštof Vladimír
Abstract excerpt
Therapy of FLT3-positive acute myeloid leukemia still remains complicated, despite the availability of newly approved kinase inhibitors. Various strategies to avoid the reduced efficacy of therapy have been explored, including the development of dual targeting compounds, which inhibit FLT3 and another kinase necessary for the survival and proliferation of AML cells. We have designed new 2,7,9-trisubstituted...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
