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Chem Biodivers ; 21(2): e202301584, 2024 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-38163253

RESUMO

XY153 is a promising BET BD2 inhibitor with an IC50 value of 0.79 nM against BRD4 BD2. It shows 354-fold selectivity over BRD4-BD1 and 6-fold selectivity over other BET BD2 domains. However, the reported synthesis route of XY153 and its derivatives are extremely poor-yielding. After the synthesis of three key fragments, XY153 can only be obtained with a yield of 1.3 % in the original four-step reaction. In this study, we reported a three-step alternative route in the synthesis process of XY153. The reaction conditions for this route were thoroughly investigated and optimized, resulting in a significantly improved yield of 61.5 %. This efficient synthesis route establishes a robust chemical foundation for the rapid synthesis of XY153 derivatives as BET BD2 inhibitors in the near future.


Assuntos
Antineoplásicos , Fatores de Transcrição , Fatores de Transcrição/química , Proteínas Nucleares/química , Proteínas de Ciclo Celular
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