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Chembiochem ; 24(1): e202200553, 2023 01 03.
Artigo em Inglês | MEDLINE | ID: mdl-36300584

RESUMO

The transcription factors STAT5a and STAT5b are constitutively active in many human tumors. Combined inhibition of both STAT5 proteins is a valuable approach with promising applications in tumor biology. We recently reported resorcinol bisphosphate as a moderately active inhibitor of the protein-protein interaction domains, the SH2 domains, of both STAT5a and STAT5b. Here, we describe the development of resorcinol bisphosphate to Stafiba, a phosphatase-stable inhibitor of STAT5a and STAT5b with activity in the low micromolar concentration range. Our data provide insights into the structure-activity relationships of resorcinol bisphosphates and the corresponding bisphosphonates for use as inhibitors of both STAT5a and STAT5b.


Assuntos
Resorcinóis , Fator de Transcrição STAT5 , Humanos , Domínios e Motivos de Interação entre Proteínas , Domínios de Homologia de src
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