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Bioorg Med Chem Lett ; 21(21): 6389-92, 2011 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-21930380

RESUMO

As the best-characterized ubiquitin-like protein (UBL), small ubiquitin-related modifier (SUMO) was found to conjugate with a number of proteins to regulate cellular functions including transcription, signal transduction, and cell cycle. While E1, E2 and E3 ligases are responsible for the forward SUMOylation reaction, SUMO-specific proteases (SENPs) reversibly remove SUMO from the SUMOylated proteins. Recently, SENP1 was found to be a potential therapeutic target for the treatment of prostate cancers, but the design and synthesis of its inhibitors have not been reported. We designed and synthesized a series of benzodiazepine-based SENP1 inhibitors, and they showed inhibitory activity as good as IC(50)=9.2µM (compound 38). The structure-activity relationship was also discussed.


Assuntos
Desenho de Fármacos , Inibidores de Proteases/síntese química , Inibidores de Proteases/farmacologia , Proteínas Modificadoras Pequenas Relacionadas à Ubiquitina/metabolismo , Linhagem Celular Tumoral , Avaliação Pré-Clínica de Medicamentos , Eletroforese em Gel de Poliacrilamida , Humanos , Ligação de Hidrogênio , Concentração Inibidora 50 , Modelos Moleculares , Inibidores de Proteases/química
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