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Design, Synthesis and Bioactivity Evaluation of 4,6-Disubstituted Pyrido[3,2-d]pyrimidine Derivatives as Mnk and HDAC Inhibitors.
Xing, Kun; Zhang, Jian; Han, Yu; Tong, Tong; Liu, Dan; Zhao, Linxiang.
  • Xing K; Key Laboratory of Structure-Based Drug Design & Discovery of Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.
  • Zhang J; Key Laboratory of Structure-Based Drug Design & Discovery of Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.
  • Han Y; Key Laboratory of Structure-Based Drug Design & Discovery of Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.
  • Tong T; Key Laboratory of Structure-Based Drug Design & Discovery of Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.
  • Liu D; Key Laboratory of Structure-Based Drug Design & Discovery of Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.
  • Zhao L; Key Laboratory of Structure-Based Drug Design & Discovery of Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.
Molecules ; 25(18)2020 Sep 21.
Article en En | MEDLINE | ID: mdl-32967084
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Pirimidinas / Diseño de Fármacos / Proteínas Serina-Treonina Quinasas / Péptidos y Proteínas de Señalización Intracelular Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Pirimidinas / Diseño de Fármacos / Proteínas Serina-Treonina Quinasas / Péptidos y Proteínas de Señalización Intracelular Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article