Your browser doesn't support javascript.
loading
Design, synthesis and evaluation of some 1,6-disubstituted-1H-benzo[d]imidazoles derivatives targeted PI3K as anticancer agents.
Ding, Huai-Wei; Yu, Lu; Bai, Meng-Xuan; Qin, Xiao-Chun; Song, Man-Tong; Zhao, Qing-Chun.
Afiliación
  • Ding HW; Key Laboratory of Structure-Based Drug Design and Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.
  • Yu L; School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, China.
  • Bai MX; Key Laboratory of Structure-Based Drug Design and Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.
  • Qin XC; School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, China.
  • Song MT; School of Public Health, Shenyang Medical College, Shenyang 110034, China. Electronic address: songmtong@163.com.
  • Zhao QC; School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, China. Electronic address: zhaoqingchun1967@163.com.
Bioorg Chem ; 93: 103283, 2019 12.
Article en En | MEDLINE | ID: mdl-31585260

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fosfatidilinositol 3-Quinasas / Inhibidores de las Quinasa Fosfoinosítidos-3 / Imidazoles / Antineoplásicos Límite: Humans Idioma: En Revista: Bioorg Chem Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fosfatidilinositol 3-Quinasas / Inhibidores de las Quinasa Fosfoinosítidos-3 / Imidazoles / Antineoplásicos Límite: Humans Idioma: En Revista: Bioorg Chem Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos