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Recent progress toward developing axial chirality bioactive compounds.
Wang, Zheyi; Meng, Liying; Liu, Xinxin; Zhang, Lingzi; Yu, Zongjiang; Wu, Guanzhao.
Afiliación
  • Wang Z; Department of Medical Experimental Center, Qilu Hospital (Qingdao), Cheeloo College of Medicine, Shandong University, Qingdao, 266035, China.
  • Meng L; Department of Medical Experimental Center, Qilu Hospital (Qingdao), Cheeloo College of Medicine, Shandong University, Qingdao, 266035, China.
  • Liu X; Department of Medical Experimental Center, Qilu Hospital (Qingdao), Cheeloo College of Medicine, Shandong University, Qingdao, 266035, China.
  • Zhang L; Department of Pharmacy, Qilu Hospital (Qingdao), Cheeloo College of Medicine, Shandong University, Qingdao, 266035, China.
  • Yu Z; CAS Key Laboratory of Bio-based Materials, Qingdao Institute of BioEnergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, 266101, People's Republic of China. Electronic address: yuzj@qibebt.ac.cn.
  • Wu G; Department of Medical Experimental Center, Qilu Hospital (Qingdao), Cheeloo College of Medicine, Shandong University, Qingdao, 266035, China. Electronic address: guanzhao.wu@email.sdu.edu.cn.
Eur J Med Chem ; 243: 114700, 2022 Dec 05.
Article en En | MEDLINE | ID: mdl-36058089
ABSTRACT
Atropisomers are stereoisomers with axial chirality arising from restricted rotation around a single bond. Lots of representatives of this class of axially chiral compounds exhibit remarkable biological properties for protein targets. This time-dependent chirality shows great potential for drug development. Herein, we comprehensively review axial chirality bioactive compounds, including C-C bonded atropisomers, C-N bonded atropisomers, and N-N bonded atropisomers. Examples of each are provided along with their biological activity. This review highlights the development of various examples of atropisomerism encountered in bioactive compounds, which is beneficial for medicinal chemists to advance atropisomeric drug molecules.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estereoisomerismo Idioma: En Revista: Eur J Med Chem Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estereoisomerismo Idioma: En Revista: Eur J Med Chem Año: 2022 Tipo del documento: Article País de afiliación: China
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