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Tricyclic Aza-Andrographolide Derivatives from Late-Stage Hydroamination and Their Anti-human Coronavirus (Anti-HCoV) Activity.
Che, Chao; Jiang, Ding; Zhang, Jiayin; Xing, Qi; Li, Ting; Zhao, Yi; Guan, Liangyu; Chen, Huangcan; Xiang, Dehu; Di, Man; Zhu, Zhendong.
Afiliación
  • Che C; BayRay Innovative Center, Shenzhen Bay Laboratory, Shenzhen 518032, China.
  • Jiang D; State Key Laboratory of Chemical Oncogenomics, Guangdong Provincial Key Laboratory of Chemical Genomics, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
  • Zhang J; BayRay Innovative Center, Shenzhen Bay Laboratory, Shenzhen 518032, China.
  • Xing Q; BayRay Innovative Center, Shenzhen Bay Laboratory, Shenzhen 518032, China.
  • Li T; BayRay Innovative Center, Shenzhen Bay Laboratory, Shenzhen 518032, China.
  • Zhao Y; BayRay Innovative Center, Shenzhen Bay Laboratory, Shenzhen 518032, China.
  • Guan L; BayRay Innovative Center, Shenzhen Bay Laboratory, Shenzhen 518032, China.
  • Chen H; BayRay Innovative Center, Shenzhen Bay Laboratory, Shenzhen 518032, China.
  • Xiang D; BayRay Innovative Center, Shenzhen Bay Laboratory, Shenzhen 518032, China.
  • Di M; BayRay Innovative Center, Shenzhen Bay Laboratory, Shenzhen 518032, China.
  • Zhu Z; BayRay Innovative Center, Shenzhen Bay Laboratory, Shenzhen 518032, China.
ACS Omega ; 7(28): 24824-24837, 2022 Jul 19.
Article en En | MEDLINE | ID: mdl-35874238
ABSTRACT
A late-stage functionalization (LSF) of the natural product andrographolide for the efficient assembly of a range of structurally interesting and diverse tricyclic-aza derivatives was developed. The key to the diversification is a photo-catalyzed intramolecular hydroamination reaction, and acridinium derivatives were demonstrated to be the optimal catalysts. Additionally, the synthesized tricyclic aza-andrographolide derivatives were found to inhibit human coronavirus with high potency.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: ACS Omega Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: ACS Omega Año: 2022 Tipo del documento: Article País de afiliación: China