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Current Understanding toward Isonitrile Group Biosynthesis and Mechanism.
Chen, Tzu-Yu; Chen, Jinfeng; Tang, Yijie; Zhou, Jiahai; Guo, Yisong; Chang, Wei-Chen.
Afiliação
  • Chen TY; Department of Chemistry, North Carolina State University Raleigh, NC 27695, U.S.A.
  • Chen J; State Key Laboratory of Bio-organic and Natural Products Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Shanghai 200032, China.
  • Tang Y; Department of Chemistry, Carnegie Mellon University, Pittsburgh, PA 15213, U.S.A.
  • Zhou J; State Key Laboratory of Bio-organic and Natural Products Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Shanghai 200032, China.
  • Guo Y; CAS Key Laboratory of Quantitative Engineering Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, Guangdong 518055, China.
  • Chang WC; Department of Chemistry, Carnegie Mellon University, Pittsburgh, PA 15213, U.S.A.
Chin J Chem ; 39(2): 463-472, 2021 Feb.
Article em En | MEDLINE | ID: mdl-34658601
ABSTRACT
Isonitrile group has been identified in many natural products. Due to the broad reactivity of N≡C triple bond, these natural products have valuable pharmaceutical potentials. This review summarizes the current biosynthetic pathways and the corresponding enzymes that are responsible for isonitrile-containing natural product generation. Based on the strategies utilized, two fundamentally distinctive approaches are discussed. In addition, recent progress in elucidating isonitrile group formation mechanisms is also presented.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article