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Synthesis of a hexahydropyrrolo indole (HPI) compound library.
Nickel, Sabrina; Nickel, Philipp; Hellmert, Marco; Ernst, Silvia; Jewell, Robert; Pearce, Christopher A; Jones, Geraint; Hamza, Daniel; Kaiser, Markus.
Afiliação
  • Nickel S; Chemical Biology, Zentrum für Medizinische Biotechnologie (ZMB), Fakultät für Biologie, Universtität Duisburg-Essen, Universitätsstr. 2, 45117 Essen, Germany.
  • Nickel P; Chemical Biology, Zentrum für Medizinische Biotechnologie (ZMB), Fakultät für Biologie, Universtität Duisburg-Essen, Universitätsstr. 2, 45117 Essen, Germany.
  • Hellmert M; Chemical Biology, Zentrum für Medizinische Biotechnologie (ZMB), Fakultät für Biologie, Universtität Duisburg-Essen, Universitätsstr. 2, 45117 Essen, Germany.
  • Ernst S; Chemical Biology, Zentrum für Medizinische Biotechnologie (ZMB), Fakultät für Biologie, Universtität Duisburg-Essen, Universitätsstr. 2, 45117 Essen, Germany.
  • Jewell R; Sygnature Discovery, BioCity, Pennyfoot Street, Nottingham NG1 1GF, United Kingdom.
  • Pearce CA; Sygnature Discovery, BioCity, Pennyfoot Street, Nottingham NG1 1GF, United Kingdom.
  • Jones G; Sygnature Discovery, BioCity, Pennyfoot Street, Nottingham NG1 1GF, United Kingdom.
  • Hamza D; Sygnature Discovery, BioCity, Pennyfoot Street, Nottingham NG1 1GF, United Kingdom.
  • Kaiser M; Chemical Biology, Zentrum für Medizinische Biotechnologie (ZMB), Fakultät für Biologie, Universtität Duisburg-Essen, Universitätsstr. 2, 45117 Essen, Germany. Electronic address: markus.kaiser@uni-due.de.
Bioorg Med Chem ; 23(11): 2636-45, 2015 Jun 01.
Article em En | MEDLINE | ID: mdl-25907365
ABSTRACT
Scaffolds of natural products represent promising starting points for the development of focused compound libraries. Here, we describe the development of a synthetic route to a compound library based on the hexahydropyrrolo indole (HPI) scaffold, the denoting structural motif of the HPI natural product family. To this end, a two-step approach consisting of a batch synthesis of an advanced functionalizable HPI intermediate followed by the establishment of reaction conditions that allow derivatization of this scaffold at three different positions is described. Subsequently, the optimized methods were applied to the synthesis of a 276-member library.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Produtos Biológicos / Bibliotecas de Moléculas Pequenas / Descoberta de Drogas / Indóis Idioma: En Revista: Bioorg Med Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Produtos Biológicos / Bibliotecas de Moléculas Pequenas / Descoberta de Drogas / Indóis Idioma: En Revista: Bioorg Med Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Alemanha