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Histidine-bridged cyclic peptide natural products: isolation, biosynthesis and synthetic studies.
Engelhardt, Pascal M; Keyzers, Robert; Brimble, Margaret A.
Afiliación
  • Engelhardt PM; School of Chemical Sciences, University of Auckland, 23 Symonds St., Auckland 1010, New Zealand. m.brimble@auckland.ac.nz.
  • Keyzers R; School of Chemical and Physical Sciences, Victoria University of Wellington, Laby Building Kelburn Parade, Wellington 6012, New Zealand. robert.keyzers@vuw.ac.nz.
  • Brimble MA; School of Chemical Sciences, University of Auckland, 23 Symonds St., Auckland 1010, New Zealand. m.brimble@auckland.ac.nz.
Org Biomol Chem ; 22(42): 8374-8396, 2024 10 30.
Article en En | MEDLINE | ID: mdl-39352687
ABSTRACT
The histidine bridge is a rare and often overlooked structural motif in macrocyclic peptide natural products, yet there are several examples in nature of cyclic peptides bearing this moiety that exhibit potent biological activity. These interesting compounds have been the focus of several studies reporting their isolation, biosynthesis and chemical synthesis over the last four decades. This review summarises the findings on the structure, biological activity and, where possible, proposed biosynthesis and progress towards the synthesis of histidine-bridged cyclic peptides.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Péptidos Cíclicos / Productos Biológicos / Histidina Límite: Humans Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Nueva Zelanda

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Péptidos Cíclicos / Productos Biológicos / Histidina Límite: Humans Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Nueva Zelanda