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Solid-Phase Synthesis of N-Substituted Glycine Oligomers (α-Peptoids) and Derivatives

Peptoids (N-substituted polyglycines and extended peptoids with variant backbone amino-acid monomer units) are oligomeric synthetic polymers that are becoming a valuable molecular tool in the biosciences. Of particular interest are their applications to the exploration of peptoid secondary structure...

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Detalles Bibliográficos
Autores principales: Culf, Adrian S., Ouellette, Rodney J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257730/
https://www.ncbi.nlm.nih.gov/pubmed/20714299
http://dx.doi.org/10.3390/molecules15085282
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author Culf, Adrian S.
Ouellette, Rodney J.
author_facet Culf, Adrian S.
Ouellette, Rodney J.
author_sort Culf, Adrian S.
collection PubMed
description Peptoids (N-substituted polyglycines and extended peptoids with variant backbone amino-acid monomer units) are oligomeric synthetic polymers that are becoming a valuable molecular tool in the biosciences. Of particular interest are their applications to the exploration of peptoid secondary structures and drug design. Major advantages of peptoids as research and pharmaceutical tools include the ease and economy of synthesis, highly variable backbone and side-chain chemistry possibilities. At the same time, peptoids have been demonstrated as highly active in biological systems while resistant to proteolytic decay. This review with 227 references considers the solid-phase synthetic aspects of peptoid preparation and utilization up to 2010 from the instigation, by R. N. Zuckermann et al., of peptoid chemistry in 1992.
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spelling pubmed-62577302018-12-06 Solid-Phase Synthesis of N-Substituted Glycine Oligomers (α-Peptoids) and Derivatives Culf, Adrian S. Ouellette, Rodney J. Molecules Review Peptoids (N-substituted polyglycines and extended peptoids with variant backbone amino-acid monomer units) are oligomeric synthetic polymers that are becoming a valuable molecular tool in the biosciences. Of particular interest are their applications to the exploration of peptoid secondary structures and drug design. Major advantages of peptoids as research and pharmaceutical tools include the ease and economy of synthesis, highly variable backbone and side-chain chemistry possibilities. At the same time, peptoids have been demonstrated as highly active in biological systems while resistant to proteolytic decay. This review with 227 references considers the solid-phase synthetic aspects of peptoid preparation and utilization up to 2010 from the instigation, by R. N. Zuckermann et al., of peptoid chemistry in 1992. MDPI 2010-08-04 /pmc/articles/PMC6257730/ /pubmed/20714299 http://dx.doi.org/10.3390/molecules15085282 Text en © 2010 by the authors; licensee MDPI, Basel, Switzerland. This article is an Open Access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Culf, Adrian S.
Ouellette, Rodney J.
Solid-Phase Synthesis of N-Substituted Glycine Oligomers (α-Peptoids) and Derivatives
title Solid-Phase Synthesis of N-Substituted Glycine Oligomers (α-Peptoids) and Derivatives
title_full Solid-Phase Synthesis of N-Substituted Glycine Oligomers (α-Peptoids) and Derivatives
title_fullStr Solid-Phase Synthesis of N-Substituted Glycine Oligomers (α-Peptoids) and Derivatives
title_full_unstemmed Solid-Phase Synthesis of N-Substituted Glycine Oligomers (α-Peptoids) and Derivatives
title_short Solid-Phase Synthesis of N-Substituted Glycine Oligomers (α-Peptoids) and Derivatives
title_sort solid-phase synthesis of n-substituted glycine oligomers (α-peptoids) and derivatives
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257730/
https://www.ncbi.nlm.nih.gov/pubmed/20714299
http://dx.doi.org/10.3390/molecules15085282
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