Zobrazeno 1 - 6
of 6
pro vyhledávání: '"unnatural γ-amino acids"'
Autor:
Francesco Oliva, Raffaella Bucci, Lucia Tamborini, Stefano Pieraccini, Andrea Pinto, Sara Pellegrino
Publikováno v:
Frontiers in Chemistry, Vol 7 (2019)
Unnatural amino acids have tremendously expanded the folding possibilities of peptides and peptide mimics. While α,α-disubstituted and β-amino acids are widely studied, γ-derivatives have been less exploited. Here we report the conformational stu
Externí odkaz:
https://doaj.org/article/73d2bfa42264473cb4994aa649c83d9d
Autor:
Ona Illa, José-Antonio Olivares, Nerea Gaztelumendi, Laura Martínez-Castro, Jimena Ospina, María-Ángeles Abengozar, Giuseppe Sciortino, Jean-Didier Maréchal, Carme Nogués, Míriam Royo, Luis Rivas, Rosa M. Ortuño
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 20, p 7502 (2020)
Two series of new hybrid γ/γ-peptides, γ-CC and γ-CT, formed by (1S,2R)-3-amino-2,2,dimethylcyclobutane-1-carboxylic acid joined in alternation to a Nα-functionalized cis- or trans-γ-amino-l-proline derivative, respectively, have been synthesiz
Externí odkaz:
https://doaj.org/article/976a732b116b4ee8b16dc87fd4099408
Autor:
Carme Nogués, María-Ángeles Abengozar, Ona Illa, Luis Rivas, Jean-Didier Maréchal, Giuseppe Sciortino, Nerea Gaztelumendi, José Antonio Olivares, Laura Martínez-Castro, Miriam Royo, Rosa M. Ortuño, Jimena Ospina
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
International Journal of Molecular Sciences, Vol 21, Iss 7502, p 7502 (2020)
International Journal of Molecular Sciences
Volume 21
Issue 20
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
International Journal of Molecular Sciences, Vol 21, Iss 7502, p 7502 (2020)
International Journal of Molecular Sciences
Volume 21
Issue 20
Two series of new hybrid &gamma
/&gamma
peptides, &gamma
CC and &gamma
CT, formed by (1S,2R)-3-amino-2,2,dimethylcyclobutane-1-carboxylic acid joined in alternation to a N&alpha
functionalized cis- or trans-&gamma
amino-
/&gamma
peptides, &gamma
CC and &gamma
CT, formed by (1S,2R)-3-amino-2,2,dimethylcyclobutane-1-carboxylic acid joined in alternation to a N&alpha
functionalized cis- or trans-&gamma
amino-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea51ef536f10530f98f4779cf926f0a6
https://ddd.uab.cat/record/233888
https://ddd.uab.cat/record/233888
Autor:
Lucia Tamborini, Francesco Oliva, Raffaella Bucci, Sara Pellegrino, Stefano Pieraccini, Andrea Pinto
Publikováno v:
Frontiers in Chemistry
Frontiers in Chemistry, Vol 7 (2019)
Frontiers in Chemistry, Vol 7 (2019)
Unnatural amino acids have tremendously expanded the folding possibilities of peptides and peptide mimics. While α,α-disubstituted and β-amino acids are widely studied, γ-derivatives have been less exploited. Here we report the conformational stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c26c538fb91e7d63677a8d6871ac15b3
https://pubmed.ncbi.nlm.nih.gov/30937302
https://pubmed.ncbi.nlm.nih.gov/30937302
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Akademický článek
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