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Evaluation of a Cyclopentane-Based γ-Amino Acid for the Ability to Promote α/γ-Peptide Secondary Structure()

We report the asymmetric synthesis of the y-amino acid (1R,2R)-2-aminomethyl-1-cyclopentane carboxylic acid (AMCP) and an evaluation of this residue's potential to promote secondary structure in α/γ-peptides. Simulated annealing calculations using NMR-derived distance restraints obtained for α/...

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Autori principali: Giuliano, Michael W., Maynard, Stacy J., Almeida, Aaron M., Reidenbach, Andrew G., Guo, Li, Ulrich, Emily C., Guzei, Ilia A., Gellman, Samuel H.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2013
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4109159/
https://ncbi.nlm.nih.gov/pubmed/24303945
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo401501g
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