Exploring the conformational and biological versatility of β-turn-modified gramicidin S by using sugar amino acid homologues that vary in ring size.
about
Hairpin formation promoted by the heterochiral dinipecotic acid segment: A DFT study.A compendium of cyclic sugar amino acids and their carbocyclic and heterocyclic nitrogen analogues.Structure, toxicity and antibiotic activity of gramicidin S and derivativesSquare sugars: challenges and synthetic strategies.Computationally designed β-turn foldamers of γ-peptides based on 2-(aminomethyl)cyclohexanecarboxylic acid
P2860
Exploring the conformational and biological versatility of β-turn-modified gramicidin S by using sugar amino acid homologues that vary in ring size.
description
2011 nî lūn-bûn
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2011年の論文
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2011年学术文章
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name
Exploring the conformational a ...... logues that vary in ring size.
@en
Exploring the conformational a ...... logues that vary in ring size.
@nl
type
label
Exploring the conformational a ...... logues that vary in ring size.
@en
Exploring the conformational a ...... logues that vary in ring size.
@nl
prefLabel
Exploring the conformational a ...... logues that vary in ring size.
@en
Exploring the conformational a ...... logues that vary in ring size.
@nl
P2093
P2860
P50
P356
P1476
Exploring the conformational a ...... logues that vary in ring size.
@en
P2093
Adriaan W Tuin
Albert J de Neeling
Annemiek D Knijnenburg
Daan Noort
Emile Spalburg
Gijs A van der Marel
José M Otero
Mark Overhand
Roos H Mars-Groenendijk
P2860
P304
P356
10.1002/CHEM.201002895
P407
P577
2011-03-01T00:00:00Z