New strategies for the design of folded peptoids revealed by a survey of noncovalent interactions in model systems - Wikidata - awgldk - TriplyDB

New strategies for the design of folded peptoids revealed by a survey of noncovalent interactions in model systems

New strategies for the design of folded peptoids revealed by a survey of noncovalent interactions in model systems

http://www.wikidata.org/entity/Q33512972

about

n-->pi* interactions in proteins Systematic conformational investigations of peptoids and peptoid-peptide chimeras.Interplay of hydrogen bonds and n→π* interactions in proteins Triangular prism-shaped β-peptoid helices as unique biomimetic scaffolds Towards vast libraries of scaffold-diverse, conformationally constrained oligomers.Development of homomultimers and heteromultimers of lung cancer-specific peptoids.Synthesis of libraries of peptidomimetic compounds containing a 2-oxopiperazine unit in the main chain.13C NMR spectroscopy for the quantitative determination of compound ratios and polymer end groups.Split-and-pool synthesis and characterization of peptide tertiary amide library Sequence Programmable Peptoid Polymers for Diverse Materials Applications.A peptoid ribbon secondary structure.Beta-peptoid "foldamers"--why the additional methylene unit?Antimicrobial β-peptides and α-peptoids.Peptides and proteins as a continuing exciting source of inspiration for peptidomimetics.Microwave heating in solid-phase peptide synthesis.Progress in the de novo design of structured peptoid protein mimics.Peptide and peptoid foldamers in medicinal chemistry.Handedness preference and switching of peptide helices. Part II: Helices based on noncoded α-amino acids.The n → π* interaction: a rapidly emerging non-covalent interaction.Construction of peptoids with all trans-amide backbones and peptoid reverse turns via the tactical incorporation of N-aryl side chains capable of hydrogen bonding An overview of peptide and peptoid foldamers in medicinal chemistry.Extraordinarily robust polyproline type I peptoid helices generated via the incorporation of α-chiral aromatic N-1-naphthylethyl side chains.Reciprocal carbonyl-carbonyl interactions in small molecules and proteins.The n→π* Interaction Intimate interactions with carbonyl groups: dipole-dipole or n→π*?n→π* interactions engender chirality in carbonyl groups Signature of n→π* interactions in α-helices.Rapid photoassisted access to N,O,S-polyheterocycles with benzoazocine and hydroquinoline cores: intramolecular cycloadditions of photogenerated azaxylylenes A conserved interaction with the chromophore of fluorescent proteins.A key n→π* Interaction in N-acyl homoserine lactones.Design and conformational analysis of peptoids containing N-hydroxy amides reveals a unique sheet-like secondary structure.n→π* interactions of amides and thioamides: implications for protein stability.Ester vs. amide on folding: a case study with a 2-residue synthetic peptide.Peptide Solubility Limits: Backbone and Side-Chain Interactions.β-Peptoids: synthesis of a novel dimer having a fully extended conformation.A Pure Polyproline Type I-like Peptoid Helix by Metal Coordination.Use of the environmentally sensitive fluorophore 4-N,N-dimethylamino-1,8-naphthalimide to study peptoid helix structures.Peptoids at the 7th Summit: Toward macromolecular systems engineering Conformational selectivity and high-affinity binding in the complexation of -phenyl amides in water by a phenyl extended calix[4]pyrrole Expedient Solution-Phase Synthesis and NMR Studies of Arylopeptoids

P2860

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P2860

New strategies for the design of folded peptoids revealed by a survey of noncovalent interactions in model systems

http://www.wikidata.org/entity/Q33512972

description

2009 nî lūn-bûn

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2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2009 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

New strategies for the design ...... interactions in model systems

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New strategies for the design ...... interactions in model systems

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New strategies for the design ...... interactions in model systems

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New strategies for the design ...... interactions in model systems

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New strategies for the design ...... interactions in model systems

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New strategies for the design ...... interactions in model systems.

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Journal of the American Chemical Society

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New strategies for the design ...... interactions in model systems

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P2093

Benjamin C Gorske

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Brent L Bastian

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Helen E Blackwell

http://www.w3.org/2001/XMLSchema#string

Joseph R Stringer

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Sarah A Fowler

http://www.w3.org/2001/XMLSchema#string

P2860

Improving SH3 domain ligand selectivity using a non-natural scaffold.

An electronic effect on protein structure.

Energetics of an n --> pi interaction that impacts protein structure.

(19)F-encoded combinatorial libraries: discovery of selective metal binding and catalytic peptoids.

Molecular diversity through sugar scaffolds.

Identification from a positional scanning peptoid library of in vivo active compounds that neutralize bacterial endotoxins.

Peptoids: a modular approach to drug discovery.

Protein "fingerprinting" in complex mixtures with peptoid microarrays.

The Trp cage motif as a scaffold for the display of a randomized peptide library on bacteriophage T7.

Strategies for the use of mixture-based synthetic combinatorial libraries: scaffold ranking, direct testing in vivo, and enhanced deconvolution by computational methods.

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16555-16567

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10.1021/JA907184G

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45

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131

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2009-11-01T00:00:00Z

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38039677

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19860427

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3175426

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