Acetone-Linked Peptides: A Convergent Approach for Peptide Macrocyclization and Labeling. - Test2 - elhamkhani - TriplyDB

Acetone-Linked Peptides: A Convergent Approach for Peptide Macrocyclization and Labeling.

Acetone-Linked Peptides: A Convergent Approach for Peptide Macrocyclization and Labeling.

http://www.wikidata.org/entity/Q36775960

about

Constraining an Irregular Peptide Secondary Structure through Ring-Closing Alkyne Metathesis Phage-displayed macrocyclic glycopeptide libraries.Click-Based Libraries of SFTI-1 Peptides: New Methods Using Reversed-Phase Silica.Linker-free incorporation of carbohydrates into in vitro displayed macrocyclic peptides.Converting disulfide bridges in native peptides to stable methylene thioacetals.Selective chemical labeling of proteins.Oxime conjugation in protein chemistry: from carbonyl incorporation to nucleophilic catalysis.Designing helical peptide inhibitors of protein-protein interactions Review stapling peptides using cysteine crosslinking.Thioether-Derived Macrocycle for Peptide Secondary Structure Fixation.Orthogonal ring-closing alkyne and olefin metathesis for the synthesis of small GTPase-targeting bicyclic peptides.Next-generation disulfide stapling: reduction and functional re-bridging all in one.Peptide Macrocyclization Inspired by Non-Ribosomal Imine Natural Products.Double quick, double click reversible peptide "stapling".Nitrogen Arylation for Macrocyclization of Unprotected Peptides.Oxetane Grafts Installed Site-Selectively on Native Disulfides to Enhance Protein Stability and Activity In Vivo.De novo design of covalently constrained mesosize protein scaffolds with unique tertiary structures.Adapting the Glaser Reaction for Bioconjugation: Robust Access to Structurally Simple, Rigid Linkers.Locking Interconversion of Aromatic Oligoamide Foldamers by Intramolecular Side-chain Crosslinking: toward Absolute Control of Helicity in Synthetic Aromatic Foldamers.Stabilization of peptides against proteolysis through disulfide-bridged conjugation with synthetic aromatics.Diversity-Oriented Peptide Stapling: A Third Generation Copper-Catalysed Azide-Alkyne Cycloaddition Stapling and Functionalisation Strategy.Diversity-Oriented Synthesis of Cyclic Azapeptides by A3 -Macrocyclization Provides High-Affinity CD36-Modulating Peptidomimetics.Enhanced Permeability and Binding Activity of Isobutylene-Grafted Peptides.A precisely positioned chiral center in an i, i + 7 tether modulates the helicity of the backbone peptide.Precisely Regulated and Efficient Locking of Linear Peptides into Stable Multicyclic Topologies through a One-Pot Reaction.Stapling of unprotected helical peptides via photo-induced intramolecular thiol-yne hydrothiolation.

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P2860

Acetone-Linked Peptides: A Convergent Approach for Peptide Macrocyclization and Labeling.

http://www.wikidata.org/entity/Q36775960

description

2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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2015年论文

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2015年论文

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name

Acetone-Linked Peptides: A Convergent Approach for Peptide Macrocyclization and Labeling.

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Acetone-Linked Peptides: A Convergent Approach for Peptide Macrocyclization and Labeling.

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Acetone-Linked Peptides: A Convergent Approach for Peptide Macrocyclization and Labeling.

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Acetone-Linked Peptides: A Convergent Approach for Peptide Macrocyclization and Labeling.

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Acetone-Linked Peptides: A Convergent Approach for Peptide Macrocyclization and Labeling.

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Acetone-Linked Peptides: A Convergent Approach for Peptide Macrocyclization and Labeling.

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Angewandte Chemie International Edition

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Acetone-Linked Peptides: A Convergent Approach for Peptide Macrocyclization and Labeling.

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David J Ferreira

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Naila Assem

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Philip E Dawson

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P2860

A stapled BID BH3 helix directly binds and activates BAX

All-atom model for stabilization of alpha-helical structure in peptides by hydrocarbon staples.

Structural and thermodynamic consequences of introducing alpha-aminoisobutyric acid in the S peptide of ribonuclease S

Refinement of the crystal structure of ribonuclease S. Comparison with and between the various ribonuclease A structures

Stapled α−helical peptide drug development: A potent dual inhibitor of MDM2 and MDMX for p53-dependent cancer therapy

Discovery of a Potent Stapled Helix Peptide That Binds to the 70N Domain of Replication Protein A

Alpha-helix nucleation by a calcium-binding peptide loop

The preparation of subtilisn-modified ribonuclease and the separation of the peptide and protein components

A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes

Nucleophilic catalysis of oxime ligation

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scholarly article

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10.1002/ANIE.201502607

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30

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54

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Dennis W. Wolan

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2015-06-11T00:00:00Z

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26096515

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