相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Stapled Peptides by Late-Stage C(sp3)-H Activation
Anais F. M. Noisier et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2017)
Adapting the Glaser Reaction for Bioconjugation: Robust Access to Structurally Simple, Rigid Linkers
Anthony P. Silvestri et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2017)
Design of Potent and Proteolytically Stable Oxyntomodulin Analogs
Avinash Muppidi et al.
ACS CHEMICAL BIOLOGY (2016)
Synthesis of Heterocycle-Bridged Peptidic Macrocycles through 1,3-Diyne Transformations
Steven Verlinden et al.
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (2016)
Development and Optimization of Glaser-Hay Bioconjugations
Jessica S. Lampkowski et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2015)
Acetone-Linked Peptides: A Convergent Approach for Peptide Macrocyclization and Labeling
Naila Assem et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2015)
Synthesis of antibacterial 1,3-diyne-linked peptoids from an Ugi-4CR/Glaser coupling approach
Martin C. N. Brauer et al.
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY (2015)
Peptide stapling techniques based on different macrocyclisation chemistries
Yu Heng Lau et al.
CHEMICAL SOCIETY REVIEWS (2015)
Oxidative α,ω-diyne coupling as an approach towards novel peptidic macrocycles
S. Verlinden et al.
ORGANIC & BIOMOLECULAR CHEMISTRY (2015)
A study on the protection of methionine and the reduction of methionine sulfoxide in methionine-containing analogues of the growth-modeling factor Gly-His-Lys
Monika Kukowska et al.
TETRAHEDRON LETTERS (2015)
Glaser oxidative coupling on peptides: Stabilization of β-turn structure via a 1,3-butadiyne constraint
Nicolas Auberger et al.
BIOORGANIC & MEDICINAL CHEMISTRY (2014)
Hydrocarbon-Stapled Peptides: Principles, Practice, and Progress
Loren D. Walensky et al.
JOURNAL OF MEDICINAL CHEMISTRY (2014)
HippDB: a database of readily targeted helical protein-protein interactions
Christina M. Bergey et al.
BIOINFORMATICS (2013)
A Perfluoroaryl-Cysteine SNAr Chemistry Approach to Unprotected Peptide Stapling
Alexander M. Spokoyny et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2013)
Design of Triazole-Stapled BCL9 α-Helical Peptides to Target the β-Catenin/B-Cell CLL/lymphoma 9 (BCL9) Protein-Protein Interaction
Steven A. Kawamoto et al.
JOURNAL OF MEDICINAL CHEMISTRY (2012)
Development of α-Helical Calpain Probes by Mimicking a Natural Protein-Protein Interaction
Hyunil Jo et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2012)
Reduced Sweetness of a Monellin (MNEI) Mutant Results from Increased Protein Flexibility and Disruption of a Distant Poly-(L-Proline) II Helix
Catherine M. Templeton et al.
CHEMICAL SENSES (2011)
Assessing Helical Protein Interfaces for Inhibitor Design
Brooke N. Bullock et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2011)
Contemporary strategies for peptide macrocyclization
ChHstcpher J. White et al.
NATURE CHEMISTRY (2011)
On Resin Side-Chain Cyclization of Complex Peptides Using CuAAC
Sampat Ingale et al.
ORGANIC LETTERS (2011)
Synthesis and conformational analysis of a cyclic peptide obtained via i to i+4 intramolecular side-chain to side-chain azide -: Alkyne 1,3-dipolar cycloaddition
Sonia Cantel et al.
JOURNAL OF ORGANIC CHEMISTRY (2008)
Crystal structure of a β-catenin/BCL9/Tcf4 complex
James Sampietro et al.
MOLECULAR CELL (2006)
The reduction of oxidized methionine residues in peptide thioesters with NH4I-Me2S
Christian P. R. Hackenberger
ORGANIC & BIOMOLECULAR CHEMISTRY (2006)
Synthesis of constrained helical peptides by thioether ligation: application to analogs of gp41
FM Brunel et al.
CHEMICAL COMMUNICATIONS (2005)
Activation of apoptosis in vivo by a hydrocarbon-stapled BH3 helix
LD Walensky et al.
SCIENCE (2004)
The growing impact of click chemistry on drug discovery
HC Kolb et al.
DRUG DISCOVERY TODAY (2003)
A versatile modification of on-column oligodeoxynucleotides using a copper-catalyzed oxidative acetylenic coupling reaction
N Minakawa et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2003)
An all-hydrocarbon cross-linking system for enhancing the helicity and metabolic stability of peptides
CE Schafmeister et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2000)