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Stapled peptide
Stapled Α−Helical Peptide Drug Development: a Potent PNAS PLUS Dual Inhibitor of MDM2 and MDMX for P53-Dependent Cancer Therapy
A Short Double-Stapled Peptide Inhibits Respiratory Syncytial Virus Entry and Spreading
Stapled Peptides—A Useful Improvement for Peptide-Based Drugs
Nonproteinogenic Deep Mutational Scanning of Linear and Cyclic Peptides
Peptide Technologies at Energypolis
Functionalised Staple Linkages for Modulating The
Rapid Optimization of Mcl-1 Inhibitors Using Stapled Peptide Libraries Including Non-Natural Side Chains
Investigation of Nitrile Oxide-Alkyne 1,3-Dipolar Cycloadditions and Their Potential Viability for Synthesis of Stapled Peptides
1 Design and Development of Stapled Transmembrane Peptides That
Peptide Stapling Techniques Based on Different Macrocyclisation Chemistries
Stapled Peptide Targeting the CDK4/Cyclin D Interface Combined
Unprotected Peptide Macrocyclization and Stapling Via a Fluorine-Thiol
Discovery and Optimization of Peptide Macrocycles
Hydrocarbon Double-Stapling Remedies the Proteolytic Instability of a Lengthy Peptide Therapeutic
Macrocyclization of an All-D Linear Peptide Improves Target Affinity and Imparts Cellular Activity: a Novel Stapled −Helical Peptide Modality
Stapled Peptides Inhibitors: a New Window for Target Drug Discovery
Development and Evaluation of Novel Hydrocarbon Stapled Peptidomimetics with Future Application to Bionic Proteins
Hitting “Undruggable” Targets: Determining the Properties of Cell Penetrant Stabilized Peptide Therapeutics for Intracellular Targets
Top View
Interface Peptide Mimetics-Rationale and Application As Therapeutic Agents
Regulation of Protein–Protein Interactions Using Stapled Peptides
Stapled Peptide Design: Principles and Roles of Computation
A Comprehensive Review on Current Advances in Peptide Drug Development and Design
Peptide and Nonpeptide Approaches to Target Protein- Protein Interactions for the Treatment of Cancer