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Cyclic Aza-peptide Integrin Ligand Synthesis and Biological Activity | The Journal of Organic Chemistry
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Cyclic Aza-peptide Integrin Ligand Synthesis and Biological Activity | The Journal of Organic Chemistry
Exploring Side-Chain Diversity by Submonomer Solid-Phase Aza-Peptide Synthesis | Organic Letters
PDF) Productivity Improving of Artichoke in Organic Farming by Compost and Compost Tea Fertilization
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Cyclic Aza-peptide Integrin Ligand Synthesis and Biological Activity | The Journal of Organic Chemistry
Dynamic Chirality in the Mechanism of Action of Allosteric CD36 Modulators of Macrophage-Driven Inflammation | Journal of Medicinal Chemistry
PDF) Effects of Organic Amendments to Soil on Pepper crop (Capsicum Annuum, L.) under green house
Scheme 7. Synthesis of aza-pipecolate-GHRP-6 analogues 78-82.... | Download Scientific Diagram
Future Pharmacology | Free Full-Text | Azapeptides as an Efficient Tool to Improve the Activity of Biologically Effective Peptides
top) Sequence representation of CMPs 6c, 14c, and 20c. (a) Graphical... | Download Scientific Diagram
Solid-Phase Azopeptide Diels–Alder Chemistry for Aza-pipecolyl Residue Synthesis To Study Peptide Conformation | The Journal of Organic Chemistry
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Future Pharmacology | Free Full-Text | Azapeptides as an Efficient Tool to Improve the Activity of Biologically Effective Peptides
Aza-Amino Acid Scan for Rapid Identification of Secondary Structure Based on the Application of N-Boc-Aza1-Dipeptides in Peptide Synthesis | Journal of the American Chemical Society
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Solid-Phase Azopeptide Diels–Alder Chemistry for Aza-pipecolyl Residue Synthesis To Study Peptide Conformation | The Journal of Organic Chemistry
Future Pharmacology | Free Full-Text | Azapeptides as an Efficient Tool to Improve the Activity of Biologically Effective Peptides
Aza-Amino Acid Scanning of Secondary Structure Suited for Solid-Phase Peptide Synthesis with Fmoc Chemistry and Aza-Amino Acids with Heteroatomic Side Chains | ACS Combinatorial Science
Structural Optimization of Azadipeptide Nitriles Strongly Increases Association Rates and Allows the Development of Selective Cathepsin Inhibitors | Journal of Medicinal Chemistry
