N(1)Gly-DL-Phe-DL-xiIle-Gly-DL-Trp-Gly-DL-Asn-DL-Asp(1)-DL-xiIle-DL-Phe-Gly-DL-Ala(imidazol-2-yl)(imidazol-2-yl)-DL-Tyr-DL-Ser-Gly-DL-Asp-DL-Phe-OH presents a complex multi-residue architecture containing D/L stereochemistry and heterocyclic modifications. The abundant diversity of hydrophobic, aromatic, and acidic residues shapes a dynamic conformational landscape. Researchers use it to explore folding pathways, charge distribution, and binding equilibria. Applications extend to peptide engineering, structural analysis, and sequence-function correlation studies.
CAT No: R2457
CAS No:133658-45-4
Synonyms/Alias:N(1)Gly-DL-Phe-DL-xiIle-Gly-DL-Trp-Gly-DL-Asn-DL-Asp(1)-DL-xiIle-DL-Phe-Gly-DL-Ala(imidazol-2-yl)(imidazol-2-yl)-DL-Tyr-DL-Ser-Gly-DL-Asp-DL-Phe-OH;133658-45-4;N(1)Gly-DL-Phe-DL-xiIle-Gly-DL-Trp-Gly-DL-Asn-DL-Asp(1)-DL-xiIle-DL-Phe-Gly-DL-Ala(imidazol-2-yl)-DL-Tyr-DL-Ser-Gly-DL-Asp-DL-Phe-OH;
1. High fat diet and GLP-1 drugs induce pancreatic injury in mice
2. Myotropic activity of allatostatins in tenebrionid beetles
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