(D-Leu2)-Melanocyte-Stimulating Hormone-Release Inhibiting Factor incorporates a stereochemical substitution that modulates conformation and receptor interaction. The peptide supports investigations into neuropeptide signaling and regulatory cross-talk in endocrine pathways. Its modified residue influences resistance to enzymatic cleavage in vitro. Researchers employ it in receptor binding, structural modeling, and peptidomimetic design.
3. Emerging applications of nanotechnology for diagnosis and therapy of disease: a review
4. Implications of ligand-receptor binding kinetics on GLP-1R signalling
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