(Phe1-psi(CH₂NH)Gly2)-Nociceptin (1-13) amide contains a reduced amide bond surrogate that alters backbone geometry and enzymatic susceptibility. The fragment preserves key hydrophobic residues needed for ligand recognition. Its amidated terminus enhances conformational stability. Research uses include analog comparison, structural analysis, and receptor-interface investigations.
2. Store-operated Ca2+ entry sustains the fertilization Ca2+ signal in pig eggs
3. Emu oil in combination with other active ingredients for treating skin imperfections
5. Adipose tissue is a key organ for the beneficial effects of GLP-2 metabolic function
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