Kisspeptin-10, rat contains aromatic, basic, and hydrophobic residues arranged to promote defined receptor-binding surfaces. The peptide supports investigations of helix formation, residue-residue coupling, and solvent-driven structural transitions. Researchers use it to map ligand-recognition motifs and examine conformational energetics. Its compact length enables high-resolution analysis.
CAT No: R2281
CAS No:478507-53-8
Synonyms/Alias:Kisspeptin-10, rat;478507-53-8;CHEMBL3422406;L-Tyrosinamide,L-tyrosyl-L-asparaginyl-L-tryptophyl-L-asparaginyl-L-seryl-L-phenylalanylglycyl-L-leucyl-L-arginyl-;Kisspeptin-10 (mouse, rat);SCHEMBL17345398;HY-P1197;BDBM50082075;AKOS024458053;DA-54639;CS-0028953;(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-amino-3-(4-hydroxyphenyl)propanamido]-3-carbamoylpropanamido]-3-(1H-indol-3-yl)propanamido]-N-[(1S)-1-{[(1S)-1-[({[(1S)-1-{[(1S)-4-carbamimidamido-1-{[(1S)-1-carbamoyl-2-(4-hydroxyphenyl)ethyl]carbamoyl}butyl]carbamoyl}-3-methylbutyl]carbamoyl}methyl)carbamoyl]-2-phenylethyl]carbamoyl}-2-hydroxyethyl]succinamide;
1. The spatiotemporal control of signalling and trafficking of the GLP-1R
2. Emerging applications of nanotechnology for diagnosis and therapy of disease: a review
4. TMEM16F and dynamins control expansive plasma membrane reservoirs
5. Immune responses to homocitrulline-and citrulline-containing peptides in rheumatoid arthritis
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