Atosiban (free acid) Trifluoroacetate features a modified peptide sequence containing both cyclic and linear elements. Researchers examine its receptor-binding determinants and conformational adaptability. Charge and hydrophobic balance influence solubility and folding. Applications include structural mapping, ligand-binding studies, and sequence-engineering research.
CAT No: R2560
CAS No:168102-69-0
Synonyms/Alias:168102-69-0;Atosiban (free acid) Trifluoroacetate;2-[[(2S)-5-amino-2-[[(2S)-1-[(4R,7S,10S,16R)-7-(2-amino-2-oxoethyl)-13-[(2S)-butan-2-yl]-16-[(4-ethoxyphenyl)methyl]-10-[(1R)-1-hydroxyethyl]-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentazacycloicosane-4-carbonyl]pyrrolidine-2-carbonyl]amino]pentanoyl]amino]acetic acid;2,2,2-trifluoroacetic acid;DA-59745;
Atosiban (free acid) Trifluoroacetate is a synthetic peptide compound designed to function as an oxytocin and vasopressin receptor antagonist. Structurally, it is a cyclic nonapeptide, and the inclusion of the trifluoroacetate counterion facilitates its formulation and handling in research environments. The compound's primary biochemical relevance lies in its high specificity for the oxytocin receptor, as well as its ability to modulate vasopressin-mediated pathways. This dual antagonistic profile has made it a valuable molecular tool in the investigation of peptide hormone signaling, receptor pharmacology, and the physiological roles of oxytocin and vasopressin in various biological systems.
Receptor binding assays: Atosiban is frequently employed in receptor binding studies to quantitatively assess the affinity and selectivity of ligands for oxytocin and vasopressin receptors. By functioning as a competitive antagonist, it enables researchers to delineate the binding characteristics of these receptors in tissue preparations, cell-based assays, or membrane fractions. Such applications are fundamental for characterizing receptor-ligand interactions, mapping binding sites, and supporting the development of novel receptor modulators.
Signal transduction research: The compound is widely used to dissect downstream signaling pathways activated by oxytocin and vasopressin receptors. By inhibiting receptor activation, it allows for controlled studies of G protein-coupled receptor (GPCR) signaling cascades, including second messenger production, calcium mobilization, and kinase activation. This approach is essential for elucidating the molecular mechanisms underlying peptide hormone action and for distinguishing receptor-specific effects in complex biological systems.
Functional studies in smooth muscle physiology: Atosiban serves as a critical tool in functional assays examining the contractile responses of smooth muscle tissues, particularly in the uterus and vascular system. Researchers utilize its antagonistic properties to investigate the contribution of oxytocin and vasopressin signaling to muscle tone regulation, contraction dynamics, and tissue responsiveness under various experimental conditions. These studies provide mechanistic insights into the physiological roles of peptide hormones in reproductive and vascular biology.
Pharmacological profiling: The compound is integral to the pharmacological characterization of novel compounds targeting the oxytocin and vasopressin receptor families. It is commonly used as a reference antagonist in competitive binding and functional activity assays, enabling the comparison of new ligands' potency, efficacy, and selectivity. Such profiling supports drug discovery efforts and advances the understanding of receptor subtype pharmacology.
Peptide synthesis and analytical method development: Atosiban (free acid) Trifluoroacetate is also utilized as a reference material in peptide synthesis optimization and in the development of analytical methods for peptide quantification and characterization. Its defined structure and receptor specificity make it a suitable standard for validating chromatographic, spectrometric, or immunoassay techniques, thereby ensuring accuracy and reliability in peptide research workflows.
1. An Open-label, Single-center, Safety and Efficacy Study of Eyelash Polygrowth Factor Serum
4. Adipose tissue is a key organ for the beneficial effects of GLP-2 metabolic function
5. Cell-based adhesion assays for isolation of snake venom’s integrin antagonists
If you have any peptide synthesis requirement in mind, please do not hesitate to contact us at . We will endeavor to provide highly satisfying products and services.
Creative Peptides is a trusted CDMO partner specializing in high-quality peptide synthesis, conjugation, and manufacturing under strict cGMP compliance. With advanced technology platforms and a team of experienced scientists, we deliver tailored peptide solutions to support drug discovery, clinical development, and cosmetic innovation worldwide.
From custom peptide synthesis to complex peptide-drug conjugates, we provide flexible, end-to-end services designed to accelerate timelines and ensure regulatory excellence. Our commitment to quality, reliability, and innovation has made us a preferred partner across the pharmaceutical, biotechnology, and personal care industries.