Sincalide corresponds to the C-terminal octapeptide of cholecystokinin (CCK) and acts on receptors within the gallbladder wall causing it to contract.
CAT No: 10-101-31
CAS No:25126-32-3 (net)
Synonyms/Alias:CCK-8; Cholecystokinin Octapeptide; (Des-Pyr1,Des-Gln2,Met5)-Caerulein
Sincalide Ammonium Salt is a synthetic peptide derivative that functions as an analog of the endogenous cholecystokinin octapeptide (CCK-8). As a member of the peptide hormone family, it is structurally designed to mimic the biological activities of natural cholecystokinin, which plays a pivotal role in gastrointestinal physiology. Its robust receptor-binding properties and well-characterized sequence make it an important research tool for investigating CCK-mediated signaling pathways. The compound's stability as an ammonium salt enhances its solubility and handling in laboratory settings, rendering it suitable for a variety of biochemical and pharmacological applications.
Receptor Pharmacology Studies: Sincalide analogs are extensively utilized in receptor binding assays to elucidate the affinity and specificity of cholecystokinin receptors, particularly CCK-A and CCK-B subtypes. By serving as a high-affinity ligand, the peptide enables researchers to map receptor distribution, study ligand-receptor interactions, and characterize downstream signaling mechanisms. These studies are fundamental for advancing the understanding of peptide hormone function and receptor pharmacodynamics in both normal and pathological states.
Gastrointestinal Motility Research: Due to its capacity to activate CCK receptors, this peptide is often employed in experimental models to investigate the regulation of smooth muscle contraction and gallbladder function. Its use in ex vivo organ bath studies and in vitro cell-based assays allows for precise quantification of contractile responses, providing valuable insights into the mechanisms governing gastrointestinal motility. Such research supports the development of novel strategies for modulating digestive processes and understanding peptide hormone regulation.
Signal Transduction Analysis: The ability of sincalide analogs to stimulate well-defined intracellular pathways makes them valuable probes for dissecting G protein-coupled receptor (GPCR) signaling cascades. In cellular models, the peptide can be used to trigger second messenger production, such as cyclic AMP or intracellular calcium flux, facilitating the study of downstream effectors and regulatory proteins. These mechanistic investigations are essential for delineating the molecular architecture of peptide-driven signal transduction.
Peptide Structure-Activity Relationship (SAR) Studies: The defined sequence and functional activity of this compound make it an ideal reference standard in SAR investigations. By comparing its biological effects to those of modified analogs, researchers can systematically evaluate the impact of specific amino acid substitutions on receptor affinity, efficacy, and selectivity. These studies are instrumental in guiding the rational design of novel peptide ligands with improved pharmacological profiles.
Analytical Method Development: Sincalide Ammonium Salt is frequently utilized as a calibration standard or positive control in analytical techniques such as high-performance liquid chromatography (HPLC) and mass spectrometry. Its well-characterized physicochemical properties enable accurate quantification and validation of analytical methods for peptide detection and purity assessment. This application is particularly valuable in quality control laboratories and research environments focused on peptide synthesis and characterization.
Collectively, the diverse applications of this peptide analog underscore its significance as a versatile research reagent in the fields of peptide pharmacology, gastrointestinal physiology, molecular signaling, and analytical chemistry. Its ability to reliably mimic endogenous cholecystokinin activity while offering enhanced stability and ease of use positions it as a preferred tool for advancing both fundamental and applied studies involving peptide hormones and their receptors.
To establish normal gallbladder ejection fraction (GBEF) values for two sincalide (cholecystokinin [CCK]) infusion dose rates, 0.01 microg per kilogram of body weight infused for 3 minutes and 0.01 microg/kg infused for 60 minutes.
Ziessman, H. A., Muenz, L. R., Agarwal, A. K., & ZaZa, A. A. (2001). Normal values for sincalide cholescintigraphy: comparison of two methods. Radiology, 221(2), 404-410.
2. An Open-label, Single-center, Safety and Efficacy Study of Eyelash Polygrowth Factor Serum
3. C-Peptide replacement therapy and sensory nerve function in type 1 diabetic neuropathy
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.