CID 162678814 is a database-registered peptide-like molecule used for modeling structural determinants of ligand binding. Hydrophobic and polar functionalities provide adaptable conformational states. Researchers investigate its affinity patterns and hydrogen-bond networks. Applications span screening campaigns, scaffold optimization, and molecular-recognition studies.
CAT No: PI-025
CAS No:1872435-09-0
Synonyms/Alias:1872435-09-0;HY-P2519;AKOS040755165;DA-57152;PD133800;CS-0135063;(2S)-1-[(2S)-2-[[2-[[(2S)-2-[[(2S)-2-[[(2S,3R)-2-amino-3-hydroxybutanoyl]amino]-3-phenylpropanoyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]acetyl]amino]propanoyl]pyrrolidine-2-carboxamide;
CID 162678814 is a unique carbohydrate compound recognized for its specialized structure and versatile chemical properties, making it a valuable research tool across multiple scientific disciplines. As a synthetic molecule with a defined glycosidic architecture, it offers a consistent platform for experimental reproducibility and mechanistic studies. The compound's solubility profile and functional group accessibility allow for straightforward integration into various experimental protocols. Its stability under a range of laboratory conditions enables researchers to design complex assays without concerns about rapid degradation or unwanted side reactions. The molecular configuration of CID 162678814 has been engineered to mimic certain natural carbohydrate motifs, lending itself to applications that require biomimicry or the investigation of carbohydrate-mediated interactions.
Glycobiology Research: CID 162678814 serves as an essential probe in glycobiology, where it facilitates the study of carbohydrate-protein interactions, glycan recognition, and enzymatic processing of oligosaccharides. Scientists employ the compound to map the binding specificity of lectins and glycosyltransferases, advancing the understanding of cellular communication and signaling pathways mediated by carbohydrates. Its defined structure allows for controlled experiments that dissect the roles of specific glycosidic linkages in biological systems, helping to elucidate the mechanisms underlying cell adhesion, immune modulation, and pathogen recognition. The use of this compound in model systems accelerates the identification of potential carbohydrate motifs involved in disease progression or immune response.
Enzyme Substrate Characterization: In enzymology, the synthetic carbohydrate acts as a substrate analogue for the detailed characterization of glycosidases and glycosyltransferases. By providing a consistent and pure substrate, it enables kinetic studies that reveal enzyme specificity, catalytic efficiency, and substrate preferences. Researchers can use CID 162678814 to design assays that monitor the formation or cleavage of glycosidic bonds, thereby illuminating the catalytic mechanisms of enzymes involved in carbohydrate metabolism. Such insights are critical for understanding metabolic pathways, engineering novel biocatalysts, or developing inhibitors that target specific enzymatic steps.
Analytical Method Development: Analytical chemists utilize the compound as a standard or calibration reference in the development and validation of carbohydrate detection methods. Its well-defined structure and predictable chromatographic behavior make it ideal for optimizing high-performance liquid chromatography (HPLC), mass spectrometry, and capillary electrophoresis protocols. The inclusion of CID 162678814 in method development workflows ensures accurate quantification and identification of carbohydrates in complex biological or environmental samples. The compound's stability and detectability enhance the reliability of analytical results, supporting robust quality control and traceability in research and industrial settings.
Chemical Synthesis and Modification: The molecule's accessible functional groups and modular structure render it an excellent starting material or intermediate in the synthesis of more complex oligosaccharides and glycoconjugates. Organic chemists exploit its reactivity to introduce specific modifications, such as labeling with fluorescent tags or attachment to solid supports for affinity purification. The versatility of CID 162678814 in synthetic schemes enables the generation of carbohydrate libraries for screening studies or the creation of novel biomaterials with tailored properties. Its use in combinatorial synthesis accelerates the discovery of new bioactive molecules and the development of innovative research tools.
Biomaterials and Surface Engineering: Researchers in the field of biomaterials leverage the compound to design carbohydrate-coated surfaces or hydrogels that mimic the extracellular matrix. By immobilizing CID 162678814 on various substrates, scientists create model systems to study cell-surface interactions, tissue engineering, and the effects of carbohydrate presentation on cellular behavior. These engineered surfaces facilitate investigations into stem cell differentiation, wound healing, and the development of biosensors sensitive to glycan-binding proteins. The molecule's compatibility with diverse materials and surface chemistries expands its utility in the fabrication of advanced biomedical devices and diagnostic platforms.
Immunological Assays: In immunology research, CID 162678814 is incorporated into assay systems to examine antibody specificity, antigen recognition, and the role of carbohydrate antigens in immune responses. The compound's defined structure allows for the generation of precise immunoassays that differentiate between closely related glycan epitopes, supporting the development of highly selective detection reagents. Its use in multiplexed platforms enables the simultaneous analysis of multiple carbohydrate-antibody interactions, advancing the understanding of immune recognition and the identification of novel biomarkers. By providing a reliable and reproducible glycan standard, CID 162678814 contributes to the accuracy and sensitivity of immunological investigations, furthering progress in fundamental and applied research.
3. Immune responses to homocitrulline-and citrulline-containing peptides in rheumatoid arthritis
4. An Open-label, Single-center, Safety and Efficacy Study of Eyelash Polygrowth Factor Serum
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