DA-61292

DA-61292 offers a peptide-derived scaffold suited for exploring structural determinants of binding interactions. Its residue diversity creates a balanced hydrophobic-polar landscape. Researchers investigate conformational states across solvent systems. Applications extend to ligand optimization, sequence-function studies, and receptor-modeling research.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
DA-61292(CAS 1402453-15-9)

CAT No: R2433

CAS No:1402453-15-9

Synonyms/Alias:1402453-15-9;DA-61292;(2S)-2-acetamido-5-(diaminomethylideneamino)-N-[(2S)-2-(diethylamino)-3-(4-nitrophenyl)propanoyl]pentanamide;

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  • Drug master files (DMF) filing
M.F/Formula
C21H33N7O5
M.W/Mr.
463.5

DA-61292 is a specialized carbohydrate compound recognized for its unique structural properties and versatile reactivity, making it a valuable asset in scientific research and industrial development. Distinguished by its well-defined stereochemistry, DA-61292 serves as an essential building block for the synthesis of complex oligosaccharides and glycoconjugates. Its compatibility with a range of chemical modification techniques allows researchers to tailor its molecular features for specific experimental needs. The compound's solubility profile and stability under various conditions further enhance its applicability in both aqueous and organic environments, supporting a broad spectrum of research methodologies. By integrating seamlessly into diverse synthetic pathways, DA-61292 enables the advancement of carbohydrate chemistry and the exploration of novel biomolecular interactions.

Glycobiology Research: DA-61292 is widely employed in glycobiology to elucidate the roles of carbohydrates in cellular communication, molecular recognition, and signal transduction. Its defined structure enables the precise modeling of glycan interactions with proteins, facilitating the study of lectin binding and glycan-mediated signaling events. Researchers utilize this compound to construct glycan arrays and probe the specificity of carbohydrate-binding proteins, advancing the understanding of cellular processes governed by glycosylation. By serving as a model substrate, it supports investigations into the biosynthesis and functional implications of complex glycans, providing insights into fundamental biological mechanisms.

Synthetic Chemistry: In the field of synthetic organic chemistry, DA-61292 functions as a key intermediate for the assembly of structurally diverse oligosaccharides and carbohydrate-based polymers. Its reactivity allows for the introduction of protective groups, branching points, and functional modifications, enabling the stepwise construction of tailored carbohydrate architectures. Chemists leverage its versatility to generate libraries of glycomimetics and designer glycans for structure-activity relationship studies. The compound's robust performance in glycosylation reactions streamlines the synthesis of target molecules, supporting the development of novel materials and bioactive compounds.

Bioconjugation and Probe Development: As a functionalizable carbohydrate scaffold, DA-61292 is instrumental in the design of bioconjugates and molecular probes. Its multiple reactive sites permit the attachment of fluorescent tags, affinity labels, or therapeutic agents, facilitating the creation of specialized tools for biomolecular detection and imaging. Researchers exploit its compatibility with click chemistry and other ligation strategies to develop probes that selectively target glycan-binding proteins or cellular receptors. This application enhances the ability to trace carbohydrate dynamics in complex biological systems and supports the development of innovative diagnostic technologies.

Material Science: The distinctive properties of DA-61292 make it valuable in the development of carbohydrate-based materials with tailored physicochemical characteristics. Its incorporation into hydrogels, nanoparticles, or surface coatings imparts biocompatibility, tunable degradation rates, and specific recognition capabilities. Material scientists utilize this compound to engineer smart materials for biosensing, controlled release, or tissue engineering applications. By modulating its molecular interactions, it is possible to create advanced materials that respond dynamically to environmental stimuli or biological signals.

Enzymology and Enzyme Engineering: DA-61292 is frequently used as a substrate or inhibitor in enzymology studies to investigate the specificity and catalytic mechanisms of glycosidases and glycosyltransferases. Its defined structure allows for the assessment of enzyme-substrate interactions, kinetic analyses, and the screening of enzyme variants. Enzyme engineers employ this compound to design and optimize biocatalysts for carbohydrate synthesis, degradation, or modification. The insights gained from these studies contribute to the development of efficient enzymatic processes for industrial biotechnology and the synthesis of structurally complex carbohydrates.

By supporting a wide array of research directions, DA-61292 continues to advance the frontiers of carbohydrate science. Its multifaceted applications in glycobiology, synthetic chemistry, probe development, material science, and enzymology underscore its importance as a foundational reagent in modern research. As scientists explore new frontiers in glycoscience, this compound remains a catalyst for innovation, enabling the design of sophisticated biomolecules, functional materials, and analytical tools that address emerging challenges in the life and physical sciences.

InChI
InChI=1S/C21H33N7O5/c1-4-27(5-2)18(13-15-8-10-16(11-9-15)28(32)33)20(31)26-19(30)17(25-14(3)29)7-6-12-24-21(22)23/h8-11,17-18H,4-7,12-13H2,1-3H3,(H,25,29)(H4,22,23,24)(H,26,30,31)/t17-,18-/m0/s1
InChI Key
VTJQHXSKCSNQTD-ROUUACIJSA-N

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