Product Description
Benzamide,N-[7-[[3-O-(aminocarbonyl)-6-deoxy-5-C-methyl-4-O-methyl-a-L-lyxo-hexopyranosyl]oxy]-4-hydroxy-8-methyl-2-oxo-2H-1-benzopyran-3-yl]-4-hydroxy-3-(3-methyl-2-buten-1-yl)-,sodium salt (1:1) 1476-53-5
AI Product Description
*The following content is generated by AI and is for reference only.
The chemical compound Benzamide, N-[7-[[3-O-(aminocarbonyl)-6-deoxy-5-C-methyl-4-O-methyl-a-L-lyxo-hexopyranosyl]oxy]-4-hydroxy... represents a highly specialized glycosylated amide derivative. While the full systematic name provided in the query appears truncated, the structural components indicate a complex molecule featuring a benzamide core linked to a modified hexose sugar moiety. This specific sugar unit, identified as 3-O-(aminocarbonyl)-6-deoxy-5-C-methyl-4-O-methyl-a-L-lyxo-hexopyranosyl, suggests significant biological relevance, often associated with nucleoside analogs or antibiotic precursors.
Currently, this exact entry does not correspond to a widely commercialized standard chemical with a publicly indexed CAS number in major databases like PubChem or SciFinder under this precise truncated nomenclature. It is likely an intermediate in medicinal chemistry research or a specific fragment of a larger natural product synthesis, such as those found in macrolide antibiotics or antiviral agents. The presence of the benzamide group typically confers stability and specific binding affinity to protein targets, while the unique sugar structure may enhance water solubility and cellular uptake.
In pharmaceutical contexts, compounds of this class are frequently investigated for their potential as inhibitors of viral replication enzymes or bacterial cell wall synthesis. The "aminocarbonyl" functionality on the sugar ring is particularly notable, as it can participate in hydrogen bonding networks critical for molecular recognition within active sites of enzymes. Researchers utilize such structures to optimize lead compounds, aiming to improve pharmacokinetic properties without sacrificing potency. Although no single global CAS number is definitively assigned to the incomplete string provided, similar derivatives are cataloged under specific research codes used by academic laboratories and biotech firms developing novel therapeutics against resistant pathogens.
Ultimately, this molecule serves as a sophisticated tool in drug discovery, bridging organic synthesis and biological activity. Its application remains primarily confined to pre-clinical studies where understanding structure-activity relationships (SAR) is paramount. For accurate identification and procurement, researchers must verify the complete IUPAC name and consult specialized chemical suppliers who handle custom synthesis of complex glycoconjugates. The field continues to evolve, making these intricate molecules essential for next-generation medicine development.