N-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-undec-10-enoxyoxan-3-yl]acetamide

N-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-undec-10-enoxyoxan-3-yl]acetamide

N-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-undec-10-enoxyoxan-3-yl]acetamide (CAS No. 262363-70-2) is a complex glycosylated compound with significant relevance in biochemical research and potential pharmaceutical applications. This compound is characterized by its unique structure, which includes multiple hydroxyl groups and an acetamide functional group, making it a valuable substrate for studying glycosylation processes and enzyme interactions.

Chemical Properties

• CAS Number: 262363-70-2
• MDL Number: MFCD29067177
• EINECS: Not available
• Molecular Formula: C19H35NO6
• Molecular Weight: 373.48 g/mol
• Boiling Point: Not specified
• Melting Point: Not specified

Structure and Composition

The structure of N-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-undec-10-enoxyoxan-3-yl]acetamide features several key components:

1. Oxan Sugar Backbone: The oxan structure provides a carbohydrate framework essential for biological recognition and interaction with enzymes.
2. Hydroxymethyl and Hydroxyl Groups: The presence of multiple hydroxyl groups enhances the compound’s solubility and reactivity, allowing it to participate in various chemical reactions.
3. Acetamide Group: The acetamide moiety contributes to the compound’s stability and can influence its biological activity.
4. Double Bond: The presence of a double bond in the undec-10-enoxy chain adds to the compound’s structural complexity and potential reactivity.

Applications

N-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-undec-10-enoxyoxan-3-yl]acetamide is utilized in several applications:

Biochemical Research

1. Glycosylation Studies: This compound serves as a substrate for glycosyltransferases, enabling researchers to investigate glycosylation pathways and enzyme kinetics.
2. Enzymatic Assays: It can be employed in assays to measure the activity of specific enzymes involved in carbohydrate metabolism.

Pharmaceutical Development

1. Drug Design: Its unique structural features make it a candidate for developing glycosylated drugs that require specific targeting mechanisms or enhanced bioactivity.

Safety and Handling

While specific safety data for this compound are not extensively documented, standard laboratory safety practices should be followed:

1. Personal Protective Equipment (PPE): Use gloves, goggles, and lab coats when handling this compound to avoid skin or eye contact.
2. Ventilation: Work in a well-ventilated area or fume hood to minimize exposure to vapors or dust.
3. Storage Conditions: Store the compound at temperatures between 2 to 8 °C to maintain stability.
4. Disposal Guidelines: Dispose of waste according to local regulations regarding hazardous materials.

Summary

In summary, N-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-undec-10-enoxyoxan-3-yl]acetamide (CAS No. 262363-70-2) is an important reagent in biochemical research for studying glycosylation processes and facilitating enzymatic assays. Its unique structural features enable its use in drug development and other applications within carbohydrate chemistry.

Citations:

1. https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI%3A157386
2. https://www.benchchem.com/product/b164939
3. https://pubchem.ncbi.nlm.nih.gov/compound/5288888
4. https://pubchem.ncbi.nlm.nih.gov/compound/49835811
5. https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI%3A146117
6. https://www.molport.com/shop/compound/Molport-000-729-233
7. https://www.molport.com/shop/compound/Molport-046-683-650
8. https://smallmolecules.com/product/135608-48-9-chemscene-n-2s3r4r5s6r-2-4-formylphenoxy-45-dihydroxy-6-hydroxymethyltetrahydro-2h-pyran-3-ylacetamide-chemscene-1g/