Date published: 2026-9-2

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N-ε-Aminocaproyl-β-D-galactopyranosylamine (CAS 38822-56-9)

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Application:
N-ε-Aminocaproyl-β-D-galactopyranosylamine is used for the preparation of sugar specific antibodies
CAS Number:
38822-56-9
Molecular Weight:
292.33
Molecular Formula:
C12H24N2O6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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N-ε-Aminocaproyl-β-D-galactopyranosylamine is a chemical compound of significant interest in glycobiology research due to its role as a key intermediate in the synthesis of various glycoconjugates and glycomimetics. Its mechanism of action lies in its ability to serve as a building block for the construction of complex carbohydrates and glycoconjugates with specific biological activities. Researchers utilize this compound in the synthesis of glycan structures with defined sequences and functionalities, allowing for the investigation of glycan-protein interactions, cell adhesion processes, and immune responses. Moreover, N-ε-Aminocaproyl-β-D-galactopyranosylamine serves as a precursor for the preparation of neoglycoconjugates and glycosylated biomaterials used in biophysical studies, bioconjugation chemistry, and glycoengineering applications. Its incorporation into glycans enables researchers to modulate glycan structure and function, facilitating the study of carbohydrate-mediated signaling pathways and cellular processes. Additionally, N-ε-Aminocaproyl-β-D-galactopyranosylamine finds utility in the development of glycan-based probes and biosensors, contributing to advancements in drug delivery, diagnostics, and biomaterial design. Overall, this chemical compound plays a pivotal role in advancing our understanding of carbohydrate biology and has broad applications in research fields such as glycobiology, biochemistry, and biomedical engineering.


N-ε-Aminocaproyl-β-D-galactopyranosylamine (CAS 38822-56-9) References

  1. Structure-based exploration of the ganglioside GM1 binding sites of Escherichia coli heat-labile enterotoxin and cholera toxin for the discovery of receptor antagonists.  |  Minke, WE., et al. 1999. Biochemistry. 38: 5684-92. PMID: 10231518
  2. Analysis of surface properties of fixed and live cells using derivatized agarose beads.  |  Navarro, VM., et al. 2002. Acta Histochem. 104: 99-106. PMID: 11993857
  3. Solution and crystallographic studies of branched multivalent ligands that inhibit the receptor-binding of cholera toxin.  |  Zhang, Z., et al. 2002. J Am Chem Soc. 124: 12991-8. PMID: 12405825
  4. Nonspanning bivalent ligands as improved surface receptor binding inhibitors of the cholera toxin B pentamer.  |  Pickens, JC., et al. 2004. Chem Biol. 11: 1205-15. PMID: 15380181
  5. Interpreting steep dose-response curves in early inhibitor discovery.  |  Shoichet, BK. 2006. J Med Chem. 49: 7274-7. PMID: 17149857

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

N-ε-Aminocaproyl-β-D-galactopyranosylamine, 5 mg

sc-221965
5 mg
$320.00