Date published: 2026-2-2

1-800-457-3801

SCBT Portrait Logo
Seach Input

3α,6α-Mannopentaose (CAS 112828-69-0)

0.0(0)
Write a reviewAsk a question

See product citations (1)

Alternate Names:
α-Man-(1→3)(α-Man-[1→6])-α-Man-(1→6)(α-Man-[1→3])-Man
Application:
3α,6α-Mannopentaose is a core structure of some triantennary N-linked oligosaccharides
CAS Number:
112828-69-0
Molecular Weight:
828.72
Molecular Formula:
C30H52O26
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

3α,6α-Mannopentaose, a complex oligosaccharide derived from mannose, has emerged as a crucial tool in glycobiology research due to its structural significance and functional roles. This compound serves as a model system for studying carbohydrate-protein interactions, particularly those involving lectins and carbohydrate-binding proteins. Its unique branched structure and specific glycosidic linkages enable investigations into the recognition and binding properties of carbohydrate-binding proteins, shedding light on molecular recognition events crucial for cellular processes such as cell adhesion, signaling, and immune response modulation. Moreover, 3α,6α-Mannopentaose has been instrumental in elucidating the molecular mechanisms underlying pathogen-host interactions, particularly in microbial adhesion and biofilm formation. By studying the interaction of this oligosaccharide with microbial adhesins and lectins, researchers gain insights into strategies for developing targets for bacterial and fungal infections. Furthermore, 3α,6α-Mannopentaose serves as a substrate for enzymatic assays and glycosylation studies, facilitating the characterization of glycosyltransferases and glycosidases involved in carbohydrate biosynthesis and degradation pathways. Its multifaceted roles in carbohydrate chemistry and glycobiology highlight its significance as a valuable research tool for investigating diverse biological processes and developing novel strategies for intervention.


3α,6α-Mannopentaose (CAS 112828-69-0) References

  1. 3-Aminoquinoline acting as matrix and derivatizing agent for MALDI MS analysis of oligosaccharides.  |  Rohmer, M., et al. 2010. Anal Chem. 82: 3719-26. PMID: 20387804
  2. Voltammetric determination of Os(VI)-modified oligosaccharides at nanomolar level.  |  Trefulka, M. and Paleček, E. 2012. Bioelectrochemistry. 88: 8-14. PMID: 22763419
  3. Burkholderia oklahomensis agglutinin is a canonical two-domain OAA-family lectin: structures, carbohydrate binding and anti-HIV activity.  |  Whitley, MJ., et al. 2013. FEBS J. 280: 2056-67. PMID: 23480609
  4. Ion mobility-mass spectrometry of intact protein--ligand complexes for pharmaceutical drug discovery and development.  |  Niu, S., et al. 2013. Curr Opin Chem Biol. 17: 809-17. PMID: 23856053
  5. Sampling of Glycan-Bound Conformers by the Anti-HIV Lectin Oscillatoria agardhii agglutinin in the Absence of Sugar.  |  Carneiro, MG., et al. 2015. Angew Chem Int Ed Engl. 54: 6462-5. PMID: 25873445
  6. Atmospheric pressure neutral reionization mass spectrometry for structural analysis.  |  Liu, P., et al. 2017. Chem Sci. 8: 6499-6507. PMID: 28989675
  7. Structural investigation of glycan recognition by the ERAD quality control lectin Yos9.  |  Kniss, A., et al. 2018. J Biomol NMR. 72: 1-10. PMID: 30066206
  8. Fast and Sensitive Detection of Oligosaccharides Using Desalting Paper Spray Mass Spectrometry (DPS-MS).  |  Wang, Q., et al. 2020. J Am Soc Mass Spectrom. 31: 2226-2235. PMID: 32910855
  9. Molecularly imprinted materials for glycan recognition and processing.  |  Zhao, Y. 2022. J Mater Chem B. 10: 6607-6617. PMID: 35481837
  10. Targeting spike glycans to inhibit SARS-CoV2 viral entry.  |  Guseman, AJ., et al. 2023. Proc Natl Acad Sci U S A. 120: e2301518120. PMID: 37695910

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3α,6α-Mannopentaose, 5 mg

sc-256602
5 mg
$220.00