Date published: 2026-6-8

1-800-457-3801

SCBT Portrait Logo
Seach Input

3′-Sulfated Lewis A (CAS 153088-71-2)

0.0(0)
Write a reviewAsk a question

CAS Number:
153088-71-2
Molecular Weight:
609.55
Molecular Formula:
C20H35NO18S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Phosphatidyl-L-serine (PS) is a phospholipid component crucial to the structure and function of biological membranes, particularly in the brain and nervous system. Structurally, it consists of two fatty acid chains linked to a glycerol backbone, with one of the hydroxyl groups of glycerol esterified to phosphoric acid, which is further linked to the amino acid serine. This configuration imparts specific biophysical properties to membranes, including fluidity and phase behavior, which are essential for proper cellular function. In research contexts, PS is often studied for its role in signaling pathways associated with apoptosis (programmed cell death) and cellular signaling. The presence of PS on the inner leaflet of the cell membrane′s bilayer is pivotal in maintaining cellular integrity and signaling cascades. However, during apoptosis, PS is translocated to the outer leaflet, where it serves as a signal for phagocytes to engulf apoptotic cells, a process vital for tissue homeostasis and immune response. In scientific studies, PS has been used as a tool to understand membrane asymmetry and the mechanisms underlying apoptosis, without therapeutic intent. Researchers utilize it in a variety of experimental setups, including artificial membrane systems and live cell imaging, to track and manipulate cellular processes under controlled conditions, thereby elucidating the complex interactions of cellular signaling networks. Such studies provide foundational knowledge that can inform broader biological and biochemical insights.


3′-Sulfated Lewis A (CAS 153088-71-2) References

  1. Chemoenzymatic synthesis of the 3-sulfated Lewisa pentasaccharide.  |  Malleron, A., et al. 2006. Carbohydr Res. 341: 29-34. PMID: 16274756
  2. Carbohydrate antigen sialyl Lewis a--its pathophysiological significance and induction mechanism in cancer progression.  |  Kannagi, R. 2007. Chang Gung Med J. 30: 189-209. PMID: 17760270
  3. Chemo-enzymatic supported synthesis of the 3-sulfated Lewis a pentasaccharide on a multimeric polyethylene glycol.  |  Malleron, A. and Le Narvor, C. 2008. Carbohydr Res. 343: 970-6. PMID: 18280461
  4. 3'-Sulfo-Le(x) is important for regulation of integrin subunit alphaV.  |  Zhang, CY., et al. 2010. Biochemistry. 49: 7811-20. PMID: 20695481
  5. Evidence for a lectin specific for sulfated glycans in the salivary gland of the malaria vector, Anopheles gambiae.  |  Francischetti, IM., et al. 2014. PLoS One. 9: e107295. PMID: 25207644
  6. 3'-sulfated LewisA/C: An oncofetal epitope associated with metaplastic and oncogenic plasticity of the gastrointestinal foregut.  |  Das, KK. and Brown, JW. 2023. Front Cell Dev Biol. 11: 1089028. PMID: 36866273
  7. Unveiling the Potential of Extracellular Vesicles as Biomarkers and Therapeutic Nanotools for Gastrointestinal Diseases.  |  Arrè, V., et al. 2024. Pharmaceutics. 16: PMID: 38675228
  8. First synthesis of the 3'-sulfated Lewis(a) pentasaccharide, the most potent human E-selectin ligand so far.  |  Lubineau, A., et al. 1994. Bioorg Med Chem. 2: 1143-51. PMID: 7538868
  9. Prevention of ischemia-reperfusion lung injury by sulfated Lewis(a) pentasaccharide. The Paris-Sud University Lung Transplantation Group.  |  Reignier, J., et al. 1997. J Appl Physiol (1985). 82: 1058-63. PMID: 9104839
  10. Novel carbohydrate specificity of monoclonal antibody 91.9H prepared against human colonic sulfomucin: recognition of sulfo-Lewis(a) structure.  |  Tsuiji, H., et al. 1998. Biochem Biophys Res Commun. 253: 374-81. PMID: 9878545

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3'-Sulfated Lewis A, 250 µg

sc-283952
250 µg
$425.00

3'-Sulfated Lewis A, 500 µg

sc-283952A
500 µg
$650.00