Date published: 2025-12-5

1-800-457-3801

SCBT Portrait Logo
Seach Input

Deoxymannojirimycin hydrochloride (CAS 84444-90-6)

0.0(0)
Write a reviewAsk a question

See product citations (2)

Alternate Names:
DMJ
Application:
Deoxymannojirimycin hydrochloride is a mannose analog that inhibits mammalian Golgi-α-mannosidase I
CAS Number:
84444-90-6
Purity:
≥98%
Molecular Weight:
199.6
Molecular Formula:
C6H13NO4•HCl
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Deoxymannojirimycin hydrochloride (DMJ-HCl) is a synthetic analogue of the naturally occurring alkaloid mannojirimycin. It belongs to a class of compounds known as iminosugars or glycosidase inhibitors. This chemical is structurally similar to D-mannose and primarily acts by inhibiting alpha-mannosidases, enzymes responsible for cleaving mannose residues from glycoproteins and glycolipids. This inhibition disrupts the processing and maturation of N-linked oligosaccharides in the Golgi apparatus of cells. DMJ-HCl has been utilized extensively as a tool to study the role and mechanism of glycosidases in the post-translational modification of proteins. By blocking alpha-mannosidase activity, researchers are able to investigate the pathways involved in the synthesis and modification of glycoproteins, particularly how these processes affect protein folding, trafficking, and function within the cell. Further, the use of DMJ-HCl in research has helped explain the biosynthesis of glycoproteins and the pathogenesis of disorders related to glycoprotein processing abnormalities. Studies involving DMJ-HCl have contributed to a deeper understanding of various cellular mechanisms, including those linked to developmental biology and cellular communication. Through these investigations, DMJ-HCl has proven to be an invaluable agent in exploring fundamental biological processes and the molecular basis of enzyme function.


Deoxymannojirimycin hydrochloride (CAS 84444-90-6) References

  1. C-type lectins L-SIGN and DC-SIGN capture and transmit infectious hepatitis C virus pseudotype particles.  |  Lozach, PY., et al. 2004. J Biol Chem. 279: 32035-45. PMID: 15166245
  2. 1-Deoxymannojirimycin, the alpha1,2-mannosidase inhibitor, induced cellular endoplasmic reticulum stress in human hepatocarcinoma cell 7721.  |  Lu, Y., et al. 2006. Biochem Biophys Res Commun. 344: 221-5. PMID: 16615997
  3. Acquisition of complement resistance through incorporation of CD55/decay-accelerating factor into viral particles bearing baculovirus GP64.  |  Kaname, Y., et al. 2010. J Virol. 84: 3210-9. PMID: 20071581
  4. Hiding inside? Intracellular expression of non-glycosylated c-kit protein in cardiac progenitor cells.  |  Shi, H., et al. 2016. Stem Cell Res. 16: 795-806. PMID: 27161312
  5. The use of 1-deoxymannojirimycin to evaluate the role of various alpha-mannosidases in oligosaccharide processing in intact cells.  |  Bischoff, J., et al. 1986. J Biol Chem. 261: 4766-74. PMID: 2937779
  6. Secretion of high-mannose-type alpha 1-proteinase inhibitor and alpha 1-acid glycoprotein by primary cultures of rat hepatocytes in the presence of the mannosidase I inhibitor 1-deoxymannojirimycin.  |  Gross, V., et al. 1985. Eur J Biochem. 150: 41-6. PMID: 3160588
  7. A role for N-glycosylation in active adenosine deaminase 2 production.  |  Ito, M., et al. 2022. Biochim Biophys Acta Gen Subj. 1866: 130237. PMID: 36029899
  8. Effect of retinyl acetate on the assembly of the fibronectin extracellular matrix and the processing of the fibronectin receptor beta subunit of confluent C3H/10T1/2 mouse embryo fibroblasts.  |  Suzuki, SS. and Piette, LH. 1993. J Cell Biochem. 51: 181-9. PMID: 8440752
  9. Glycosylation of native MHC class Ia molecules is required for recognition by allogeneic cytotoxic T lymphocytes.  |  Bagriaçik, EU., et al. 1996. Glycobiology. 6: 413-21. PMID: 8842705
  10. Studies on the site and mechanism of attachment of phosphorylcholine to a filarial nematode secreted glycoprotein.  |  Houston, KM., et al. 1997. J Biol Chem. 272: 1527-33. PMID: 8999824

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Deoxymannojirimycin hydrochloride, 1 mg

sc-201360
1 mg
$93.00

Deoxymannojirimycin hydrochloride, 5 mg

sc-201360A
5 mg
$239.00