Date published: 2026-1-20

1-800-457-3801

SCBT Portrait Logo
Seach Input

4-Nitrophenyl β-D-mannopyranoside (CAS 35599-02-1)

0.0(0)
Write a reviewAsk a question

Alternate Names:
p-Nitrophenyl β-D-mannopyranoside
Application:
4-Nitrophenyl β-D-mannopyranoside is a glycoside for proteomics research
CAS Number:
35599-02-1
Purity:
≥97%
Molecular Weight:
301.25
Molecular Formula:
C12H15NO8
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

4-Nitrophenyl β-D-mannopyranoside consists of a β-D-mannopyranose molecule, which is a form of mannose, a sugar, that is in the pyranose ring form. The sugar is linked to a nitrophenyl group, specifically the 4-position of the phenyl ring is substituted with a nitro group (-NO2). This structural feature imparts distinctive chemical properties to the molecule, including its reactivity and interactions with other substances. It is of interest primarily in the fields of biochemistry and organic chemistry, where it may be used as a reagent or a substrate in various chemical reactions or as a part of synthetic pathways. Its specific structure, incorporating both a sugar component and a nitro-aromatic moiety, enables it to participate in a variety of chemical processes, including those that involve enzymatic reactions or serve as a model compound for studying the interactions between enzymes and substrates. Furthermore, 4-Nitrophenyl β-D-mannopyranoside can be used in analytical chemistry as a chromogenic substrate. When enzymatically cleaved, it can release a 4-nitrophenol moiety, which is easily detectable by spectroscopic methods due to its absorbance in the visible range, allowing for the monitoring of enzymatic activity in various research applications.


4-Nitrophenyl β-D-mannopyranoside (CAS 35599-02-1) References

  1. Directed evolution of a glycosynthase from Agrobacterium sp. increases its catalytic activity dramatically and expands its substrate repertoire.  |  Kim, YW., et al. 2004. J Biol Chem. 279: 42787-93. PMID: 15252054
  2. Glycosylation of bisphenol A by freshwater microalgae.  |  Nakajima, N., et al. 2007. Chemosphere. 69: 934-41. PMID: 17629547
  3. Rice family GH1 glycoside hydrolases with beta-D-glucosidase and beta-D-mannosidase activities.  |  Kuntothom, T., et al. 2009. Arch Biochem Biophys. 491: 85-95. PMID: 19766588
  4. Synthesis of some D-mannosyl-oligosaccharides containing the methyl and 4-nitrophenyl beta-D-mannopyranoside units.  |  Khan, SH., et al. 1990. Carbohydr Res. 207: 57-69. PMID: 2076513
  5. Purification and characterization of a Ca(2+)-dependent novel lectin from Nymphaea nouchali tuber with antiproliferative activities.  |  Kabir, SR., et al. 2011. Biosci Rep. 31: 465-75. PMID: 21291421
  6. A new lectin from the tuberous rhizome of Kaempferia rotunda: isolation, characterization, antibacterial and antiproliferative activities.  |  Kabir, SR., et al. 2011. Protein Pept Lett. 18: 1140-9. PMID: 21707523
  7. Mutations in the substrate entrance region of β-glucosidase from Trichoderma reesei improve enzyme activity and thermostability.  |  Lee, HL., et al. 2012. Protein Eng Des Sel. 25: 733-40. PMID: 23077275
  8. Characterization of the α- and β-mannosidases of Porphyromonas gingivalis.  |  Rangarajan, M., et al. 2013. J Bacteriol. 195: 5297-307. PMID: 24056103
  9. The Bitter Taste Receptor TAS2R16 Achieves High Specificity and Accommodates Diverse Glycoside Ligands by using a Two-faced Binding Pocket.  |  Thomas, A., et al. 2017. Sci Rep. 7: 7753. PMID: 28798468
  10. Glycoside hydrolase DisH from Desulfovibrio vulgaris degrades the N-acetylgalactosamine component of diverse biofilms.  |  Zhu, L., et al. 2018. Environ Microbiol. 20: 2026-2037. PMID: 29411481
  11. Characterization of mannanase from Bacillus sp., a novel Codium fragile cell wall-degrading bacterium.  |  Kim, S., et al. 2018. Food Sci Biotechnol. 27: 115-122. PMID: 30263731
  12. Geodorum densiflorum rhizome lectin inhibits Ehrlich ascites carcinoma cell growth by inducing apoptosis through the regulation of BAX, p53 and NF-κB genes expression.  |  Ahsanul Kabir, KM., et al. 2019. Int J Biol Macromol. 125: 92-98. PMID: 30521911
  13. Structure and biochemical characterization of glucose tolerant β-1,4 glucosidase (HtBgl) of family 1 glycoside hydrolase from Hungateiclostridium thermocellum.  |  Sharma, K., et al. 2019. Carbohydr Res. 483: 107750. PMID: 31357130
  14. Hydrolase-catalyzed beta-mannosylations.  |  Taubken, N. and Thiem, J. 1998. Glycoconj J. 15: 757-67. PMID: 9870351

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Nitrophenyl β-D-mannopyranoside, 25 mg

sc-220972
25 mg
$134.00

4-Nitrophenyl β-D-mannopyranoside, 100 mg

sc-220972A
100 mg
$437.00