Nojirimycin Bisulfite

• Description:

  Nojirimycin Bisulfite Catalog number: MDP0889 Lot number: Batch Dependent Expiration Date: Batch dependent Amount: 1 mg Molecular Weight or Concentration: 243.23 g/mol Supplied as: Powder Applications: potent inhibitor of glucosidase Storage: -20°C Keywords: 5-Amino-5-Deoxy-Glucopyranose Bisulfite, Nojirimycin 1-sulfonic acid Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um. Indication for Use: This product is for Research Use Only. This product is NOT for human or animal use. References: 1: Hyun SB, Chung YC, Hyun C-. Nojirimycin suppresses inflammation via regulation of NF-κ B signaling pathways. Pharmazie. 2020 Dec 1;75(12):637-641. 2: Okazawa A, Wakabayashi T, Muranaka T, Sugimoto Y, Ohta D. The effect of nojirimycin on the transcriptome of germinating Orobanche minor seeds. J Pestic Sci. 2020 Nov 20;45(4):230-237. 3: Cuffaro D, Landi M, D'Andrea F, Guazzelli L. Preparation of 1,6-di-deoxy-d- galacto and 1,6-di-deoxy-l-altro nojirimycin derivatives by aminocyclization of a 1,5-dicarbonyl derivative. Carbohydr Res. 2019 Aug 1;482:107744. 4: Tsuruoka T, Fukuyasu H, Ishii M, Usui T, Shibahara S, Inouye S. Inhibition of mouse tumor metastasis with nojirimycin-related compounds. J Antibiot (Tokyo). 1996 Feb;49(2):155-61. 5: Viuff AH, Besenbacher LM, Kamori A, Jensen MT, Kilian M, Kato A, Jensen HH. Stable analogues of nojirimycin--synthesis and biological evaluation of nojiristegine and manno-nojiristegine. Org Biomol Chem. 2015 Oct 7;13(37):9637-58. 6: Bini D, Cardona F, Forcella M, Parmeggiani C, Parenti P, Nicotra F, Cipolla L. Synthesis and biological evaluation of nojirimycin- and pyrrolidine-based trehalase inhibitors. Beilstein J Org Chem. 2012;8:514-21. 7: Chambers JP, Elbein AD, Williams JC. Nojirimycin-a potent inhibitor of purified lysosomal alpha-glucosidase from human liver. Biochem Biophys Res Commun. 1982 Aug 31;107(4):1490-6. 8: Harada K, Kurono Y, Nagasawa S, Oda T, Nasu Y, Wakabayashi T, Sugimoto Y, Matsuura H, Muranaka S, Hirata K, Okazawa A. Enhanced production of nojirimycin viaStreptomyces ficellus cultivation using marine broth and inhibitory activity of the culture for seeds of parasitic weeds. J Pestic Sci. 2017 Nov 24;42(4):166-171. 9: Brumshtein B, Aguilar-Moncayo M, Benito JM, García Fernandez JM, Silman I, Shaaltiel Y, Aviezer D, Sussman JL, Futerman AH, Ortiz Mellet C. Cyclodextrin- mediated crystallization of acid β-glucosidase in complex with amphiphilic bicyclic nojirimycin analogues. Org Biomol Chem. 2011 Jun 7;9(11):4160-7.
  Products Related to Nojirimycin Bisulfite : Peptides

• Short Description:

  Catalog Number: MDP0889 (1 mg)

• Weight:

  0.15

• Length:

  2

• Width:

  0.5

• Height:

  0.5

• Height :

  0.5