Nojirimycin Bisulfite

<strong>Nojirimycin Bisulfite</strong> <strong>Catalog number:</strong> MDP0889 <strong>Lot number:</strong> Batch Dependent <strong>Expiration Date:</strong> Batch dependent <strong>Amount:</strong> 1 mg <strong>Molecular Weight or Concentration:</strong> 243.23 g/mol <strong>Supplied as:</strong> Powder <strong>Applications:</strong> potent inhibitor of glucosidase <strong>Storage:</strong> -20°C <strong>Keywords:</strong> 5-Amino-5-Deoxy-Glucopyranose Bisulfite, Nojirimycin 1-sulfonic acid <strong>Grade:</strong> 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. <strong>Indication for Use: </strong>This product is for Research Use Only. This product is NOT for human or animal use. <strong>References:</strong> 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 <i>Orobanche minor</i> 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 <i>via</i><i>Streptomyces ficellus</i> 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. <a href="https://pubmed.ncbi.nlm.nih.gov/21483943/">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.</a> <br><strong>Products Related to Nojirimycin Bisulfite</strong> <a href="https://moleculardepot.com/product-category/Peptides/">: Peptides</a>