8-hydroxyquinoline-β-D-galactopyranoside (8-hydroxy-1-azanaphthalene-β-D-galactoside)

<strong>8-hydroxyquinoline-β-D-galactopyranoside (8-hydroxy-1-azanaphthalene-β-D-galactoside)</strong>_x000D_ <strong>Catalog number:</strong> B2015715_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 200 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 307.30 g/mol_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20 °C_x000D_ <strong>Keywords:</strong> 8-Hydroxy-1-azanaphthalene-β-D-galactoside_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: da Silva NM, Gentz CB, Reginatto P, Fernandes THM, Kaminski TFA, Lopes W, Quatrin PM, Vainstein MH, Abegg MA, Lopes MS, Fuentefria AM, de Andrade SF. 8-Hydroxyquinoline 1,2,3-triazole derivatives with promising and selective antifungal activity Med Mycol. 2021 May 4;59(5):431-440._x000D_ 2: Joaquim AR, Gionbelli MP, Gosmann G, Fuentefria AM, Lopes MS, Fernandes de Andrade S. Novel Antimicrobial 8-Hydroxyquinoline-Based Agents: Current Development, Structure-Activity Relationships, and Perspectives J Med Chem. 2021 Nov 25;64(22):16349-16379._x000D_ 3: Reginatto P, Joaquim AR, Rocha DA, Berlitz SJ, Külkamp-Guerreiro IC, De Andrade SF, Fuentefria AM. 8-hydroxyquinoline and quinazoline derivatives as potential new alternatives to combat Candida spp. biofilm Lett Appl Microbiol. 2022 Mar;74(3):395-404._x000D_ 4: Ma X, Lu J, Yang P, Zhang Z, Huang B, Li R, Ye R. 8-Hydroxyquinoline-modified ruthenium(II) polypyridyl complexes for JMJD inhibition and photodynamic antitumor therapy Dalton Trans. 2022 Sep 20;51(36):13902-13909._x000D_ 5: Pippi B, Joaquim AR, Lopes W, Machado GRM, Bergamo VZ, Giuliani LM, Abegg MA, Cruz L, Vainstein MH, Fuentefria AM, de Andrade SF. 8-Hydroxyquinoline-5-sulfonamides are promising antifungal candidates for the topical treatment of dermatomycosis J Appl Microbiol. 2020 Apr;128(4):1038-1049._x000D_ 6: Marquez-Gomez PL, Kruyer NS, Eisen SL, Torp LR, Howie RL, Jones EV, France S, Peralta-Yahya P. Discovery of 8-Hydroxyquinoline as a Histamine Receptor 2 Blocker Scaffold ACS Synth Biol. 2022 Aug 19;11(8):2820-2828._x000D_ 7: Seo H, Jackl MK, Kalaj M, Cohen SM. Developing Metal-Binding Isosteres of 8-Hydroxyquinoline as Metalloenzyme Inhibitor Scaffolds Inorg Chem. 2022 May 16;61(19):7631-7641._x000D_ 8: Ma L, Xuan X, Fan M, Zhang Y, Yuan G, Huang G, Liu Z. A novel 8-hydroxyquinoline derivative induces breast cancer cell death through paraptosis and apoptosis Apoptosis. 2022 Aug;27(7-8):577-589._x000D_ 9: Kotian A, Kamat V, Naik K, Kokare DG, Kumara K, Neratur KL, Kumbar V, Bhat K, Revankar VK. 8-Hydroxyquinoline derived p-halo N4-phenyl substituted thiosemicarbazones: Crystal structures, spectral characterization and in vitro cytotoxic studies of their Co(III), Ni(II) and Cu(II) complexes Bioorg Chem. 2021 Jul;112:104962._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/33513476">10: Gupta R, Luxami V, Paul K. Insights of 8-hydroxyquinolines: A novel target in medicinal chemistry Bioorg Chem. 2021 Mar;108:104633. </a>_x000D_ _x000D_ <strong>Products Related to 8-hydroxyquinoline-β-D-galactopyranoside (8-hydroxy-1-azanaphthalene-β-D-galactoside) can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>