5-Bromoindole (Highly Pure)

<strong>5-Bromoindole (Highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2016226_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 50 g_x000D_ <strong>Molecular Weight or Concentration:</strong> 196.05 g/mol_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> 2-8°C_x000D_ <strong>Keywords:</strong> 5-Bromoindole 99.5+%_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: Hassan OM, Kubba A, Tahtamouni LH. Novel 5-bromoindole-2-carboxylic Acid Derivatives as EGFR Inhibitors: Synthesis, Docking Study, and Structure Activity Relationship Anticancer Agents Med Chem. 2023;23(11):1336-1348._x000D_ 2: Butler-Fernández KM, Ramos Z, Francis-Malavé AM, Bloom J, Dharmawardhane S, Hernández E. Synthesis, Anti-Cancer and Anti-Migratory Evaluation of 3,6-Dibromocarbazole and 5-Bromoindole Derivatives Molecules. 2019 Jul 24;24(15):2686._x000D_ 3: Tasdemir D, Bugni TS, Mangalindan GC, Concepción GP, Harper MK, Ireland CM. Cytotoxic bromoindole derivatives and terpenes from the Philippine marine sponge Smenospongia sp Z Naturforsch C J Biosci. 2002 Sep-Oct;57(9-10):914-22._x000D_ 4: Tupper J, Stratford MR, Hill S, Tozer GM, Dachs GU. In vivo characterization of horseradish peroxidase with indole-3-acetic acid and 5-bromoindole-3-acetic acid for gene therapy of cancer Cancer Gene Ther. 2010 Jun;17(6):420-8._x000D_ 5: Suárez-Castillo OR, Beiza-Granados L, Meléndez-Rodríguez M, Alvarez-Hernández A, Morales-Ríos MS, Joseph-Nathan P. Synthesis of bromoindole alkaloids from Laurencia brongniartii J Nat Prod. 2006 Nov;69(11):1596-600._x000D_ 6: Bengtsson C, Gravenfors Y. Rapid Construction of a Chloromethyl-Substituted Duocarmycin-like Prodrug Molecules. 2023 Jun 16;28(12):4818._x000D_ 7: Mphahlele MJ, Parbhoo N. Synthesis, Evaluation of Cytotoxicity and Molecular Docking Studies of the 7-Acetamido Substituted 2-Aryl-5-bromo-3-trifluoroacetylindoles as Potential Inhibitors of Tubulin Polymerization Pharmaceuticals (Basel). 2018 Jun 11;11(2):59._x000D_ 8: Médici R, Garaycoechea JI, Dettorre LA, Iribarren AM, Lewkowicz ES. Biocatalysed halogenation of nucleobase analogues Biotechnol Lett. 2011 Oct;33(10):1999-2003._x000D_ 9: Manoharan RK, Raorane CJ, Ishaque F, Ahn YH. Antimicrobial photodynamic inactivation of wastewater microorganisms by halogenated indole derivative capped zinc oxide Environ Res. 2022 Nov;214(Pt 3):113905._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/35685375">10: Padányi R, Farkas B, Tordai H, Kiss B, Grubmüller H, Soya N, Lukács GL, Kellermayer M, Hegedűs T. Nanomechanics combined with HDX reveals allosteric drug binding sites of CFTR NBD1 Comput Struct Biotechnol J. 2022 May 23;20:2587-2599. </a>_x000D_ _x000D_ <strong>Products Related to 5-Bromoindole (Highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>