5-Bromoindole-2-carboxylic Acid (Highly Pure)

<strong>5-Bromoindole-2-carboxylic Acid (Highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2016305_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 5 g_x000D_ <strong>Molecular Weight or Concentration:</strong> 240.06 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> 5-Bromoindole-2-carboxylic acid_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: Jahangir S, Eglin D, Pötter N, Khozaei Ravari M, Stoddart MJ, Samadikuchaksaraei A, Alini M, Baghaban Eslaminejad M, Safa M. Inhibition of hypertrophy and improving chondrocyte differentiation by MMP-13 inhibitor small molecule encapsulated in alginate-chondroitin sulfate-platelet lysate hydrogel Stem Cell Res Ther. 2020 Oct 9;11(1):436._x000D_ 3: 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_ 4: Jahangir S, Eglin D, Pötter N, Khozaei Ravari M, Stoddart MJ, Samadikuchaksaraei A, Alini M, Baghaban Eslaminejad M, Safa M. Inhibition of hypertrophy and improving chondrocyte differentiation by MMP-13 inhibitor small molecule encapsulated in alginate-chondroitin sulfate-platelet lysate hydrogel Stem Cell Res Ther. 2020 Oct 9;11(1):436._x000D_ 5: Khan M. The antischistosomal activity of substituted indoles J Environ Sci Health B. 1983 Dec;18(6):781-93._x000D_ 6: Manoso AS, Ahn C, Soheili A, Handy CJ, Correia R, Seganish WM, Deshong P. Improved synthesis of aryltrialkoxysilanes via treatment of aryl Grignard or lithium reagents with tetraalkyl orthosilicates J Org Chem. 2004 Nov 26;69(24):8305-14._x000D_ 7: Meyer A, Würsten M, Schmid A, Kohler HP, Witholt B. Hydroxylation of indole by laboratory-evolved 2-hydroxybiphenyl 3-monooxygenase J Biol Chem. 2002 Sep 13;277(37):34161-7._x000D_ 8: Yan X, Tang XX, Qin D, Yi ZW, Fang MJ, Wu Z, Qiu YK. Biosynthetic Functional Gene Analysis of Bis-Indole Metabolites from 25D7, a Clone Derived from a Deep-Sea Sediment Metagenomic Library Mar Drugs. 2016 Jun 1;14(6):107._x000D_ 9: Munir IZ, Dordick JS. Soybean peroxidase as an effective bromination catalyst* Enzyme Microb Technol. 2000 Mar 1;26(5-6):337-341._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/29170897">10: Carey LM, Kim KB, McCombs NL, Swartz P, Kim C, Ghiladi RA. Selective tuning of activity in a multifunctional enzyme as revealed in the F21W mutant of dehaloperoxidase B from Amphitrite ornata J Biol Inorg Chem. 2018 Mar;23(2):209-219. </a>_x000D_ _x000D_ <strong>Products Related to 5-Bromoindole-2-carboxylic Acid (Highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>