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

Product Description 5/5 - (2 votes) 5-Bromoindole-2-carboxylic Acid (Highly Pure) Catalog number: B2016305 Lot number: Batch Dependent Expiration Date: Batch dependent Amount: 5 g Molecular Weight or Concentration: 240.06 g/mol Supplied as: Powder Applications: a molecular tool for various biochemical applications Storage: -20°C Keywords: 5-Bromoindole-2-carboxylic 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. References: 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. 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. 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. 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. 5: Khan M. The antischistosomal activity of substituted indoles J Environ Sci Health B. 1983 Dec;18(6):781-93. 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. 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. 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. 9: Munir IZ, Dordick JS. Soybean peroxidase as an effective bromination catalyst* Enzyme Microb Technol. 2000 Mar 1;26(5-6):337-341. 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. Products Related to 5-Bromoindole-2-carboxylic Acid (Highly Pure) can be found at Chemicals