5-Bromoindole-2-carboxylic Acid (Highly Pure)
Original price was: $1,395.00.$695.00Current price is: $695.00.
Catalog Number: B2016305 (5 g)
5-Bromoindole-2-carboxylic Acid (Highly Pure) is a high quality heterocyclic building block used to synthesize a variety of biochemical compounds. This product has been used as a molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.
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In stock
Product Description
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
Additional Information
| Weight | 0.8 oz |
|---|---|
| Dimensions | 2 × 0.9 × 0.9 in |
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