5-Methoxy-2-methylindole (Highly Pure)

<strong>5-Methoxy-2-methylindole (Highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2016304_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 250 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 161.21 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-Methoxy-2-methylindole_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: Indomethacin 2021 Jan 18. Drugs and Lactation Database (LactMed®) [Internet]. Bethesda (MD): National Institute of Child Health and Human Development; 2006–._x000D_ 2: Tanaka I, Yoshizumi H, Tanaka Y, Takeda S, Kamei C, Nakaya N, Kitazumi K, Tagami H, Tasaka K. Pharmacological profiles of 2-carboxyphenyl-1-(4-chlorobenzoyl)-5-methoxy-2-methylindole-3-acetate and 2-[(2-carboxyphenoxy)-carbonyl]phenyl-1-(4-chlorobenzoyl)-5-meth oxy-2- methylindole-3-acetate, new antiinflammatory agents Arzneimittelforschung. 1986 Apr;36(4):703-9._x000D_ 3: WINTER CA, RISLEY EA, NUSS GW. ANTI-INFLAMMATORY AND ANTIPYRETIC ACTIVITIES OF INDOMETHACIN, 1-(P-CHLOROBENZOYL)-5-METHOXY-2-METHYLINDOLE-3-ACETIC ACID J Pharmacol Exp Ther. 1963 Sep;141:369-76._x000D_ 4: Paris GY, Garmaise DL, Cimon DG, Swett L, Carter GW, Young P. Glycerides as prodrugs. 3. Synthesis and antiinflammatory activity of [1-(p-chlorobenzoyl)-5-methoxy-2-methylindole-3-acetyl]glycerides (indomethacin glycerides) J Med Chem. 1980 Jan;23(1):9-13._x000D_ 5: O'Hara E, Seymour J. Inducing metamorphosis in the irukandji jellyfish Carukia barnesi Sci Rep. 2022 May 31;12(1):9052._x000D_ 6: Giordano M, Capelli L, Chianese U. The therapeutic activity of 1-(p-chlorobenzoyl)-5-methoxy-2-methylindole-3-acetic acid monohydrate glucosamide in rheumatoid arthritis (double blind trial) Arzneimittelforschung. 1975 Mar;25(3):435-7._x000D_ 7: Ueda I, Ishii K, Arai H, Ikeda S, Hitomi Y, Hatanaka M. Design, synthesis and antiinflammatory activity of a new indomethacin ester. 2-[N-[3-(3-(piperidinomethyl)phenoxy)propyl]carbamoylmethylthio]ethyl 1-(p-chlorobenzoyl)-5-methoxy-2-methyl-indole-3-acetate Chem Pharm Bull (Tokyo). 1991 Mar;39(3):679-84._x000D_ 8: Helleberg L. Clinical Pharmacokinetics of indomethacin Clin Pharmacokinet. 1981 Jul-Aug;6(4):245-58._x000D_ 9: Kistenmacher TJ, Marsh RE. Crystal and molecular structure of an antiinflammatory agent, indomethacin, 1-(p-chlorobenzoyl)-5-methoxy-2-methylindole-3-acetic acid J Am Chem Soc. 1972 Feb 23;94(4):1340-5._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/29281657">10: Helm RR, Dunn CW. Indoles induce metamorphosis in a broad diversity of jellyfish, but not in a crown jelly (Coronatae) PLoS One. 2017 Dec 27;12(12):e0188601. </a>_x000D_ _x000D_ <strong>Products Related to 5-Methoxy-2-methylindole (Highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>