Indomethacin-13C6

Indomethacin-13C6 (Indometacin-13C6) is 13C labeled Indomethacin. Indomethacin (Indometacin) is a potent, orally active COX1/2 inhibitor with IC50 values of 18 nM and 26 nM for COX-1 and COX-2, respectively. Indomethacin has anticancer activity and anti-infective activity. Indomethacin can be used for cancer, inflammation and viral infection research[1][2][3].

Product Specifications

Product Name Alternative

Indometacin-13C6

UNSPSC

12352005

Target

Antibiotic; Bacterial; COX; Influenza Virus; Isotope-Labeled Compounds

Related Pathways

Anti-infection; Immunology/Inflammation; Others

Applications

COVID-19-anti-virus

Field of Research

Cancer; Inflammation/Immunology

Smiles

COC1=CC=C(C2=C1)N(C(C)=C2CC(O)=O)C([13C]3=[13CH][13CH]=[13C]([13CH]=[13CH]3)Cl)=O

Molecular Formula

C13 13C6H16ClNO4

Molecular Weight

363.74

References & Citations

[1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53 (2) :211-216.|[2]Helleberg L, et, al. Clinical Pharmacokinetics of indomethacin. Clin Pharmacokinet. 1981 Jul-Aug;6 (4) :245-58.|[3]Sabiu S, et, al. Indomethacin-induced gastric ulceration in rats: Protective roles of Spondias mombin a nd Ficus exasperate. Toxicol Rep. 2015 Jan 8:2:261-267.|[4]Danisman B, et, al, Carnosic Acid Ameliorates Indomethacin-Induced Gastric Ulceration in Rats by Alleviating Oxidative Stress and Inflammation. Biomedicines. 2023 Mar 9;11 (3) :829.|[5]Riendeau D, et, al. Biochemical and pharmacological profile of a tetrasubstituted furanone as a highly selective COX-2 inhibitor. Br J Pharmacol. 1997 May;121 (1) :105-17.|[6]Eli Y, et, al. Comparative effects of indomethacin on cell proliferation and cell cycle progression in tumor cells grown in vitro and in vivo. Biochem Pharmacol. 2001 Mar 1;61 (5) :565-71.|[7]Amici C, et, al. Inhibition of viral protein translation by indomethacin in vesicular stomatitis virus infection: role of eIF2α kinase PKR. Cell Microbiol. 2015 Sep;17 (9) :1391-404.