Indomethacin (sodium hydrate)

CAT:
804-HY-14397A-01
Size:
500 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Indomethacin (sodium hydrate) - image 1

Indomethacin (sodium hydrate)

  • UNSPSC Description:

    Indomethacin (Indometacin) sodium hydrateis a potent, orally active COX1/2 inhibitor with IC50 values of 18 nM and 26 nM for COX-1 and COX-2, respectively. Indomethacin sodium hydrateis has anticancer activity and anti-infective activity. Indomethacin sodium hydrateis can be used for cancer, inflammation and viral infection research[1][2][3].
  • Target Antigen:

    Antibiotic; Bacterial; COX; Influenza Virus
  • Type:

    Reference compound
  • Related Pathways:

    Anti-infection;Immunology/Inflammation
  • Applications:

    COVID-19-immunoregulation
  • Field of Research:

    Cancer; Inflammation/Immunology
  • Assay Protocol:

    https://www.medchemexpress.com/indomethacin-sodium-hydrate.html
  • Solubility:

    DMSO : 12.5 mg/mL (ultrasonic;warming;heat to 60°C)|H2O : 25 mg/mL (ultrasonic)
  • Smiles:

    O=C(O[Na])CC1=C(C)N(C(C2=CC=C(Cl)C=C2)=O)C3=C1C=C(OC)C=C3.O.O.O
  • Molecular Weight:

    433.82
  • References & Citations:

    [1]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.|[2]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.|[3]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.
  • Shipping Conditions:

    Room Temperature
  • Clinical Information:

    Launched
  • CAS Number:

    74252-25-8