202409-33-4/Etoricoxib

Quick Details
Molecular Formula:C18H15ClN2O2S
Molecular Weight:358.848
Appearance:off-white powder
CasNo:202409-33-4

  • Product Details

    Etoricoxib Good Manufacturer supply High Quality 202409-33-4

    • Molecular Formula:C18H15ClN2O2S
    • Molecular Weight:358.848
    • Appearance/Colour:off-white powder 
    • Vapor Pressure:5.17E-10mmHg at 25°C 
    • Melting Point:134-135 °C 
    • Refractive Index:1.6 
    • Boiling Point:510 °C at 760 mmHg 
    • PKA:4.5(at 25℃) 
    • Flash Point:262.2 °C 
    • PSA:68.30000 
    • Density:1.298 g/cm3 
    • LogP:5.25670 

    Etoricoxib (202409-33-4) Usage

    Etoricoxib is a COX-2 inhibitor developed as a follow-up of rofecoxib for the treatment of osteoarthritis, rheumatoid arthritis, dysmenorrhoea, gout, ankylosing spondylitis and pain. Several processes describe the preparation of etoricoxib in 4 or 5 steps from 6- methylnicotinate. The key step is the novel pyridine construction using annulation of a ketosutfone with a vinamidinium synthon. In human whole blood, in vitro, the IC50 value obtained for inhibition of COX-2 is 1 .I μM as compared to 116 μM obtained for inhibition of COX-1. Thus, etoricoxib is the most selective COX-2 inhibitor to date, with a COX-IKOX- 2 ratio of IC50 values of 106 for etoricoxib as compared to 35, 30, 7.6 for rofecoxib, valdecoxib and celecoxib, respectively. Its in vivo potency is generally comparable to that of rofecoxib in animal models against inflammation (carrageenan-induced paw edema), pyrexia (LPS-induced pyresis), pain (carrageenan-induced hyperalgesia) and arthritis (adjuvant-induced arthritis). Etoricoxib is well tolerated with dose-proportional pharmacokinetics. It has no effect on bleeding time or platelet ag regation. The gastrointestinal tolerability of etoricoxib is excellent as demonstrated by [51Cr] models of excretion in rats and squirrel monkeys. Moreover, etoricoxib, unlike naproxen is not associated with significant inhibition of gastric mucosal PGE2 synthesis compared to placebo. Etoricoxib is highly absorbed, has a tmax of 1.5 h and a half-life time of approximately 15-22h. Five metabolites, weak inhibitors of COX-1 and COX-2 have been identified after renal excretion. Finally, although multiple CYP enzymes are involved in the metabolism of etoricoxib (CYP3A4 being the major contributor), etoricoxib is not a potent CYP3A4 inhibitor or inducer. In patients undergoing molar extraction, etoricoxib showed similar efficacy to naproxen sodium with a longer duration of analgesia than acetaminophen/codeine (approximately >24 h, 22 h and 5.2 h, respectively) and a better total pain relief score over 8 h. Similar efficacy of etoricoxib and naproxen was also seen in patients suffering of osteoarthritis. In the treatment of rheumatoid arthritis and ankylosing spondylitis, etoricoxib demonstrated significantly superior efficacy compared to naproxen and placebo. Etoricoxib did not affect the pharmacokinetics of prednisolone (i.v. or p.0.) and its co-administration with antacids showed insignificant effects on the maximal concentration and its absorption. .

    How to get the best price on Etoricoxib?

    Zibo Hangyu Biotechnology Development Co., Ltd is a quality supplier and manufacturer of Etoricoxib . You can buy high quality, low price Etoricoxib 202409-33-4 here.

    Zibo Hangyu Biotechnology Development Co., Ltd. is a comprehensive chemical enterprise focusing on fine chemical products and pharmaceutical intermediates, integrating research and development, production and sales. The company is equipped with advanced equipment quality inspection and research center. At the same time, the company has excellent talents with rich experience in process development and quality control. To provide customers with total solutions from raw material processing to chemical synthesis systems. The company has established a standardized and perfect quality standard system to provide stable and high quality production and service.

    Milestones

    • 2012yearThe company was founded, began to engage in the production and supply of chemical raw materials
    • 2014yearExpand the scale of production, pharmaceutical raw materials production workshop was established
    • 2016yearCooperated with domestic and foreign chemical platforms to promote self-produced and high-end pharmaceutical intermediates
    • 2019yearIn recent years to participate in the international pharmaceutical raw materials exhibitions
    • 2023yearBusiness continues to expand, Production and Sales teams continue to grow
    • 2026yearPlans to set up foreign branches


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