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Meloxicam

CAS No. 71125-38-7

Meloxicam ( UH-AC 62XX )

产品货号. M15725 CAS No. 71125-38-7

美洛昔康是一种非甾体类抗炎药 (NSAID),用于缓解关节炎(幼年类风湿性关节炎、骨关节炎和类风湿性关节炎)的症状,如炎症、肿胀、僵硬和关节疼痛。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
50MG ¥201 有现货
100MG ¥262 有现货
500MG ¥642 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥296 有现货

生物学信息

  • 产品名称
    Meloxicam
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    美洛昔康是一种非甾体类抗炎药 (NSAID),用于缓解关节炎(幼年类风湿性关节炎、骨关节炎和类风湿性关节炎)的症状,如炎症、肿胀、僵硬和关节疼痛。
  • 产品描述
    Meloxicam is a nonsteroidal anti-inflammatory drug (NSAID) used to relieve the symptoms of arthritis (juvenile rheumatoid arthritis, osteoarthritis, and rheumatoid arthritis), such as inflammation, swelling, stiffness, and joint pain. However, this medicine does not cure arthritis and will only help you as long as you continue to take it. (In Vitro):Meloxicam (Compound 5) is a non-steroidal antiinflammatory agent, inhibits COX activity, with IC50s of 0.49 μM and 36.6 μM for COX-2 and COX-1, respectively. Meloxicam inhibits COX+ tumor cells, but shows no cytotoxicity on CF41.Mg or MDCK cells at 0.25-25 μg/mL. Furthermore, Meloxicam in combination with doxorubicin, has no synergistic effect on CF41.Mg cells. Meloxicam (0.25 μg/mL) decreases CF41.Mg cell migration and invasion, induces decrease in MMP-2 expression, and increases β-catenin phophorylation in CF41.Mg cells, but does not affect the CF41.Mg cell apoptosis.(In Vivo):Meloxicam (10 mg/kg) alone or in combination with rutin significantly decreases paw liking time on 1st day by 55% and 49% compared with the formalin-treated group, respectively, however the combination reduces time non-significantly on 3rd day in mice. Meloxicam alone or in combination with rutin also decreases relative liver weights, reduces MDA contents, induces liver SOD activities, hampers IL-1β content, and significantly reduces the number of positive caspase-3 immunoreactive cells in mice.
  • 体外实验
    Meloxicam (Compound 5) is a non-steroidal antiinflammatory agent, inhibits COX activity, with IC50s of 0.49 μM and 36.6 μM for COX-2 and COX-1, respectively. Meloxicam inhibits COX+ tumor cells, but shows no cytotoxicity on CF41.Mg or MDCK cells at 0.25-25 μg/mL. Furthermore, Meloxicam in combination with doxorubicin, has no synergistic effect on CF41.Mg cells. Meloxicam (0.25 μg/mL) decreases CF41.Mg cell migration and invasion, induces decrease in MMP-2 expression, and increases β-catenin phophorylation in CF41.Mg cells, but does not affect the CF41.Mg cell apoptosis.
  • 体内实验
    Meloxicam (10 mg/kg) alone or in combination with rutin significantly decreases paw liking time on 1st day by 55% and 49% compared with the formalin-treated group, respectively, however the combination reduces time non-significantly on 3rd day in mice. Meloxicam alone or in combination with rutin also decreases relative liver weights, reduces MDA contents, induces liver SOD activities, hampers IL-1β content, and significantly reduces the number of positive caspase-3 immunoreactive cells in mice.
  • 同义词
    UH-AC 62XX
  • 通路
    Chromatin/Epigenetic
  • 靶点
    COX
  • 受体
    COX
  • 研究领域
    Inflammation/Immunology
  • 适应症
    ——

化学信息

  • CAS Number
    71125-38-7
  • 分子量
    351.4
  • 分子式
    C14H13N3O4S2
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: 30 mg/mL (85.37 mM)
  • SMILES
    CC1=CN=C(S1)NC(=O)C2=C(C3=CC=CC=C3S(=O)(=O)N2C)O
  • 化学全称
    (E)-3-(hydroxy((5-methylthiazol-2-yl)amino)methylene)-2-methyl-2H-benzo[e][1,2]thiazin-4(3H)-one 1,1-dioxide

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Poulsen Nautrup B, et al. Dtsch Tierarztl Wochenschr. 1999 Mar;106(3):94-100.
产品手册
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