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Tepoxalin

CAS No. 103475-41-8

Tepoxalin ( ORF-20485 | ORF20485 | ORF 20485 | RWJ-20485 | RWJ 20485 | RWJ20485 )

产品货号. M28562 CAS No. 103475-41-8

Tepoxalin 是一种 5-脂氧合酶抑制剂,可用于治疗哮喘、骨关节炎。替泊沙林抑制 COX-1、COX-2 和 5-LOX。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥988 有现货
10MG ¥1442 有现货
25MG ¥3345 有现货
50MG ¥5006 有现货
100MG ¥7120 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Tepoxalin
  • 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
    Tepoxalin 是一种 5-脂氧合酶抑制剂,可用于治疗哮喘、骨关节炎。替泊沙林抑制 COX-1、COX-2 和 5-LOX。
  • 产品描述
    Tepoxalin is a 5-lipoxygenase inhibitor potentially for the treatment of asthma, osteoarthritis. Tepoxalin inhibits COX-1, COX-2, and 5-LOX. Tepoxalin is a potent inhibitor of sheep seminal vesicle cyclooxygenase (COX) (IC50 = 4.6 microM), rat basophilic leukemia cell (RBL-1) lysate COX (IC50 = 2.85 microM) and COX from intact RBL-1 cells (IC50 = 4.2 microM).(In Vitro):Tepoxalin inhibits the production of thromboxane B2 (TxB2) in Ca++ ionophore A-23187-stimulated human peripheral blood leukocytes (HPBL; IC50 = 0.01 microM) and human whole blood (IC50 = 0.08 microM) and is a potent inhibitor of epinephrine-induced human platelet aggregation (IC50 = 0.045 microM). Tepoxalin inhibits lipoxygenase (LOX) in RBL-1 lysates (IC50 = 0.15 microM) and intact RBL-1 cells (IC50 = 1.7 microM) and inhibits the generation of leukotriene B4 (LTB4) in calcium ionophore A-23187-stimulated HPBL (IC50 = 0.07 microM) and human whole blood (IC50 = 1.57 microM). Human platelet 12-LOX (IC50 = 3.0 microM) is inhibited, but 15-LOX is only weakly so (IC50 = 157 microM). (In Vivo):Tepoxalin inhibits inflammation and microvascular dysfunction induced by abdominal irradiation in rats.In vivo, tepoxalin, administered orally, demonstrated potent anti-inflammatory activity in the established adjuvant arthritic rat (ED50 = 3.5 mg/kg) and potent analgesic activity in the acetic acid abdominal construction assay in mice (ED50 = 0.45 mg/kg). In an ex vivo whole blood eicosanoid production assay, tepoxalin produces a dose-related inhibition of prostaglandin (PG) and LT production in dogs (PGF2 alpha - ED50 = 0.015 mg/kg; LTB4 - ED50 = 2.37 mg/kg) and adjuvant arthritic rats following oral administration. In adjuvant arthritic rats, tepoxalin is devoid of ulcerogenic activity within its anti-inflammatory therapeutic range (1-33 mg/kg p.o.) and does not exhibit ulcerogenic activity in normal rats at doses lower than 100 mg/kg (UD50 = 173 mg/kg p.o.).
  • 体外实验
    ——
  • 体内实验
    ——
  • 同义词
    ORF-20485 | ORF20485 | ORF 20485 | RWJ-20485 | RWJ 20485 | RWJ20485
  • 通路
    Immunology/Inflammation
  • 靶点
    Lipoxygenase
  • 受体
    GABAA
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    103475-41-8
  • 分子量
    385.85
  • 分子式
    C20H20ClN3O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 100 mg/mL (259.17 mM)
  • SMILES
    COc1ccc(cc1)-n1nc(CCC(=O)N(C)O)cc1-c1ccc(Cl)cc1
  • 化学全称
    ——

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.N Zheleznova, et al. alpha1beta2delta, a silent GABAA?receptor: recruitment by tracazolate and neurosteroids. Br J Pharmacol. 2008 Mar;153(5):1062-71.
产品手册
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