首页> 外文期刊>European Journal of Pharmacology: An International Journal >A new pyrazolo pyrimidine derivative inhibitor of cyclooxygenase-2 with anti-angiogenic activity.
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A new pyrazolo pyrimidine derivative inhibitor of cyclooxygenase-2 with anti-angiogenic activity.

机译:一种新型的具有抗血管生成活性的环加氧酶-2的吡唑并嘧啶衍生物抑制剂。

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摘要

In a previous study, we reported a new pyrazolo pyrimidine derivative, N(4)-benzyl-N(6),N(6)-dimethyl-1-1(tert-butyl)-1H-pyrazolo[3,4-d]pyrimidin e-6,4-diamine (DPP), which inhibited potently cyclooxygenase-2 activity in intact cell assays with minor activity against cyclooxygenase-1 (IC(50)=0.9 nM for cyclooxygenase-2 versus IC(50)=59.6 nM for cyclooxygenase-1). In the present work, this behaviour was confirmed in vivo by using the 24-h zymosan-injected mouse air pouch model (ID(50)=1.36 nM/pouch for prostaglandin E(2) level). We also studied the possible beneficial effect of DPP in the angiogenesis-dependent murine air pouch granuloma and rat paw carrageenan-induced hyperalgesia models. DPP exerted analgesic and anti-angiogenic (52% reduction in angiogenesis at 10 mg/kg, i.p.) effects that may be associated with inhibition of cyclooxygenase-2 activity.
机译:在以前的研究中,我们报道了一种新的吡唑并嘧啶衍生物,N(4)-苄基-N(6),N(6)-二甲基-1-1(叔丁基)-1H-吡唑并[3,4-d ] pyrimidin e-6,4-diamine(DPP),在完整细胞测定中可有效抑制环氧合酶2的活性,而对环氧合酶1的活性较小(环氧合酶2的IC(50)= 0.9 nM,而IC(50)= 59.6 nM为环氧合酶-1)。在目前的工作中,通过使用24小时注入酵母聚糖的小鼠空气囊模型(ID(50)= 1.36 nM /囊,前列腺素E(2)水平)在体内证实了这种行为。我们还研究了DPP在依赖血管新生的鼠气袋肉芽肿和大鼠爪角叉菜胶诱导的痛觉过敏模型中的可能有益作用。 DPP发挥镇痛和抗血管生成作用(在10 mg / kg腹腔注射时,血管生成减少52%),这可能与环氧合酶2活性的抑制有关。

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