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首页> 外文期刊>Japanese Journal of Pharmacology >Studies on Alkyl-Xanthine Derivatives II. Pharmacokinetic and Pharmacodynamic Studies of a New Bronchodilator, 1-Methyl-3-Propylxanthine (MPX)
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Studies on Alkyl-Xanthine Derivatives II. Pharmacokinetic and Pharmacodynamic Studies of a New Bronchodilator, 1-Methyl-3-Propylxanthine (MPX)

机译:烷基黄嘌呤衍生物的研究II。新型支气管扩张药1-甲基-3-丙基黄嘌呤(MPX)的药代动力学和药效学研究

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摘要

References(17) Cited-By(12) A new xanthine derivative bronchodilator, 1-methyl-3-propylxanthine (MPX), and 1-methyl-3-butylxanthine (MBX) were synthesized. We evaluated their relaxant effects on tracheal smooth muscle isolated from guinea pigs and pharmacokinetic characteristics in rats using 1, 3-dimethylxanthine (theophylline, TPH) as the reference drug. Dose-dependent relaxant effects were observed in the concentration range of 1 × 10-6 to 1 × 10-4 M, and both MPX and MBX exert very much stronger relaxant effects than TPH with nearly equal potency. There were significant differences in the pharmacokinetic and physico-chemical properties among these drugs, both MPX and MBX having shorter half-lives, higher plasma protein binding in vivo and stronger hydrophobicity compared to TPH. The present study suggested that the N3-alkyl chain length is significant for increasing the relaxant effect and affecting the pharmacokinetic and physico-chemical properties of these drugs.
机译:参考文献(17)引用了(12)合成了一种新的黄嘌呤衍生物支气管扩张剂1-甲基-3-丙基黄嘌呤(MPX)和1-甲基-3-丁基黄嘌呤(MBX)。我们使用1,3-二甲基黄嘌呤(茶碱,TPH)作为参考药物评估了它们对豚鼠气管平滑肌的松弛作用以及大鼠的药代动力学特征。在1×10-6至1×10-4 M的浓度范围内观察到了剂量依赖性的松弛作用,并且MPX和MBX都比TPH发挥了非常强的松弛作用,并且具有几乎相等的效力。这些药物的药代动力学和理化性质存在显着差异,与TPH相比,MPX和MBX的半衰期更短,体内血浆蛋白结合更高,疏水性更强。本研究表明,N3-烷基链长对于增加松弛作用并影响这些药物的药代动力学和理化性质具有重要意义。

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