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腺苷5'-三磷酸对豚鼠盲肠离体绦虫抑制作用的拮抗作用:一系列异吲哚酮衍生物的构效关系

Anatagonism of the inhibitory effects of adenosine 5'-triphosphate on the isolated taenia of the guinea-pig caecum: structure-activity relationships within a series of isatogen derivatives.

作者信息

Foster H E, Hooper M, Spedding M, Sweetman A J, Weetman D F

出版信息

Br J Pharmacol. 1978 Jun;63(2):309-14. doi: 10.1111/j.1476-5381.1978.tb09762.x.

Abstract

1 A series of eight isatogen derivatives was studied on isolated tissues taken from guinea-pigs. The ability of the compounds to relax the taenia, to inhibit adenosine 5'-diphosphate (ADP)-stimulated respiration in mitochondria and to antagonize the inhibitory effects of adenosine 5'-triphosphate (ATP) on smooth muscle was measured. 2 All the derivatives inhibited ADP-stimulated respiration in mitochondria and relaxed the smooth muscle. These two effects were found to be significantly correlated. 3 Only half the compounds blocked the inhibitory effects of ATP, and all of these had a chemically reactive group (nitro, methoxy or pyridyl) in the 2'2-position. 2-2'-Pyridylisatogen was the most effective blocking agent. 4 The blockade of the inhibitory effects of ATP is not related to the other actions of the derivatives.

摘要
  1. 对从豚鼠身上获取的离体组织研究了一系列8种异吲哚酮衍生物。测定了这些化合物舒张豚鼠结肠带、抑制线粒体中腺苷5'-二磷酸(ADP)刺激的呼吸作用以及拮抗腺苷5'-三磷酸(ATP)对平滑肌抑制作用的能力。

  2. 所有衍生物均抑制线粒体中ADP刺激的呼吸作用并使平滑肌舒张。发现这两种作用显著相关。

  3. 只有一半的化合物阻断ATP的抑制作用,并且所有这些化合物在2'2-位都有一个化学反应基团(硝基、甲氧基或吡啶基)。2-2'-吡啶基异吲哚酮是最有效的阻断剂。

  4. ATP抑制作用的阻断与衍生物的其他作用无关。

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Studies on prostaglandin antagonists.前列腺素拮抗剂的研究。
Br J Pharmacol. 1971 Aug;42(4):584-94. doi: 10.1111/j.1476-5381.1971.tb07142.x.

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