首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Studies on some para-substituted clonidine derivatives that exhibit an alpha-adrenoceptor stimulant activity.
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Studies on some para-substituted clonidine derivatives that exhibit an alpha-adrenoceptor stimulant activity.

机译:对某些具有α-肾上腺素受体刺激活性的对位可乐定衍生物的研究。

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摘要

1 alpha-Adrenoceptor stimulant activity was determined for noradrenaline (NA), clonidine and a series of para-substituted derivatives of clonidine on rat aortic strips, a rat brain synaptosome preparation, and anaesthetized pithed rats. The effects on the blood pressure of intraventricular (i.c.v.) injections of para-aminoclonidine were also determined in anaesthetized rats. 2 Para-substituted derivatives of clonidine (amino-, diethylamino-, ethylamino-, acetamido-, bromoacetamido-, N-chloroethyl-N-methyl-amino and N-beta-chloroethyl-N-methylaminomethyl-) retain alpha-adrenoceptor stimulant activity. 3 pD2 values determined on rat aortic strips were 11.2, 7.67 and 9.05 respectively for para-aminoclonidine, clonidine and noradrenaline. The Ki values of these agents, determined on a rat brain synaptosomal preparation with a radioreceptor assay using [3H]-clonidine as ligand, were 1.3, 8.0 and 23 nM respectively for para-aminoclonidine, clonidine and NA. When given by i.c.v. injection in rats, para-aminoclonidine lowered the blood pressure. 4 N-beta-chloroethyl-N-methylaminomethylclonidine is an alkylating agent with an unusual agonist activity. It elicits contractions of the rat aorta that persist despite repeated washing. 5 alpha-Adrenoceptor affinities are discussed in relation to their structural features.
机译:测定了去甲肾上腺素(NA),可乐定和大鼠主动脉条上的可乐定的一系列对位取代衍生物,大鼠脑突触制剂和麻醉的成年大白鼠的1α-肾上腺素能受体兴奋活性。还在麻醉的大鼠中确定了对室内注射对氨基可乐定对血压的影响。 2可乐定的对位取代衍生物(氨基,二乙氨基,乙氨基,乙酰胺基,溴乙酰胺基,N-氯乙基-N-甲基氨基和N-β-氯乙基-N-甲基氨基甲基-)保留α-肾上腺素受体刺激活性。对主氨基可乐定,可乐定和去甲肾上腺素在大鼠主动脉条上测定的3 pD2值分别为11.2、7.67和9.05。在对端氨基可乐定,可乐定和NA的大鼠脑突触体制剂中,使用[3H]-可乐定作为配体,通过放射性受体测定,确定这些试剂的Ki值分别为1.3、8.0和23 nM。由i.c.v.在大鼠中注射对氨基可乐定可降低血压。 4N-β-氯乙基-N-甲基氨基甲基可乐定是一种具有异常激动剂活性的烷基化剂。尽管反复洗涤,它仍会引起大鼠主动脉收缩。关于它们的结构特征,讨论了5种α-肾上腺素受体亲和力。

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