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一系列与1H-吲哚-3-羧酸内型8-甲基-8-氮杂双环[3.2.1]辛-3-基酯化学相关的芳基托烷酯和酰胺的合成及生物活性。一种具有强效抗伤害感受活性的5-HT4激动剂的研发。

Synthesis and biological activity of a series of aryl tropanyl esters and amides chemically related to 1H-indole-3-carboxylic acid endo 8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester. Development of a 5-HT4 agonist endowed with potent antinociceptive activity.

作者信息

Romanelli M N, Ghelardini C, Dei S, Matucci R, Mori F, Scapecchi S, Teodori E, Bartolini A, Galli A, Giotti A

出版信息

Arzneimittelforschung. 1993 Aug;43(8):913-8.

PMID:8216452
Abstract

A series of aryl tropanyl esters and amides related to 1H-indole-3-carboxylic acid endo 8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester (ICS 205930, CAS 89565-68-4) were synthesized and evaluated for antinociceptive activity using the hot-plate test. Of these, the benzofurane-3-carboxylic ester of tropine (1) was found powerfully to increase the pain threshold, with a cholinergic mechanism of action. Despite the structural similarity with ICS 205930, the analgesia induced by 1 seems not to be due to 5-HT3 receptor interaction, and there is evidence of involvement of the central 5-HT4 receptor.

摘要

合成了一系列与1H-吲哚-3-羧酸内型8-甲基-8-氮杂双环[3.2.1]辛-3-基酯(ICS 205930,CAS 89565-68-4)相关的芳基托烷酯和酰胺,并使用热板试验评估了它们的抗伤害感受活性。其中,发现托品的苯并呋喃-3-羧酸酯(1)能显著提高痛阈,其作用机制为胆碱能机制。尽管与ICS 205930结构相似,但1诱导的镇痛作用似乎不是由于5-HT3受体相互作用,且有证据表明中枢5-HT4受体参与其中。

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