首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Antiarrhythmic, serotonin antagonist and antianxiety activities of novel substituted thiophene derivatives synthesized from 2-amino-4,5,6,7-tetrahydro-N-phenylbenzo(b)thiophene-3-carboxamide.
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Antiarrhythmic, serotonin antagonist and antianxiety activities of novel substituted thiophene derivatives synthesized from 2-amino-4,5,6,7-tetrahydro-N-phenylbenzo(b)thiophene-3-carboxamide.

机译:由2-氨基-4,5,6,7-四氢-N-苯基苯并(b)噻吩-3-羧酰胺合成的新型取代噻吩衍生物的抗心律不齐,血清素拮抗剂和抗焦虑活性。

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摘要

A series of novel thiophene derivatives 3-17 were synthesized by initial reactions of 2-amino-4,5,6,7-tetrahydro-N-phenylbenzo[b]thiophene-3-carboxamide 1 and 2-amino-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carbonitrile 7 with different organic reagents. The structures of newly synthesized compounds were confirmed by IR, 1H NMR, MS spectral data and elemental analysis. Initially the acute toxicity of the compounds was assayed via the determination of their LD50. All the compounds were screened for their antiarrhythmic, serotonin antagonist and antianexiety activities and they showed high activity compared with procaine amide, lidocaine, diazepam and buspirone as positive controls. The detailed synthesis, spectroscopic data, LD50 and pharmacological activities of the synthesized compounds were reported.
机译:通过2-氨基-4,5,6,7-四氢-N-苯基苯并[b]噻吩-3-羧酰胺1和2-氨基-4,5的初始反应合成了一系列新型的噻吩衍生物3-17, 6,7-四氢苯并[b]噻吩-3-腈7与不同的有机试剂。通过IR,1 H NMR,MS光谱数据和元素分析确认了新合成的化合物的结构。最初,通过确定其LD50来测定化合物的急性毒性。筛选了所有化合物的抗心律失常,5-羟色胺拮抗剂和抗焦虑活性,与普鲁卡因酰胺,利多卡因,地西pi和丁螺环酮作为阳性对照相比,它们显示出高活性。报道了合成化合物的详细合成,光谱数据,LD50和药理活性。

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