Suppr超能文献

1-(3-苄氧基-1[E]辛烯基)咪唑对血小板血栓素合成酶的抑制作用

Inhibition of platelet thromboxane synthetase by 1-(3-benzyloxy-1[E]octenyl)imidazole.

作者信息

Sincholle D, Coquelet C, Bonne C

出版信息

Arzneimittelforschung. 1986;36(1):117-9.

PMID:3082339
Abstract

1-(3-Benzyloxy-1[E]octenyl)imidazole (CBS-645) is a specific inhibitor of thromboxane synthetase. It inhibits the platelet enzyme in human and rabbit at micromolar concentrations. At a dose of 12.5 mg kg-1 in rabbits, CBS-645 displays a prolonged inhibitory effect on the formation of thromboxane (Tx) B2 induced by blood coagulation in vitro. In human volunteers, an oral dose of 50 mg leads to an average 70% inhibition of TxB2 formation. CBS-645 administered at a dose of 25 mg kg-1 p.o. in the rat, significantly increases bleeding time. In another test in which platelet interaction with the vessel wall is involved, i.e. in vivo platelet deposition onto desendothelialized aorta in the rabbit, the drug shows antithrombotic activity after a single oral administration of 5 mg kg-1. CBS-645 could be of interest in the treatment of the various diseases in which the pathological role of thromboxane A2 is suspected.

摘要

1-(3-苄氧基-1[E]辛烯基)咪唑(CBS-645)是血栓素合成酶的特异性抑制剂。它在微摩尔浓度下就能抑制人和兔体内的血小板酶。在兔体内以12.5毫克/千克的剂量给药时,CBS-645对体外血液凝固诱导的血栓素(Tx)B2形成具有持久的抑制作用。在人类志愿者中,口服50毫克的剂量平均会导致TxB2形成受到70%的抑制。在大鼠中以25毫克/千克的口服剂量给药时,CBS-645会显著延长出血时间。在另一项涉及血小板与血管壁相互作用的试验中,即在兔体内血小板在内皮剥脱的主动脉上的沉积试验中,单次口服5毫克/千克的药物后,该药物显示出抗血栓活性。CBS-645可能对治疗各种怀疑血栓素A2具有病理作用的疾病有意义。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验