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首页> 外文期刊>Current Topics in Medicinal Chemistry >G-Protein Coupled Receptor Antagonists-1: Protease Activated Receptor-1 (PAR-1) Antagonists as Novel Cardiovascular Therapeutic Agents (Hot Topic: Structure and property Approaches in Recent Drug Discovery Guest Editor: Guo Zhu Zheng)
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G-Protein Coupled Receptor Antagonists-1: Protease Activated Receptor-1 (PAR-1) Antagonists as Novel Cardiovascular Therapeutic Agents (Hot Topic: Structure and property Approaches in Recent Drug Discovery Guest Editor: Guo Zhu Zheng)

机译:G蛋白偶联受体拮抗剂1:蛋白酶激活受体1(PAR-1)拮抗剂作为新型心血管治疗药物(热门话题:最近药物发现的结构和性质方法来宾编辑:Guo Zhu Zheng)

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摘要

Inhibition of thrombin receptor (PAR-1) is a promising therapeutic approach for the treatment of various cardiovascular disorders such as unstable angina, acute myocardial infarction, stroke, and restenosis. Since a PAR- 1 antagonist is specific for the cellulalr actions of thrombin, and does not interfere with fibrin generation, it is expected to have less bleeding liability than the currently available treatments. Several peptide and non-peptide PAR-1 antagonists with potent inhibition of platelet aggregation have been reported. Antithrombotic effect of a PAR-1 antibody has been demonstrated in a baboon thrombosis model and the antirestenosis property of a PAR-1 antagonist has been demonstrated in a rat model.
机译:抑制凝血酶受体(PAR-1)是用于治疗各种心血管疾病(例如不稳定的心绞痛,急性心肌梗塞,中风和再狭窄)的一种有前途的治疗方法。由于PAR-1拮抗剂对凝血酶的纤维素作用具有特异性,并且不干扰纤维蛋白的产生,因此与目前可用的治疗方法相比,期望其具有更少的出血倾向。已经报道了几种具有有效抑制血小板聚集作用的肽和非肽PAR-1拮抗剂。在狒狒血栓形成模型中已经证明了PAR-1抗体的抗血栓形成作用,在大鼠模型中已经证明了PAR-1拮抗剂的抗再狭窄特性。

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