人受体p2y12复合物与r-138727分子的分子模拟

A. Morozova, A. Bakunovich
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引用次数: 0

摘要

各种局部动脉粥样硬化血栓形成是全世界人类死亡的主要原因。对抗这种病理的关键是指定抗血小板药物。这些药物在抑制血小板活性的机制上各不相同。Prasugrel是噻吩吡啶类拮抗剂,是P2Y12类血小板ADP受体介导的血小板活化和聚集的有效抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MOLECULAR MODELING OF THE P2Y12 COMPLEX OF HUMAN RECEPTOR WITH R-138727 MOLECULE
The leading cause of human death throughout the world is atherothrombosis of various localization. The key point in the fight against this pathology is the appointment of antiplatelet agents. These drugs differ from each other in the mechanism of inhibiting platelet activity. Prasugrel, an antagonist of the thienopyridine class, is a potent inhibitor of platelet activation and aggregation mediated by platelet ADP receptors of the P2Y12 class.
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