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AZD6140.

机译:ΑZΔ6140。

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摘要

Oral antiplatelet therapy with P2Y(12) receptor blockers (especially clopidogrel) is the current choice of treatment during acute coronary syndromes and percutaneous interventions. To address the various limitations of thienopyridine therapy (including response variability and non-responsiveness) a novel drug, AZD6140, is under clinical development. AZD6140 is an oral and reversible P2Y(12) receptor blocker that does not require hepatic conversion to an active metabolite and produces an overall superior ADP-induced platelet inhibition with less response variability than clopidogrel. It has fast onset and offset actions that may be advantageous in patients who may have to undergo immediate surgery.
机译:P2Y(12)受体阻滞剂(尤其是氯吡格雷)的口服抗血小板治疗是急性冠状动脉综合征和经皮介入治疗的当前选择。为了解决噻吩并吡啶疗法的各种局限性(包括应答变异性和非应答性),正在开发一种新药AZD6140。 AZD6140是一种口服和可逆的P2Y(12)受体阻滞剂,它不需要肝脏转化为活性代谢物,就产生了总体上优于ADP诱导的血小板抑制作用,并且其反应变异性低于氯吡格雷。它具有快速的起效和抵消作用,这对于可能需要立即进行手术的患者可能是有利的。

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