首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >Novel furfurylidene N-acylhydrazones derived from natural safrole: discovery of LASSBio-1215, a new potent antiplatelet prototype
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Novel furfurylidene N-acylhydrazones derived from natural safrole: discovery of LASSBio-1215, a new potent antiplatelet prototype

机译:新型糠醛N-酰基腙源自天然脱脂:莱斯比奥1215的发现,一种新型效力抗血小板原型

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We describe herein the discovery of (E)-N-methyl-N’-((5-nitrofuran-2-yl)methylene)benzo[d] 1, 3 dioxole-5-carbohydrazide (9e), named LASSBio-1215, as a novel antiplatelet agent belonging to the N-methyl-N-acylhydrazone class, which exert their antiaggregating actions on human and rabbit platelets induced by different agonists, through cyclooxygenase-1 (COX-1) or thromboxane synthase inhibition. This compound was elected after screening of a series of functionalized furyl N-acylhydrazone derivatives, synthesized from natural safrole 10. In vitro assays showed that compound 9e presents platelet-aggregating activity in rabbit platelet-rich plasma (PRP) induced by arachidonic acid (IC50?=?0.7 μM) and collagen (IC50?=?4.5 μM). Moreover, LASSBio-1215 also inhibited almost completely the second wave of adenosine diphosphate-induced platelet aggregation in human PRP, and this effect was correlated with their ability to block the production of pro-aggregating autacoid thromboxane A2.
机译:我们在此描述(E)-N-甲基-N' - ((5-硝基呋喃-2-基)亚甲基)苯并[d] 1,3 二恶英-5-碳水化肼(9e “名为Lassbio-1215”,作为属于N-甲基-N-酰基腙类的新型抗血小板剂,其在不同激动剂诱导的人和兔血小板上施加由不同激动剂,通过环氧氢酶-1(COX-1)或血栓素(血栓滤蛋)施加其对人和兔血小板的抗凝集作用合成酶抑制。在筛选一系列官能化呋喃基衍生物之后选举该化合物,从天然脱胶10中合成。体外测定显示化合物9e呈现富含兔血小板血小板(PRP)的血小板聚集活性(IC 50 ?=?0.7μm)和胶原(IC 50 ?=Δ4.5μm)。此外,Lassbio-1215还抑制了人PRP中的几乎完全是腺苷二磷酸二磷酸诱导的血小板聚集的第二波,并且这种效果与它们阻断促粒性自身血管偶联X / Sub的产生的能力相关。

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