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Potent Triazole Bisphosphonate Inhibitor of Geranylgeranyl Diphosphate Synthase

机译:香叶基香叶基二磷酸合酶的强效三唑双膦酸酯抑制剂

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摘要

Studies of triazole bisphosphonates have resulted in identification of a potent inhibitor of geranylgeranyl diphosphate synthase (IC50 = 45 nM) with very good selectivity for this enzyme over farnesyl diphosphate synthase (IC50 = 28 mu M). This compound also potently disrupts geranylgeranylation and induces cytotoxicity in human myeloma cells at submicromolar levels, suggesting that it may serve as a lead compound for treatment of malignancies characterized by excessive protein secretion.
机译:对三唑双膦酸酯的研究已经鉴定出一种强力的香叶基香叶基二磷酸合酶(IC50 = 45 nM)抑制剂,相对于法呢基二磷酸合酶(IC50 = 28μM)具有很好的选择性。该化合物还以亚微摩尔水平有效地破坏香叶基香叶基化,并在人骨髓瘤细胞中诱导细胞毒性,表明它可以作为治疗以蛋白质分泌过多为特征的恶性肿瘤的先导化合物。

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