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Discovery and Characterization of a Water-Soluble Prodrug of a Dual Inhibitor of Bacterial DNA Gyrase and Topoisomerase IV

ACS medicinal chemistry letters(2015)SCI 3区SCI 2区

Vertex Pharmaceut Inc | Hartford Hosp

Cited 22|Views46
Abstract
Benzimidazole 1 is the lead compound resulting from an antibacterial program targeting dual inhibitors of bacterial DNA gyrase and topoisomerase IV. With the goal of improving key drug-like properties, namely, the solubility and the formulability of 1, an effort to identify prodrugs was undertaken. This has led to the discovery of a phosphate ester prodrug 2. This prodrug is rapidly cleaved to the parent drug molecule upon both oral and intravenous administration. The prodrug achieved equivalent exposure of 1 compared to dosing the parent in multiple species. The prodrug 2 has improved aqueous solubility, simplifying both intravenous and oral formulation.
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Prodrug,DNA gyrase,topoisomerase IV,water soluble
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要点】:本研究发现了一种水溶性前药,能双重抑制细菌DNA旋转酶和拓扑异构酶IV,提高了药物的可溶性和可配方性。

方法】:通过对抗菌项目中的先导化合物苯并咪唑1进行结构改造,合成了磷酸酯前药2。

实验】:在口服和静脉给药后,前药2迅速裂解为母体药物1,并在多种物种中达到与直接给药母体药物相当的暴露量。使用的数据集未在文本中提及。前药2的水溶性得到改善,简化了静脉和口服制剂的制备。