Universita degli Studi di Torino, Facolta di Farmacia, Dipartimento di Scienza e Tecnologia del Farmaco, Via P. Giuria 9, 10125 Torino, Italy.
Curr Top Med Chem. 2011;11(18):2346-81. doi: 10.2174/156802611797183221.
Research in anticancer chemotherapy has produced outstanding results, and mean survival rates have significantly improved over the last ten years. Nevertheless, all approved drugs are still characterized by narrow therapeutic windows that result mainly from their high systemic toxicity combined with their marked lack of tumor selectivity. Medicinal chemistry responds to the resulting demands with new analogues of a lead drug, or by developing prodrugs. Prodrugs are inactive compounds, which are metabolized in the body, either chemically or enzymatically, in a controlled or predictable manner, to the active parent drug. This review describes the results of strategies in prodrug development, subdivided into the principal categories of anticancer agents. The chemical implementation of prodrug approaches is illustrated through selected drug candidates.
在抗癌化疗的研究中取得了杰出的成果,在过去十年中,平均存活率有了显著提高。然而,所有批准的药物仍然具有狭窄的治疗窗口,这主要是由于它们的高全身毒性,加上它们明显缺乏肿瘤选择性。药物化学通过先导药物的新类似物或通过开发前药来应对由此产生的需求。前药是无活性的化合物,在体内通过化学或酶促方式以受控或可预测的方式代谢为活性母体药物。本综述描述了前药开发策略的结果,分为主要类别的抗癌药物。通过选择的候选药物说明了前药方法的化学实施。