作者:Vivekananda M. Vrudhula、John F. MacMaster、Zhengong Li、David E. Kerr、Peter D. Senter
DOI:10.1016/s0960-894x(02)00784-9
日期:2002.12
A series of unsymmetrical polar disulfide prodrugs 2-5 of paclitaxel were designed and synthesized as reductively activated prodrugs. These compounds behaved as prodrugs in vitro on L2987 lung carcinoma cells. In vivo evaluation in mice demonstrated that the mutual prodrug 5 with captopril exhibited significant regressions and cures.
设计并合成了一系列紫杉醇不对称极性二硫化物前药2-5,并将其合成为还原活化前药。这些化合物在体外对L2987肺癌细胞具有前药作用。小鼠体内评估表明,与卡托普利的互用前药5表现出明显的消退和治愈作用。