化学
阿霉素
二肽
紫杉醇
前药
丝裂霉素C
药理学
组织蛋白酶D
赫拉
去肽
酶抑制剂
体外
药品
化疗
生物化学
肽
酶
内科学
外科
医学
作者
Gene M. Dubowchik,Kathleen Mosure,Jay O. Knipe,Raymond A. Firestone
标识
DOI:10.1016/s0960-894x(98)00610-6
摘要
Substrates containing doxorubicin (DOX), paclitaxel (taxol®), and mitomycin C (MMC) attached to the cathepsin B-sensitive dipeptide Phe-Lys via a self-immolative spacer were prepared as model compounds for internalizing anticancer immunoconjugates. Cathepsin B-mediated release rates of free drug, rat liver lysosomal susceptibility and human plasma stability were measured for each.
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