化学
结合
连接器
体内
酒
组合化学
药品
共轭体系
葡萄糖醛酸
乙醇
内化
体外
烷氧基
抗体
药理学
生物化学
有机化学
免疫学
新陈代谢
生物技术
数学分析
操作系统
生物
聚合物
细胞
医学
烷基
计算机科学
数学
作者
Robert V. Kolakowski,Karl T. Haelsig,Kim K. Emmerton,Chris Leiske,Jamie B. Miyamoto,Julia H. Cochran,Robert P. Lyon,Peter D. Senter,Scott C. Jeffrey
标识
DOI:10.1002/anie.201601506
摘要
Abstract A strategy for the conjugation of alcohol‐containing payloads to antibodies has been developed and involves the methylene alkoxy carbamate (MAC) self‐immolative unit. A series of MAC β‐glucuronide model constructs were prepared to evaluate stability and enzymatic release, and the results demonstrated high stability at physiological pH in a substitution‐dependent manner. All the MAC model compounds efficiently released alcohol drug surrogates under the action of β‐glucuronidase. To assess the MAC technology for ADCs, the potent microtubule‐disrupting agent auristatin E (AE) was incorporated through the norephedrine alcohol. Conjugation of the MAC β‐glucuronide AE drug linker to the anti‐CD30 antibody cAC10, and an IgG control antibody, gave potent and immunologically specific activities in vitro and in vivo. These studies validate the MAC self‐immolative unit for alcohol‐containing payloads within ADCs, a class that has not been widely exploited.
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