化学
连接器
半胱氨酸
组合化学
药理学
生物化学
计算机科学
医学
操作系统
酶
作者
J. Q. You,Juan Zhang,Jun Wang,Mingzhi Jin
标识
DOI:10.1021/acs.bioconjchem.1c00213
摘要
Antibody–drug conjugates (ADCs) have attracted great attention in recent years in the wake of an accelerated FDA approval rate and several large-scale acquisitions. To date, there are ten ADC drugs on the market and more than 70 in various stages of clinical trials. Yet, due to the complicated nature of ADC molecules, considerations need to cover many aspects for the success of ADCs, including target specificity, linker–payload stability, tumor permeability, and clearance rate. This topical review summarizes and discusses current methods used to increase stability and homogeneity of ADCs of cysteine conjugation. We believe that they will lead to improvement of efficacy and pharmacokinetics (PK) of ADC drugs.
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