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Design of BET Inhibitor Prodrugs with Superior Efficacy and Devoid of Systemic Toxicities
[post]
2020
unpublished
<div><p>Prodrugs engineered for preferential activation in diseased versus normal tissues offer immense potential to improve the therapeutic index of preclinical and clinical-stage active pharmaceutical ingredients that either cannot be developed otherwise or whose efficacy or tolerability it is highly desirable to improve. Such approaches, however, often suffer from trial-and-error design, precluding predictive design and optimization. Here, using BET bromodomain inhibitors (BETi)—a class of
doi:10.26434/chemrxiv.13241966.v1
fatcat:h2my3vqxgzbzpkcixie7p6shri