溶解度
DNA
药物发现
计算机科学
化学
计算生物学
材料科学
医学
生物
生物化学
物理化学
作者
Zachary J. Waldrip,Baku Acharya,Daniel W. Armstrong,Maha Hanafi,Randall R. Rainwater,Sharon Amole,Madeline Fulmer,Ana Clara P. Azevedo‐Pouly,Alaina Burns,Lyle Burdine,Brendan Frett,Marie Schluterman Burdine
标识
DOI:10.1038/s41598-024-70858-w
摘要
DNA-dependent protein kinase catalytic subunit (DNA-PKcs) plays a vital role in DNA damage repair and lymphocyte function, presenting a significant target in cancer and immune diseases. Current DNA-PKcs inhibitors are undergoing Phase I/II trials as adjuncts to radiotherapy and chemotherapy in cancer. Nevertheless, clinical utility is limited by suboptimal bioavailability. This study introduces DNA-PKcs inhibitors designed to enhance bioavailability. We demonstrate that a novel DNA-PKcs inhibitor, DA-143, surpasses NU7441 in aqueous solubility as well as other available inhibitors. In addition, DA-143 displayed an improvement in DNA-PKcs inhibition relative to NU7441 achieving an IC
科研通智能强力驱动
Strongly Powered by AbleSci AI