激酶
癌症研究
小分子
共济失调毛细血管扩张
癌症治疗
化学
癌症
药理学
生物
DNA损伤
生物化学
DNA
遗传学
作者
Yan A. Ivanenkov,А. В. Малышев,Victor A. Terentiev,Anastasia A. Korzhenevskaya,Sergei Evteev,Sergey Z. Vatsadze,Алексей В. Медведько,П. В. Шегай,А. Д. Каприн
标识
DOI:10.1080/13543776.2024.2446228
摘要
ATM kinase is a promising target for cancer therapy. Small-molecule ATM kinase inhibitors hold significant potential in cancer treatment by enhancing the efficacy of existing DNA-damaging therapies. Patent analysis revealed that the majority of these compounds contain imidazo[4,5-c]quinolinone scaffold or its bioisosteric variations which are optimal in terms of good ATM inhibitory activity and selectivity over closely related enzymes. Clinical trials explore combinations with RT or DNA-targeted compounds like PARP inhibitors, which induce DSBs. The medicinal chemistry field anticipates that these therapeutic options will soon be available on the pharmaceutical market.
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