奥西默替尼
T790米
肺癌
癌症研究
电泳剂
突变
医学
化学
肿瘤科
基因
癌症
内科学
腺癌
生物化学
ROS1型
催化作用
作者
Harun Patel,Iqrar Ahmad,Harsha Jadhav,Rahul Pawara,Deepak K. Lokwani,Sanjay J. Surana
标识
DOI:10.2174/1386207323666201204125524
摘要
BACKGROUND: Lung cancer has become the prominent cause of the cancer-related deaths globally. More than 80 % of all lung cancers have been diagnosed with Non- Small Cell Lung Cancer (NSCLC). The USFDA approved osimertinib to treat patients with metastatic T790M EGFR NSCLC on a regular basis in March 2017. Recently, C797S mutation to osimertinib has been reported, which indicates the need for structural modification to overcome the problem of mutation. METHODS: In this bioinformatics study, we have evaluated the impact of various acrylamide as an electrophilic warhead on the activity and selectivity of osimertinib. RESULT: Osimertinib analouge 48, 50, 60, 61, 67, 75, 80, 86, 89, 92, 93, 116 and 124 were the most active and selective compounds against T790M EGFR mutants compared to Osimertinib. CONCLUSION: These compounds also showed less inclination towards WT-EGFR.
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