表皮生长因子受体
对接(动物)
码头
三唑
化学
IC50型
立体化学
激酶
组合化学
生长因子受体
生物化学
药理学
受体
生物
体外
医学
有机化学
护理部
作者
Abel Kolawole Oyebamiji,Sunday Adewale Akintelu,Oreoluwa P. Amao,Mary Oluwatosin Kaka,Adetoun Elizabeth Morakinyo,Folake Ayobami Amao,Banjo Semire
出处
期刊:Data in Brief
[Elsevier BV]
日期:2021-06-17
卷期号:37: 107234-107234
被引量:13
标识
DOI:10.1016/j.dib.2021.107234
摘要
Data from eight 1,2,4-thiadiazole-1,2,4-triazole derivatives were used to observe the anti-epidermal growth factor receptor kinase activities of 1,2,4-thiadiazole-1,2,4-triazole analogues thereby reducing human lung cancer. The software used to achieve this work were Spartan 14, Pymol, mgltools_win32_1.5.6, Auto dock vina and biovia2019.ds2019client. Also, the developed QSAR model was developed using the screened descriptors so as to inspect the closeness between the experimental IC50 and the predicted IC50. More so, the binding affinity from 1,2,4-thiadiazole-1,2,4-triazole derivatives - epidermal growth factor receptor kinase complexes using molecular docking approach were reported. Also, the ADMET properties for selected compounds and proposed compounds with better binding affinity were reported.
科研通智能强力驱动
Strongly Powered by AbleSci AI