胰腺癌
生物信息学
表面等离子共振
化学
对接(动物)
体外
三唑
溶解度
癌细胞
药理学
癌症研究
生物化学
组合化学
癌症
生物
医学
纳米技术
纳米颗粒
内科学
材料科学
有机化学
基因
护理部
作者
Haijun Gu,Ting Zhang,Yunqi Li,Yuan He,Tian Guan,Weiqiong Kan,Peng He,Zhengfang Yi,Yihua Chen
标识
DOI:10.4155/fmc-2022-0168
摘要
Aim: The first inhibitor targeting myoferlin (MYOF), WJ460, bears poor metabolic stability and water solubility. Therefore, this study aimed to improve the drug-like properties of WJ460. Materials & methods: The authors synthesized an array of 1,5-diaryl-1,2,4-triazole analogs and appraised the binding activities with MYOF and their antiproliferative and antimigratory activities against pancreatic cancer cells. Results: Molecular docking and surface plasmon resonance results showed that E4 was directly bound to the MYOF-C2D domain. E4 effectively inhibited the proliferation and migration of pancreatic cancer cells in vitro. An in silico study suggested that the water solubility of E4 was improved by about 22-times than that of WJ460. Conclusion: The findings suggested that the druglike ability of E4 was significantly improved.
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