Cite
Discovery of 7H-pyrrolo[2,3-d]pyridine derivatives as potent FAK inhibitors: Design, synthesis, biological evaluation and molecular docking study.
MLA
Wang, Ruifeng, et al. “Discovery of 7H-Pyrrolo[2,3-d]Pyridine Derivatives as Potent FAK Inhibitors: Design, Synthesis, Biological Evaluation and Molecular Docking Study.” Bioorganic Chemistry, vol. 102, Sept. 2020, p. N.PAG. EBSCOhost, https://doi.org/10.1016/j.bioorg.2020.104092.
APA
Wang, R., Zhao, X., Yu, S., Chen, Y., Cui, H., Wu, T., Hao, C., Zhao, D., & Cheng, M. (2020). Discovery of 7H-pyrrolo[2,3-d]pyridine derivatives as potent FAK inhibitors: Design, synthesis, biological evaluation and molecular docking study. Bioorganic Chemistry, 102, N.PAG. https://doi.org/10.1016/j.bioorg.2020.104092
Chicago
Wang, Ruifeng, Xiangxin Zhao, Sijia Yu, Yixuan Chen, Hengxian Cui, Tianxiao Wu, Chenzhou Hao, Dongmei Zhao, and Maosheng Cheng. 2020. “Discovery of 7H-Pyrrolo[2,3-d]Pyridine Derivatives as Potent FAK Inhibitors: Design, Synthesis, Biological Evaluation and Molecular Docking Study.” Bioorganic Chemistry 102 (September): N.PAG. doi:10.1016/j.bioorg.2020.104092.