Cite
Structure-based design, synthesis and biological evaluation of aminopyrazines as highly potent, selective, and cellularly active allosteric SHP2 inhibitors.
MLA
Tang, Kai, et al. “Structure-Based Design, Synthesis and Biological Evaluation of Aminopyrazines as Highly Potent, Selective, and Cellularly Active Allosteric SHP2 Inhibitors.” European Journal of Medicinal Chemistry, vol. 230, Feb. 2022, p. N.PAG. EBSCOhost, https://doi.org/10.1016/j.ejmech.2022.114106.
APA
Tang, K., Zhao, M., Wu, Y.-H., Wu, Q., Wang, S., Dong, Y., Yu, B., Song, Y., & Liu, H.-M. (2022). Structure-based design, synthesis and biological evaluation of aminopyrazines as highly potent, selective, and cellularly active allosteric SHP2 inhibitors. European Journal of Medicinal Chemistry, 230, N.PAG. https://doi.org/10.1016/j.ejmech.2022.114106
Chicago
Tang, Kai, Min Zhao, Ya-Hong Wu, Qiong Wu, Shu Wang, Yu Dong, Bin Yu, Yihui Song, and Hong-Min Liu. 2022. “Structure-Based Design, Synthesis and Biological Evaluation of Aminopyrazines as Highly Potent, Selective, and Cellularly Active Allosteric SHP2 Inhibitors.” European Journal of Medicinal Chemistry 230 (February): N.PAG. doi:10.1016/j.ejmech.2022.114106.