Cite
Design, synthesis and evaluation of C-5 substituted pyrrolopyridine derivatives as potent Janus Kinase 1 inhibitors with excellent selectivity.
MLA
Chen, Limei, et al. “Design, Synthesis and Evaluation of C-5 Substituted Pyrrolopyridine Derivatives as Potent Janus Kinase 1 Inhibitors with Excellent Selectivity.” European Journal of Medicinal Chemistry, vol. 267, Mar. 2024, p. N.PAG. EBSCOhost, https://doi.org/10.1016/j.ejmech.2024.116210.
APA
Chen, L., Tang, Y., Lang, J.-J., Lin, Y., Yu, Z., Li, X., Zheng, X., Mi, P., Lv, Y., & Lin, Y.-W. (2024). Design, synthesis and evaluation of C-5 substituted pyrrolopyridine derivatives as potent Janus Kinase 1 inhibitors with excellent selectivity. European Journal of Medicinal Chemistry, 267, N.PAG. https://doi.org/10.1016/j.ejmech.2024.116210
Chicago
Chen, Limei, Yahua Tang, Jia-Jia Lang, Yuqing Lin, Zhixin Yu, Xinhao Li, Xing Zheng, Pengbing Mi, You Lv, and Ying-Wu Lin. 2024. “Design, Synthesis and Evaluation of C-5 Substituted Pyrrolopyridine Derivatives as Potent Janus Kinase 1 Inhibitors with Excellent Selectivity.” European Journal of Medicinal Chemistry 267 (March): N.PAG. doi:10.1016/j.ejmech.2024.116210.