Ma, T., Pusch, S., & Deimling, A. v. (2017). Design, synthesis and biological activity of 3-pyrazine-2-yl-oxazolidin-2-ones as novel, potent and selective inhibitors of mutant isocitrate dehydrogenase 1. Bioorganic & medicinal chemistry, 25(24), . https://doi.org/10.1016/j.bmc.2017.10.009
Chicago-Zitierstil (17. Ausg.)Ma, Tianfang, Stefan Pusch, und Andreas von Deimling. "Design, Synthesis and Biological Activity of 3-pyrazine-2-yl-oxazolidin-2-ones as Novel, Potent and Selective Inhibitors of Mutant Isocitrate Dehydrogenase 1." Bioorganic & Medicinal Chemistry 25, no. 24 (2017). https://doi.org/10.1016/j.bmc.2017.10.009.
MLA-Zitierstil (9. Ausg.)Ma, Tianfang, et al. "Design, Synthesis and Biological Activity of 3-pyrazine-2-yl-oxazolidin-2-ones as Novel, Potent and Selective Inhibitors of Mutant Isocitrate Dehydrogenase 1." Bioorganic & Medicinal Chemistry, vol. 25, no. 24, 2017, https://doi.org/10.1016/j.bmc.2017.10.009.