Macrocyclic ureas as potent and selective Chk1 inhibitors: an improved synthesis, kinome profiling, structure-activity relationships, and preliminary pharmacokinetics.

MLA

Tao, Zhi-Fu, et al. “Macrocyclic Ureas as Potent and Selective Chk1 Inhibitors: An Improved Synthesis, Kinome Profiling, Structure-Activity Relationships, and Preliminary Pharmacokinetics.” Bioorganic & Medicinal Chemistry Letters, vol. 17, no. 23, Dec. 2007, pp. 6593–601. EBSCOhost, https://doi.org/10.1016/j.bmcl.2007.09.063.

APA

Tao, Z.-F., Chen, Z., Bui, M.-H., Kovar, P., Johnson, E., Bouska, J., Zhang, H., Rosenberg, S., Sowin, T., & Lin, N.-H. (2007). Macrocyclic ureas as potent and selective Chk1 inhibitors: an improved synthesis, kinome profiling, structure-activity relationships, and preliminary pharmacokinetics. Bioorganic & Medicinal Chemistry Letters, 17(23), 6593–6601. https://doi.org/10.1016/j.bmcl.2007.09.063

Chicago

Tao, Zhi-Fu, Zehan Chen, Mai-Ha Bui, Peter Kovar, Eric Johnson, Jennifer Bouska, Haiying Zhang, Saul Rosenberg, Thomas Sowin, and Nan-Horng Lin. 2007. “Macrocyclic Ureas as Potent and Selective Chk1 Inhibitors: An Improved Synthesis, Kinome Profiling, Structure-Activity Relationships, and Preliminary Pharmacokinetics.” Bioorganic & Medicinal Chemistry Letters 17 (23): 6593–6601. doi:10.1016/j.bmcl.2007.09.063.