Synthesis, SAR and biological evaluation of 1,6-disubstituted-1H-pyrazolo[3,4-d]pyrimidines as dual inhibitors of Aurora kinases and CDK1

MLA

Le Brazidec, Jean-Yves, et al. “Synthesis, SAR and Biological Evaluation of 1,6-Disubstituted-1H-Pyrazolo[3,4-d]Pyrimidines as Dual Inhibitors of Aurora Kinases and CDK1.” Bioorganic & Medicinal Chemistry Letters, vol. 22, no. 5, Mar. 2012, pp. 2070–74. EBSCOhost, https://doi.org/10.1016/j.bmcl.2012.01.019.

APA

Le Brazidec, J.-Y., Pasis, A., Tam, B., Boykin, C., Black, C., Wang, D., Claassen, G., Chong, J.-H., Chao, J., Fan, J., Nguyen, K., Silvian, L., Ling, L., Zhang, L., Choi, M., Teng, M., Pathan, N., Zhao, S., Li, T., & Taveras, A. (2012). Synthesis, SAR and biological evaluation of 1,6-disubstituted-1H-pyrazolo[3,4-d]pyrimidines as dual inhibitors of Aurora kinases and CDK1. Bioorganic & Medicinal Chemistry Letters, 22(5), 2070–2074. https://doi.org/10.1016/j.bmcl.2012.01.019

Chicago

Le Brazidec, Jean-Yves, Angela Pasis, Betty Tam, Christina Boykin, Cheryl Black, Deping Wang, Gisela Claassen, et al. 2012. “Synthesis, SAR and Biological Evaluation of 1,6-Disubstituted-1H-Pyrazolo[3,4-d]Pyrimidines as Dual Inhibitors of Aurora Kinases and CDK1.” Bioorganic & Medicinal Chemistry Letters 22 (5): 2070–74. doi:10.1016/j.bmcl.2012.01.019.