SAR studies on tetrahydroisoquinoline derivatives: the role of flexibility and bioisosterism to raise potency and selectivity toward P-glycoprotein.

MLA

Capparelli, Elena, et al. “SAR Studies on Tetrahydroisoquinoline Derivatives: The Role of Flexibility and Bioisosterism to Raise Potency and Selectivity toward P-Glycoprotein.” Journal of Medicinal Chemistry, vol. 57, no. 23, Dec. 2014, pp. 9983–94. EBSCOhost, https://doi.org/10.1021/jm501640e.

APA

Capparelli, E., Zinzi, L., Cantore, M., Contino, M., Perrone, M. G., Luurtsema, G., Berardi, F., Perrone, R., & Colabufo, N. A. (2014). SAR studies on tetrahydroisoquinoline derivatives: the role of flexibility and bioisosterism to raise potency and selectivity toward P-glycoprotein. Journal of Medicinal Chemistry, 57(23), 9983–9994. https://doi.org/10.1021/jm501640e

Chicago

Capparelli, Elena, Laura Zinzi, Mariangela Cantore, Marialessandra Contino, Maria Grazia Perrone, Gert Luurtsema, Francesco Berardi, Roberto Perrone, and Nicola A Colabufo. 2014. “SAR Studies on Tetrahydroisoquinoline Derivatives: The Role of Flexibility and Bioisosterism to Raise Potency and Selectivity toward P-Glycoprotein.” Journal of Medicinal Chemistry 57 (23): 9983–94. doi:10.1021/jm501640e.