Synthesis and activity of novel 16-dehydropregnenolone acetate derivatives as inhibitors of type 1 5α-reductase and on cancer cell line SK-LU-1.

MLA

Silva-Ortiz, Aylin Viviana, et al. “Synthesis and Activity of Novel 16-Dehydropregnenolone Acetate Derivatives as Inhibitors of Type 1 5α-Reductase and on Cancer Cell Line SK-LU-1.” Bioorganic & Medicinal Chemistry, vol. 23, no. 24, Dec. 2015, pp. 7535–42. EBSCOhost, https://doi.org/10.1016/j.bmc.2015.10.047.

APA

Silva-Ortiz, A. V., Bratoeff, E., Ramírez-Apan, T., Heuze, Y., Sánchez, A., Soriano, J., & Cabeza, M. (2015). Synthesis and activity of novel 16-dehydropregnenolone acetate derivatives as inhibitors of type 1 5α-reductase and on cancer cell line SK-LU-1. Bioorganic & Medicinal Chemistry, 23(24), 7535–7542. https://doi.org/10.1016/j.bmc.2015.10.047

Chicago

Silva-Ortiz, Aylin Viviana, Eugene Bratoeff, Teresa Ramírez-Apan, Yvonne Heuze, Araceli Sánchez, Juan Soriano, and Marisa Cabeza. 2015. “Synthesis and Activity of Novel 16-Dehydropregnenolone Acetate Derivatives as Inhibitors of Type 1 5α-Reductase and on Cancer Cell Line SK-LU-1.” Bioorganic & Medicinal Chemistry 23 (24): 7535–42. doi:10.1016/j.bmc.2015.10.047.