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Synthesis of 26-hydroxy-22-oxocholestanic frameworks from diosgenin and hecogenin and their in vitro antiproliferative and apoptotic activity on human cervical cancer CaSki cells.
Fernández-Herrera MA, López-Muñoz H, Hernández-Vázquez JM, López-Dávila M, Escobar-Sánchez ML, Sánchez-Sánchez L, Pinto BM, Sandoval-Ramírez J. Fernández-Herrera MA, et al. Bioorg Med Chem. 2010 Apr 1;18(7):2474-84. doi: 10.1016/j.bmc.2010.02.051. Epub 2010 Mar 1. Bioorg Med Chem. 2010. PMID: 20303770
Synthesis of the steroidal glycoside (25R)-3β,16β-diacetoxy-12,22-dioxo-5α-cholestan-26-yl β-D-glucopyranoside and its anti-cancer properties on cervicouterine HeLa, CaSki, and ViBo cells.
Fernández-Herrera MA, Mohan S, López-Muñoz H, Hernández-Vázquez JM, Pérez-Cervantes E, Escobar-Sánchez ML, Sánchez-Sánchez L, Regla I, Pinto BM, Sandoval-Ramírez J. Fernández-Herrera MA, et al. Eur J Med Chem. 2010 Nov;45(11):4827-37. doi: 10.1016/j.ejmech.2010.07.051. Epub 2010 Aug 11. Eur J Med Chem. 2010. PMID: 20801554
Synthesis and biological evaluation of the glycoside (25R)-3β,16β-diacetoxy-22-oxocholest-5-en-26-yl β-d-glucopyranoside: a selective anticancer agent in cervicouterine cell lines.
Fernández-Herrera MA, López-Muñoz H, Hernández-Vázquez JM, López-Dávila M, Mohan S, Escobar-Sánchez ML, Sánchez-Sánchez L, Pinto BM, Sandoval-Ramírez J. Fernández-Herrera MA, et al. Eur J Med Chem. 2011 Sep;46(9):3877-86. doi: 10.1016/j.ejmech.2011.05.058. Epub 2011 May 30. Eur J Med Chem. 2011. PMID: 21703733
Synthesis and selective anticancer activity of steroidal glycoconjugates.
Fernández-Herrera MA, López-Muñoz H, Hernández-Vázquez JM, Sánchez-Sánchez L, Escobar-Sánchez ML, Pinto BM, Sandoval-Ramírez J. Fernández-Herrera MA, et al. Eur J Med Chem. 2012 Aug;54:721-7. doi: 10.1016/j.ejmech.2012.06.027. Epub 2012 Jun 21. Eur J Med Chem. 2012. PMID: 22770605
77 results