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Archiv Der Pharmazie|December 5, 2012
Biological evaluation of androstene derivativesMariana Garrido, Eugene Bratoeff, Mario García-Lorenzana, et al.The Journal of Steroid Biochemistry and Molecular Biology|July 16, 2008
Synthesis and biological effect of halogen substituted phenyl acetic acid derivatives of progesterone as potent progesterone receptor antagonistsMarisa Cabeza, Eugene Bratoeff, Georgina Gómez, et al.Steroids|May 13, 2008
Biological activity of novel progesterone derivatives having a bulky ester side chains at C-3Marisa Cabeza, Eugene Bratoeff, Elena Ramírez, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|February 19, 2015
Biological activity of pyrazole and imidazole-dehydroepiandrosterone derivatives on the activity of 17β-hydroxysteroid dehydrogenaseMarisa Cabeza, Alejandro Posada, Araceli Sánchez-Márquez, et al.The Journal of Steroid Biochemistry and Molecular Biology|July 17, 2007
Steroids with a carbamate function at C-17, a novel class of inhibitors for human and hamster steroid 5alpha-reductaseEugene Bratoeff, Teresita Sainz, Marisa Cabeza, et al.Chemical & Pharmaceutical Bulletin|December 6, 2005
Synthesis and pharmacological evaluation of new progesterone esters as 5alpha-reductase inhibitorsElena Ramírez, Marisa Cabeza, Eugene Bratoeff, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|September 24, 2015
Novel dehydroepiandrosterone benzimidazolyl derivatives as 5α-reductase isozymes inhibitorsYazmín Arellano, Eugene Bratoeff, Tania Segura, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|October 25, 2006
New progesterone derivatives as inhibitors of 5alpha-reductase enzyme and prostate cancer cell growthMarisa Cabeza, Eugene Bratoeff, Ivonne Heuze, et al.Bioorganic & Medicinal Chemistry|February 9, 2017
Synthesis of new derivatives of 21-imidazolyl-16-dehydropregnenolone as inhibitors of 5α-reductase 2 and with cytotoxic activity in cancer cellsAylin Viviana Silva-Ortiz, Eugene Bratoeff, Teresa Ramírez-Apan, et al.Pageof 5