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Organic & Biomolecular Chemistry|October 11, 2012
Synthesis, biological evaluation, and structure-activity relationships of tri- and tetrasubstituted olefins related to isocombretastatin A-4 as new tubulin inhibitorsJessy Aziz, Etienne Brachet, Abdallah Hamze, et al.Molecular Endocrinology (Baltimore, Md.)|April 13, 2013
A new strategy for selective targeting of progesterone receptor with passive antagonistsJunaid A Khan, Abdellatif Tikad, Michel Fay, et al.Scientific Reports|November 24, 2016
Characterization of the Annonaceous acetogenin, annonacinone, a natural product inhibitor of plasminogen activator inhibitor-1Stéphane Pautus, Mouad Alami, Fréderic Adam, et al.Human Molecular Genetics|July 31, 2012
Hsp90 stabilizes Cdc25A and counteracts heat shock-mediated Cdc25A degradation and cell-cycle attenuation in pancreatic carcinoma cellsBenedikt Giessrigl, Sigurd Krieger, Margit Rosner, et al.European Journal of Medicinal Chemistry|December 5, 2017
A fluorine scan of a tubulin polymerization inhibitor isocombretastatin A-4: Design, synthesis, molecular modelling, and biological evaluationTimothée Naret, Jérôme Bignon, Guillaume Bernadat, et al.Journal of Medicinal Chemistry|July 14, 2018
Design and Synthesis of Tubulin and Histone Deacetylase Inhibitor Based on iso-Combretastatin A-4Diana Lamaa, Hsin-Ping Lin, Lena Zig, et al.European Journal of Medicinal Chemistry|July 7, 2022
Design, synthesis and biological evaluation of quinoline-2-carbonitrile-based hydroxamic acids as dual tubulin polymerization and histone deacetylases inhibitorsCamille Hauguel, Sarah Ducellier, Olivier Provot, et al.Pageof 10