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Chemmedchem|June 21, 2013
Design of a highly selective and potent class of non-planar estrogen receptor β agonistsHenrik Sundén, Jian-Nong Ma, Lars K Hansen, et al.Chemmedchem|June 25, 2013
Characterization of the stereochemical structures of 2H-thiazolo[3,2-a]pyrimidine compounds and their binding affinities for anti-apoptotic Bcl-2 family proteinsYaochun Xu, Mi Zhou, Yan Li, et al.Chemmedchem|June 20, 2013
E-64c-hydrazide: a lead structure for the development of irreversible cathepsin C inhibitorsHanna Radzey, Markus Rethmeier, Dennis Klimpel, et al.Chemmedchem|July 10, 2013
Discovery of an acyclic nucleoside phosphonate that inhibits Mycobacterium tuberculosis ThyX based on the binding mode of a 5-alkynyl substrate analogueAnastasia Parchina, Matheus Froeyen, Lia Margamuljana, et al.Chemmedchem|July 2, 2013
Identification of Hck inhibitors as hits for the development of antileukemia and anti-HIV agentsCristina Tintori, Ilaria Laurenzana, Francesco La Rocca, et al.Chemmedchem|April 10, 2013
Small-molecule regulators of autophagy and their potential therapeutic applicationsMi Zhou, Renxiao WangChemmedchem|April 12, 2013
Design, synthesis, and antibacterial activity of demethylvancomycin analogues against drug-resistant bacteriaJun Chang, Si-Ji Zhang, Yong-Wei Jiang, et al.Chemmedchem|May 10, 2013
Optimization of triazine nitriles as rhodesain inhibitors: structure-activity relationships, bioisosteric imidazopyridine nitriles, and X-ray crystal structure analysis with human cathepsin LVeronika Ehmke, Edwin Winkler, David W Banner, et al.Chemmedchem|April 30, 2013
5'-Trityl-substituted thymidine derivatives as a novel class of antileishmanial agents: Leishmania infantum EndoG as a potential targetElena Casanova, David Moreno, Alba Gigante, et al.Chemmedchem|March 6, 2012
Bulbispermine: a crinine-type Amaryllidaceae alkaloid exhibiting cytostatic activity toward apoptosis-resistant glioma cellsGiovanni Luchetti, Robert Johnston, Véronique Mathieu, et al.Pageof 461