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European Journal of Medicinal Chemistry|October 30, 2015
Tryptophan dendrimers that inhibit HIV replication, prevent virus entry and bind to the HIV envelope glycoproteins gp120 and gp41Eva Rivero-Buceta, Elisa G Doyagüez, Ignacio Colomer, et al.Bioorganic & Medicinal Chemistry|June 8, 2013
Synthesis and anti-HCMV activity of 1-[ω-(phenoxy)alkyl]uracil derivatives and analogues thereofMikhail S Novikov, Denis A Babkov, Maria P Paramonova, et al.Journal of Medicinal Chemistry|February 18, 2005
Novel [2',5'-bis-O-(tert-butyldimethylsilyl)-beta-D-ribofuranosyl]- 3'-spiro-5''-(4''-amino-1'',2''-oxathiole-2'',2" -dioxide) derivatives with anti-HIV-1 and anti-human-cytomegalovirus activitySonia de Castro, Esther Lobatón, María-Jesús Pérez-Pérez, et al.Journal of Medicinal Chemistry|February 4, 2005
Synthesis, X-ray crystal structure study, and cytostatic and antiviral evaluation of the novel cycloalkyl-N-aryl-hydroxamic acidsMonika Barbarić, Stanko Ursić, Viktor Pilepić, et al.Journal of Medicinal Chemistry|February 15, 2007
Synthesis and preliminary evaluation of 18F- or 11C-labeled bicyclic nucleoside analogues as potential probes for imaging varicella-zoster virus thymidine kinase gene expression using positron emission tomographySatish K Chitneni, Christophe M Deroose, Jan Balzarini, et al.Journal of Medicinal Chemistry|June 7, 2014
Organometallic nucleoside analogues with ferrocenyl linker groups: synthesis and cancer cell line studiesHuy V Nguyen, Antoine Sallustrau, Jan Balzarini, et al.Bioorganic & Medicinal Chemistry Letters|March 3, 2009
Hybrid alpha-bromoacryloylamido chalcones. Design, synthesis and biological evaluationRomeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carrion, et al.Bioorganic & Medicinal Chemistry|May 12, 2009
2-(3-Aryl-2-propenoyl)-3-methylquinoxaline-1,4-dioxides: a novel cluster of tumor-specific cytotoxins which reverse multidrug resistanceUmashankar Das, Hari N Pati, Atulya K Panda, et al.Molecular Cancer Therapeutics|February 4, 2012
The thymidine phosphorylase inhibitor 5'-O-tritylinosine (KIN59) is an antiangiogenic multitarget fibroblast growth factor-2 antagonistSandra Liekens, Annelies Bronckaers, Mirella Belleri, et al.Bioorganic & Medicinal Chemistry|April 22, 2008
Synthesis, cytostatic and anti-HIV evaluations of the new unsaturated acyclic C-5 pyrimidine nucleoside analoguesTatjana Gazivoda, Silvana Raić-Malić, Vedran Kristafor, et al.Pageof 68