Showing results (51-60 of 179) with videos related to
Sort By:
Pageof 18
International Journal of Pharmaceutics|December 14, 2002
Enhanced transport of a novel anti-HIV agent--cosalane and its congeners across human intestinal epithelial (Caco-2) cell monolayersChandrasekhar Udata, Jignesh Patel, Dhananjay Pal, et al.Rapid Communications in Mass Spectrometry : RCM|July 23, 2003
The 'apparent' hydrolysis of alkyl esters during electrospray ionizationMaximilian A Silvestri, Deborah Miles, Arlene P Rothwell, et al.Rapid Communications in Mass Spectrometry : RCM|March 13, 2008
Hydrolysis of thioesters in an ion trapMatthew Cullen, Deborah Miles, Arlene Rothwell, et al.Journal of Medicinal Chemistry|February 13, 2014
Synthesis and biological evaluation of new carbohydrate-substituted indenoisoquinoline topoisomerase I inhibitors and improved syntheses of the experimental anticancer agents indotecan (LMP400) and indimitecan (LMP776)Daniel E Beck, Keli Agama, Christophe Marchand, et al.Journal of Medicinal Chemistry|July 22, 2005
Synthesis and mechanism of action studies of a series of norindenoisoquinoline topoisomerase I poisons reveal an inhibitor with a flipped orientation in the ternary DNA-enzyme-inhibitor complex as determined by X-ray crystallographic analysisAlexandra Ioanoviciu, Smitha Antony, Yves Pommier, et al.Journal of Natural Products|December 14, 2011
Induction of apoptosis by 3-amino-6-(3-aminopropyl)-5,6-dihydro-5,11-dioxo-11H-indeno[1,2-c]isoquinoline via modulation of MAPKs (p38 and c-Jun N-terminal kinase) and c-Myc in HL-60 human leukemia cellsEun-Jung Park, Evgeny Kiselev, Martin Conda-Sheridan, et al.Journal of Medicinal Chemistry|February 17, 2010
Structure-based design, synthesis, and biological studies of new anticancer norindenoisoquinoline topoisomerase I inhibitorsYunlong Song, Zhiyu Shao, Thomas S Dexheimer, et al.The Journal of Organic Chemistry|November 10, 2005
Design, synthesis, and biochemical evaluation of 1,5,6,7-tetrahydro-6,7-dioxo-9-D-ribitylaminolumazines bearing alkyl phosphate substituents as inhibitors of lumazine synthase and riboflavin synthaseMark Cushman, Guangyi Jin, Thota Sambaiah, et al.Journal of Medicinal Chemistry|January 19, 2007
Synthesis and cancer chemopreventive activity of zapotin, a natural product from Casimiroa edulisArup Maiti, Muriel Cuendet, Tamara Kondratyuk, et al.Plos One|October 3, 2013
Solvent dependency of the UV-Vis spectrum of indenoisoquinolines: role of keto-oxygens as polarity interaction probesAndrea Coletta, Silvia Castelli, Giovanni Chillemi, et al.Pageof 18