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Molecules (Basel, Switzerland)|January 31, 2017
Essential Oil Extraction, Chemical Analysis and Anti-Candida Activity of Calamintha nepeta (L.) Savi subsp. glandulosa (Req.) Ball-New ApproachesMijat Božović, Stefania Garzoli, Manuela Sabatino, et al.Journal of Chemical Information and Modeling|October 14, 2021
Human Estrogen Receptor α Antagonists. Part 1: 3-D QSAR-Driven Rational Design of Innovative Coumarin-Related Antiestrogens as Breast Cancer Suppressants through Structure-Based and Ligand-Based StudiesNezrina Mihović, Nevena Tomašević, Sanja Matić, et al.European Journal of Medicinal Chemistry|October 28, 2021
Human estrogen receptor α antagonists, part 2: Synthesis driven by rational design, in vitro antiproliferative, and in vivo anticancer evaluation of innovative coumarin-related antiestrogens as breast cancer suppressantsNezrina Kurtanović, Nevena Tomašević, Sanja Matić, et al.European Journal of Medicinal Chemistry|March 6, 2017
Enhancing activity and selectivity in a series of pyrrol-1-yl-1-hydroxypyrazole-based aldose reductase inhibitors: The case of trifluoroacetylationNikolaos Papastavrou, Maria Chatzopoulou, Jana Ballekova, et al.Journal of Medicinal Chemistry|September 29, 2006
Synthesis and biological properties of novel, uracil-containing histone deacetylase inhibitorsAntonello Mai, Silvio Massa, Dante Rotili, et al.Journal of Medicinal Chemistry|March 5, 2004
3-(4-Aroyl-1-methyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides as a new class of synthetic histone deacetylase inhibitors. 3. Discovery of novel lead compounds through structure-based drug design and docking studiesRino Ragno, Antonello Mai, Silvio Massa, et al.Journal of Medicinal Chemistry|April 19, 2002
Binding mode analysis of 3-(4-benzoyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamide: a new synthetic histone deacetylase inhibitor inducing histone hyperacetylation, growth inhibition, and terminal cell differentiationAntonello Mai, Silvio Massa, Rino Ragno, et al.European Journal of Medicinal Chemistry|February 24, 2005
Synthesis and evaluation of new tripeptide phosphonate inhibitors of MMP-8 and MMP-2Mariangela Agamennone, Cristina Campestre, Serena Preziuso, et al.Journal of Medicinal Chemistry|February 6, 2004
Computer-aided design, synthesis, and anti-HIV-1 activity in vitro of 2-alkylamino-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as novel potent non-nucleoside reverse transcriptase inhibitors, also active against the Y181C variantRino Ragno, Antonello Mai, Gianluca Sbardella, et al.The International Journal of Biochemistry & Cell Biology|October 7, 2008
New pyrrole-based histone deacetylase inhibitors: binding mode, enzyme- and cell-based investigationsAntonello Mai, Sergio Valente, Angela Nebbioso, et al.Pageof 15