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Journal of Medicinal Chemistry|November 25, 2014
N-Methyl-N-((1-methyl-5-(3-(1-(2-methylbenzyl)piperidin-4-yl)propoxy)-1H-indol-2-yl)methyl)prop-2-yn-1-amine, a new cholinesterase and monoamine oxidase dual inhibitorOscar M Bautista-Aguilera, Abdelouahid Samadi, Mourad Chioua, et al.Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|April 15, 2015
SI113, a specific inhibitor of the Sgk1 kinase activity that counteracts cancer cell proliferationLucia D'Antona, Rosario Amato, Cristina Talarico, et al.European Journal of Medicinal Chemistry|January 13, 2023
8-Amide and 8-carbamate substitution patterns as modulators of 7-hydroxy-4-methylcoumarin's antidepressant profile: Synthesis, biological evaluation and docking studiesMaria J Matos, Paula Novo, Lucía Mayán, et al.ACS Medicinal Chemistry Letters|October 23, 2018
Tuning the Dual Inhibition of Carbonic Anhydrase and Cyclooxygenase by Dihydrothiazole BenzensulfonamidesRita Meleddu, Simona Distinto, Filippo Cottiglia, et al.Chemmedchem|May 23, 2014
Design, synthesis, and biological evaluation of 1,3-diarylpropenones as dual inhibitors of HIV-1 reverse transcriptaseRita Meleddu, Valeria Cannas, Simona Distinto, et al.Chemmedchem|September 29, 2011
Docking analysis and resistance evaluation of clinically relevant mutations associated with the HIV-1 non-nucleoside reverse transcriptase inhibitors nevirapine, efavirenz and etravirineStefano Alcaro, Claudia Alteri, Anna Artese, et al.Journal of Medicinal Chemistry|July 15, 2011
New insight into the central benzodiazepine receptor-ligand interactions: design, synthesis, biological evaluation, and molecular modeling of 3-substituted 6-phenyl-4H-imidazo[1,5-a][1,4]benzodiazepines and related compoundsMaurizio Anzini, Salvatore Valenti, Carlo Braile, et al.Oncotarget|October 14, 2015
Preclinical model in HCC: the SGK1 kinase inhibitor SI113 blocks tumor progression in vitro and in vivo and synergizes with radiotherapyCristina Talarico, Lucia D'Antona, Domenica Scumaci, et al.ACS Chemical Biology|May 1, 2013
Discovery of PTPRJ agonist peptides that effectively inhibit in vitro cancer cell proliferation and tube formationFrancesco Ortuso, Francesco Paduano, Alfonso Carotenuto, et al.ACS Chemical Biology|July 5, 2012
Isolation and functional characterization of peptide agonists of PTPRJ, a tyrosine phosphatase receptor endowed with tumor suppressor activityFrancesco Paduano, Francesco Ortuso, Pietro Campiglia, et al.Pageof 13