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Chemistry & Biology|June 26, 2004
Structure-activity relationships in purine-based inhibitor binding to HSP90 isoformsLisa Wright, Xavier Barril, Brian Dymock, et al.The Journal of Biological Chemistry|June 15, 2014
Mechanistic insight into the enzymatic reduction of truncated hemoglobin N of Mycobacterium tuberculosis: role of the CD loop and pre-A motif in electron cyclingSandeep Singh, Naveen Thakur, Ana Oliveira, et al.Journal of Medicinal Chemistry|August 29, 2025
N-[(Thiophen-3-yl)methyl]benzamides as Fusion Inhibitors of Influenza Virus Targeting H1 and H5 HemagglutininsSilke Rimaux, Aitor Valdivia, Juan Martín-López, et al.European Journal of Medicinal Chemistry|February 7, 2018
First homology model of Plasmodium falciparum glucose-6-phosphate dehydrogenase: Discovery of selective substrate analog-based inhibitors as novel antimalarial agentsNelson Alencar, Irene Sola, María Linares, et al.European Journal of Medicinal Chemistry|May 24, 2017
Novel propanamides as fatty acid amide hydrolase inhibitorsAlessandro Deplano, Carmine Marco Morgillo, Monica Demurtas, et al.Molecules (Basel, Switzerland)|May 6, 2017
Breakthroughs in Medicinal Chemistry: New Targets and Mechanisms, New Drugs, New HopesDiego Muñoz-Torrero, Arduino A Mangoni, Catherine Guillou, et al.Computational and Structural Biotechnology Journal|September 11, 2020
Structural and functional properties of Antarctic fish cytoglobins-1: Cold-reactivity in multi-ligand reactionsDaniela Giordano, Alessandra Pesce, Stijn Vermeylen, et al.Angewandte Chemie (International Ed. in English)|June 18, 2016
Insertion of Isocyanides into N-Si Bonds: Multicomponent Reactions with Azines Leading to Potent Antiparasitic CompoundsKranti G Kishore, Ouldouz Ghashghaei, Carolina Estarellas, et al.Chemmedchem|April 8, 2009
Synthesis, structural analysis, and biological evaluation of thioxoquinazoline derivatives as phosphodiesterase 7 inhibitorsTania Castaño, Huanchen Wang, Nuria E Campillo, et al.Journal of Medicinal Chemistry|February 27, 2014
Synthesis and multitarget biological profiling of a novel family of rhein derivatives as disease-modifying anti-Alzheimer agentsElisabet Viayna, Irene Sola, Manuela Bartolini, et al.Pageof 28