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Chemmedchem|December 26, 2019
A Flexible Strategy for Modular Synthesis of Curcuminoid-BF2 /Curcuminoid Pairs and Their Comparative Antiproliferative Activity in Human Cancer Cell LinesRodrigo Abonia, Kenneth K Laali, Dawn Raja Somu, et al.Chemmedchem|December 19, 2019
Targeting iNOS As a Valuable Strategy for the Therapy of GliomaCristina Maccallini, Marialucia Gallorini, Amelia Cataldi, et al.Chemmedchem|August 29, 2020
4,4,16-Trifluoropalmitate: Design, Synthesis, Tritiation, Radiofluorination and Preclinical PET Imaging Studies on Myocardial Fatty Acid OxidationAlessandro Colombano, Sergio Dall'Angelo, Lee Kingston, et al.Chemmedchem|October 29, 2019
Trifluoromethyl Dihydrothiazine-Based β-Secretase (BACE1) Inhibitors with Robust Central β-Amyloid Reduction and Minimal Covalent Binding BurdenKosuke Anan, Yasuyoshi Iso, Takuya Oguma, et al.Chemmedchem|October 27, 2020
Small-Molecule Inhibition of the uPAR ⋅ uPA Interaction by Conformational SelectionDavid Xu, Khuchtumur Bum-Erdene, Julie M Leth, et al.Chemmedchem|October 29, 2020
50 Years European Federation for Medicinal Chemistry (EFMC) - The Ascent of Medicinal Chemistry in EuropeEdmond DifferdingChemmedchem|October 10, 2020
A Comprehensive Overview of Structure-Activity Relationships of Small-Molecule Splicing Modulators Targeting SF3B1 as Anticancer AgentsDatong Zhang, Fancui MengChemmedchem|October 8, 2020
Two Methods, One Goal: Structural Differences between Cocrystallization and Crystal Soaking to Discover Ligand Binding PosesBarbara Wienen-Schmidt, Matthias Oebbeke, Khang Ngo, et al.Chemmedchem|July 31, 2021
Rational Design of Potent Inhibitors of a Metallohydrolase Using a Fragment-Based ApproachDaniel Feder, Siti H Mohd-Pahmi, Waleed M Hussein, et al.Chemmedchem|July 9, 2021
MPI8 is Potent against SARS-CoV-2 by Inhibiting Dually and Selectively the SARS-CoV-2 Main Protease and the Host Cathepsin LXinyu R Ma, Yugendar R Alugubelli, Yuying Ma, et al.Pageof 460