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Chemmedchem|December 29, 2007
Carbonic anhydrase inhibitors: binding of indanesulfonamides to the human isoform IIKatia D'Ambrosio, Bernard Masereel, Anne Thiry, et al.Chemmedchem|December 21, 2016
Metal NHC Complexes with Naphthalimide Ligands as DNA-Interacting Antiproliferative AgentsWojciech Streciwilk, Alessio Terenzi, Rainer Misgeld, et al.Chemmedchem|December 20, 2016
Phosphatase-Stable Phosphoamino Acid Mimetics That Enhance Binding Affinities with the Polo-Box Domain of Polo-like Kinase 1David Hymel, Terrence R BurkeChemmedchem|December 22, 2016
Intrinsic Thermodynamics and Structures of 2,4- and 3,4-Substituted Fluorinated Benzenesulfonamides Binding to Carbonic AnhydrasesAsta Zubrienė, Alexey Smirnov, Virginija Dudutienė, et al.Chemmedchem|January 10, 2017
Form Matters: Stable Helical Foldamers Preferentially Target Human Monocytes and GranulocytesBenedetta Del Secco, Giulia Malachin, Lorenzo Milli, et al.Chemmedchem|December 30, 2016
Discovery of Macrocyclic Pyrimidines as MerTK-Specific InhibitorsAndrew L McIver, Weihe Zhang, Qingyang Liu, et al.Chemmedchem|December 30, 2016
The Development of Next-Generation Pyridinium-Based multiQAC AntisepticsSaleh E Al-Khalifa, Megan C Jennings, William M Wuest, et al.Chemmedchem|April 15, 2014
Total synthesis of anticoagulant pentasaccharide fondaparinuxTiehai Li, Hui Ye, Xuefeng Cao, et al.Chemmedchem|April 15, 2014
Caulerpenyne and related bis-enol esters are novel-type inhibitors of human 5-lipoxygenasePhillipp Richter, Gregor Schubert, Anja Maria Schaible, et al.Chemmedchem|January 16, 2008
Taxane analogues against breast cancer: a quantitative structure-activity relationship studyRajeshwar P Verma, Corwin HanschPageof 459