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Chempluschem|January 22, 2020
Functionalization of Ruthenium(II)(η6 -p-cymene)(3-hydroxy-2-pyridone) Complexes with (Thio)Morpholine: Synthesis and Bioanalytical StudiesMuhammad Hanif, Samuel M Meier, Zenita Adhireksan, et al.Journal of Clinical Microbiology|August 8, 2006
Multicenter comparison of nucleic acid extraction methods for detection of severe acute respiratory syndrome coronavirus RNA in stool specimensA Petrich, J Mahony, S Chong, et al.Inorganic Chemistry|November 9, 2018
From Catalysis to Cancer: Toward Structure-Activity Relationships for Benzimidazol-2-ylidene-Derived N-Heterocyclic-Carbene Complexes as Anticancer AgentsNelson Y S Lam, Dianna Truong, Hilke Burmeister, et al.Journal of Medicinal Chemistry|December 19, 2017
Next-Generation Hypoxic Cell Radiosensitizers: Nitroimidazole AlkylsulfonamidesMuriel Bonnet, Cho Rong Hong, Way Wua Wong, et al.Journal of Medicinal Chemistry|September 19, 2019
Inhibition of the Cytolytic Protein Perforin Prevents Rejection of Transplanted Bone Marrow Stem Cells in VivoJulie A Spicer, Christian K Miller, Patrick D O'Connor, et al.ACS Pharmacology & Translational Science|June 17, 2022
Preclinical Activity and Pharmacokinetic/Pharmacodynamic Relationship for a Series of Novel Benzenesulfonamide Perforin InhibitorsKate H Gartlan, Jagdish K Jaiswal, Matthew R Bull, et al.Oncotarget|May 25, 2017
Biological characterization of SN32976, a selective inhibitor of PI3K and mTOR with preferential activity to PI3Kα, in comparison to established pan PI3K inhibitorsGordon W Rewcastle, Sharada Kolekar, Christina M Buchanan, et al.Journal of Food Protection|February 5, 2005
An international outbreak of salmonellosis associated with raw almonds contaminated with a rare phage type of Salmonella enteritidisS Isaacs, J Aramini, B Ciebin, et al.Journal of Medicinal Chemistry|September 3, 2011
Synthesis and biological evaluation of novel analogues of the pan class I phosphatidylinositol 3-kinase (PI3K) inhibitor 2-(difluoromethyl)-1-[4,6-di(4-morpholinyl)-1,3,5-triazin-2-yl]-1H-benzimidazole (ZSTK474)Gordon W Rewcastle, Swarna A Gamage, Jack U Flanagan, et al.Journal of Medicinal Chemistry|August 11, 2012
3-(3,4-Dihydroisoquinolin-2(1H)-ylsulfonyl)benzoic Acids: highly potent and selective inhibitors of the type 5 17-β-hydroxysteroid dehydrogenase AKR1C3Stephen M F Jamieson, Darby G Brooke, Daniel Heinrich, et al.Pageof 12