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Chemmedchem|October 6, 2011
Urolithin as a converging scaffold linking ellagic acid and coumarin analogues: design of potent protein kinase CK2 inhibitorsGiorgio Cozza, Alessandra Gianoncelli, Paolo Bonvini, et al.Chemmedchem|October 26, 2011
Development of improved PPARβ/δ inhibitorsPhilipp M Toth, Simone Naruhn, Veronika F S Pape, et al.Chemmedchem|December 20, 2014
"Squalenoylcurcumin" nanoassemblies as water-dispersible drug candidates with antileishmanial activityZakaria Cheikh-Ali, Joachim Caron, Sandrine Cojean, et al.Chemmedchem|December 4, 2014
Small-molecule inhibitors that target protein-protein interactions in the RAD51 family of recombinasesDuncan E Scott, Anthony G Coyne, Ashok Venkitaraman, et al.Chemmedchem|July 28, 2015
Synthesis and Antiplasmodial Activity of Novel Chloroquine Analogues with Bulky Basic Side ChainsBruno Tasso, Federica Novelli, Michele Tonelli, et al.Chemmedchem|February 19, 2016
Small-Molecule CD4 Mimics Containing Mono-cyclohexyl Moieties as HIV Entry InhibitorsNami Ohashi, Shigeyoshi Harada, Takaaki Mizuguchi, et al.Chemmedchem|December 9, 2015
Small-Molecule Stabilization of the 14-3-3/Gab2 Protein-Protein Interaction (PPI) InterfaceDavid Bier, Maria Bartel, Katharina Sies, et al.Chemmedchem|December 15, 2015
EPR Studies of V-ATPase with Spin-Labeled Inhibitors DCC and Archazolid: Interaction Dynamics with Proton Translocating Subunit cJan Philipp Gölz, Svenja Bockelmann, Kerstin Mayer, et al.Chemmedchem|December 5, 2015
Fighting Cancer with Transition Metal Complexes: From Naked DNA to Protein and Chromatin Targeting StrategiesGiulia Palermo, Alessandra Magistrato, Tina Riedel, et al.Chemmedchem|November 27, 2015
Inspired by Nature: The 3-Halo-4,5-dihydroisoxazole Moiety as a Novel Molecular Warhead for the Design of Covalent InhibitorsAndrea Pinto, Lucia Tamborini, Gregorio Cullia, et al.Pageof 469