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Chemmedchem|May 3, 2021
Cyclic Dipeptide: A Privileged Molecular Scaffold to Derive Structural Diversity and Functional UtilityChenikkayala Balachandra, Dikshaa Padhi, Thimmaiah Govindaraju
Chemmedchem|February 27, 2023
Discovery of Antitrypanosomal Indolylacetamides by a Deconstruction-Optimization Strategy Applied to PaullonesJens C Lindhof, Irina Ihnatenko, Marco J Müller, et al.
Chemmedchem|February 28, 2023
Facile, Single-Step Synthesis of a Series of D-Ring Ethisterones Substituted with 1,4-1,2,3-Triazoles: Preliminary Evaluation of Cytotoxic ActivitiesDaniel Canseco-González, Isaac Rodríguez-Victoria, Teresa Apan-Ramírez, et al.
Chemmedchem|August 17, 2021
FOXM1 Inhibitors as Potential Diagnostic Agents: First Generation of a PET Probe Targeting FOXM1 To Detect Triple-Negative Breast Cancer in vitro and in vivoDavid J Pérez, Seyed Amirhossein Tabatabaei Dakhili, Cody Bergman, et al.
Chemmedchem|August 20, 2021
Mutual Prodrugs of 5-Fluorouracil: From a Classic Chemotherapeutic Agent to Novel Potential Anticancer DrugsValeria Ciaffaglione, Maria N Modica, Valeria Pittalà, et al.
Chemmedchem|August 18, 2022
Synthesis, Biological Evaluation, and Binding Mode of a New Class of Oncogenic K-Ras4b InhibitorsStephan Jeuken, Oleksandr Shkura, Marc Röger, et al.
Chemmedchem|November 9, 2022
Prodrugs of the Archetypal Dynamin Inhibitor Bis-T-22Luke R Odell, Mark J Robertson, Kelly A Young, et al.
Chemmedchem|December 8, 2025
Design, Synthesis, and Evaluation of Novel Inhibitors of Aminoglycoside-Resistance 16S Ribosomal RNA MethyltransferasesBenjamin E Deprez, Debayan Dey, Natalia Zelinskaya, et al.
Chemmedchem|November 30, 2025
Small-Molecule Sarco/Endoplasmic Reticulum Ca2+-ATPase Activators Reverse Methylglyoxal-Induced Inhibition through Nonantioxidant MechanismsCarlos Cruz-Cortés, Silvia Micháliková, Petronela Rezbáriková, et al.
Chemmedchem|December 21, 2025
Investigating the Ligand-Binding Properties of N-arylbenzimidazoles as Novel Elastase InhibitorsGiovanna Pitasi, Sonia Floris, Francesca Mancuso, et al.
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