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Chemmedchem|July 9, 2013
Chemical, pharmacological, and in vitro metabolic stability studies on enantiomerically pure RC-33 compounds: promising neuroprotective agents acting as σ₁ receptor agonistsDaniela Rossi, Alice Pedrali, Raffaella Gaggeri, et al.
Chemmedchem|December 5, 2012
Thiadiazole-a promising structure in medicinal chemistryYijing Li, Jingkun Geng, Yang Liu, et al.
Chemmedchem|December 11, 2012
2-Phenoxy-nicotinamides are potent agonists at the bile acid receptor GPBAR1 (TGR5)Rainer E Martin, Caterina Bissantz, Olivier Gavelle, et al.
Chemmedchem|April 26, 2012
Kinase inhibitor scaffolds against neurodegenerative diseases from a Southern Australian ascidian, Didemnum spFabien Plisson, Melissa Conte, Zeinab Khalil, et al.
Chemmedchem|May 15, 2012
Discovery of 3H-imidazo[4,5-b]pyridines as potent c-Met kinase inhibitors: design, synthesis, and biological evaluationDanqi Chen, Ying Wang, Yuchi Ma, et al.
Chemmedchem|December 4, 2012
Identification of LasR ligands through a virtual screening approachSøren Skovstrup, Sebastian Thordal Le Quement, Thomas Hansen, et al.
Chemmedchem|November 28, 2012
Highly ligand efficient and selective N-2-(Thioethyl)picolinamide histone deacetylase inhibitors inspired by the natural product psammaplin AMatthias G J Baud, Patricia Haus, Thomas Leiser, et al.
Chemmedchem|November 29, 2013
Inhibition of hypoxia-induced gene transcription by substituted pyrazolyl oxadiazoles: initial lead generation and structure-activity relationshipsMichael Härter, Karl-Heinz Thierauch, Stephen Boyer, et al.
Chemmedchem|November 29, 2013
Discovery of potent HDAC inhibitors based on chlamydocin with inhibitory effects on cell migrationShimiao Wang, Xiaohui Li, Yingdong Wei, et al.
Chemmedchem|November 26, 2013
Discovery of 7-aryl-substituted (1,5-naphthyridin-4-yl)ureas as aurora kinase inhibitorsJulien Defaux, Maud Antoine, Marc Le Borgne, et al.
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