John M. Gerdes

Novel Lavendamycin Analogues as Antitumor Agents:  Synthesis, in Vitro Cytotoxicity, Structure−Metabolism, and Computational Molecular Modeling Studies with NAD(P)H:Quinone Oxidoreductase 1

Mary Hassani, Wen Cai, David C. Holley et al. · Journal of Medicinal Chemistry · 2005 · 75 citations

The substituted aspartate analogue l-β-threo-benzyl-aspartate preferentially inhibits the neuronal excitatory amino acid transporter EAAT3

C. Sean Esslinger, Shailesh R. Agarwal, John M. Gerdes et al. · Neuropharmacology · 2005 · 57 citations

Synaptic Plasticity, Molecular Neuroscience, Transporter Eaat3 +12

Organic reactions at high pressure. The preparative scale synthesis of cantharidin

William G. Dauben, John M. Gerdes, David B. Smith · The Journal of Organic Chemistry · 1985 · 44 citations

Organic Reactions, Engineering, Chemical Analysis +12

Lavendamycin Antitumor Agents: Structure-Based Design, Synthesis, and NAD(P)H:Quinone Oxidoreductase 1 (NQO1) Model Validation with Molecular Docking and Biological Studies

Mary Hassani, Wen Cai, Katherine H. Koelsch et al. · Journal of Medicinal Chemistry · 2008 · 43 citations

Synthesis and in vitro evaluation of 2,3-dimethoxy-5-(fluoroalkyl)-substituted benzamides: high-affinity ligands for CNS dopamine D2 receptors

John E. Bishop, Chester A. Mathis, John M. Gerdes et al. · Journal of Medicinal Chemistry · 1991 · 42 citations · Full text