The Novel Analogue of Modafinil CE-158 Protects Social Memory against Interference and Triggers the Release of Dopamine in the Nucleus Accumbens of Mice von Ebner, Karl, Sartori, Simone B, Murau, Rita, Kopel, Fabian, Kalaba, Predrag, Dragačević, Vladimir, Leban, Johann J, Singewald, Nicolas, Engelmann, Mario, Lubec, Gert

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A Novel Heterocyclic Compound CE-104 Enhances Spatial Working Memory in the Radial Arm Maze in Rats and Modulates the Dopaminergic System von Aher, Yogesh D, Subramaniyan, Saraswathi, Shanmugasundaram, Bharanidharan, Sase, Ajinkya, Saroja, Sivaprakasam R, Holy, Marion, Höger, Harald, Beryozkina, Tetyana, Sitte, Harald H, Leban, Johann J, Lubec, Gert

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Protein farnesyltransferase: kinetics of farnesyl pyrophosphate binding and product release von Furfine, Eric S, Leban, Johann J, Landavazo, Anthony, Moomaw, John F, Casey, Patrick J

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Base-Induced Dimerization of Urethane-Protected Amino Acid N-Carboxanhydrides von Leban, Johann J, Colson, Kimberly L

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Novel Modified Carboxy Terminal Fragments of Neuropeptide Y with High Affinity for Y2-Type Receptors and Potent Functional Antagonism at the Y1-Type Receptor von Leban, Johann J, Heyer, Dennis, Landavazo, Antonio, Matthews, Jessica, Aulabaugh, Ann, Daniels, Alejandro J

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Two-step binding mechanism for HIV protease inhibitors von Furfine, Eric S, D'Souza, Eric, Ingold, Kenneth J, Leban, Johann J, Spector, Thomas, Porter, David J. T

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High-Affinity Neuropeptide Y Receptor Antagonists von Daniels, Alejandro J., Matthews, Jessica E., Slepetis, Ruta J., Jansen, Marilyn, Viveros, O. Humberto, Tadepalli, Anjaneyulu, Harrington, Wallace, Heyer, Dennis, Landavazo, Antonio, Leban, Johann J., Spaltenstein, Andrew

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Hemodynamic Characterization of a Novel Neuropeptide Y Receptor Antagonist von Tadepalli, Anjaneyulu S, Harrington, W Wallace, Hashim, Mir A, Matthews, Jessica, Leban, Johann J, Spaltenstein, Andrew, Daniels, Alejandro J

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Potent Gastrin-Releasing Peptide (GRP) Antagonists Derived from GRP(19-27) with a C-Terminal DPro.PSI.[CH2NH]Phe-NH2 and N-Terminal Aromatic Residues von Leban, Johann J, Landavazo, Antonio, McDermed, John D, Diliberto, Emanuel J, Jansen, Marilyn, Stockstill, Beth, Kull, Frederick C

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Synthesis, structure and stability of novel dimeric peptide-disulfides von LEBAN, JOHANN J., SPALTENSTEIN, ANDREW, LANDAVAZO, ANTONIO, CHESTNUT, WILLIAM, AULABAUGH, ANN, TAYLOR, LESTER C.E., DANIELS, ALEJANDRO J.

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Design and synthesis of novel protease inhibitors. Tripeptide α′,β′-epoxyketones as nanomolar inactivators of the proteasome von Spaltenstein, Andrew, Leban, Johann J., Huang, Jim J., Reinhardt, Kelli R., Humberto Viveros, O., Sigafoos, Jim, Crouch, Ronald

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Development of potent gastrin-releasing peptide antagonists having a D-Pro-psi(CH2NH)-Phe-NH2 C terminus von J J Leban, F C Kull, Jr, A Landavazo, B Stockstill, J D McDermed

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BW2258U89: A GRP receptor antagonist which inhibits small cell lung cancer growth von Moody, Terry W., Venugopal, Rajesh, Zia, Farah, Patierno, Steven, Leban, Johann J., McDermed, John

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Structure-activity relationship of novel pentapeptide neuropeptide Y receptor antagonists is consistent with a noncontinuous epitope for ligand-receptor binding von Daniels, A J, Matthews, J E, Viveros, O H, Leban, J J, Cory, M, Heyer, D

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Synthesis of C2-symmetric HIV-protease inhibitors with sulfur-containing central units von SPALTENSTEIN, A, LEBAN, J. J, FURFINE, E. S

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Conveyance of partial agonism/antagonism to bombesin/gastrin-releasing peptide analogues on Swiss 3T3 cells by a carboxyl-terminal leucine insertion von F C Kull, Jr, J J Leban, A Landavazo, K D Stewart, B Stockstill, J D McDermed

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Potent gastrin-releasing peptide (GRP) antagonists derived from GRP (19-27) with a C-terminal DPro psi [CH2NH]Phe-NH2 and N-terminal aromatic residues von Leban, J J, Landavazo, A, McDermed, J D, Diliberto, Jr, E J, Jansen, M, Stockstill, B, Kull, Jr, F C

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Synthesis of C 2-symmetric HIV-protease inhibitors with sulfur-containing central units von Spaltenstein, Andrew, Leban, Johann J., Furfine, Eric S.

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A novel bombesin receptor antagonist (2258U89), potently inhibits bombesin evoked release of gastrointestinal hormones from rats and dogs, in vitro and in vivo von Singh, Pomila, Guo, Yan-Shi, Kull, Frederick C., Leban, Johann J.

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Development of Potent Gastrin-Releasing Peptide Antagonists Having a D-Pro- Ψ(CH2NH)-Phe-NH2C Terminus von Leban, Johann J., Kull, Frederick C., Landavazo, Antonio, Stockstill, Beth, McDermed, John D.

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