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The Novel Analogue of Modafinil CE-158 Protects Social Memory against Interference and Triggers the Release of Dopamine in the Nucleus Accumbens of Mice

Biomolecules (Basel, Switzerland), 2022-03, Vol.12 (4), p.506

2022

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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

Frontiers in behavioral neuroscience, 2016-02, Vol.10, p.20-20

2016

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Protein farnesyltransferase: kinetics of farnesyl pyrophosphate binding and product release

Biochemistry (Easton), 1995-05, Vol.34 (20), p.6857-6862

1995

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Base-Induced Dimerization of Urethane-Protected Amino Acid N-Carboxanhydrides

Journal of organic chemistry, 1996-01, Vol.61 (1), p.228-231

1996

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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

Journal of medicinal chemistry, 1995-03, Vol.38 (7), p.1150-1157

1995

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Two-step binding mechanism for HIV protease inhibitors

Biochemistry (Easton), 1992-09, Vol.31 (34), p.7886-7891

1992

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High-Affinity Neuropeptide Y Receptor Antagonists

Proceedings of the National Academy of Sciences - PNAS, 1995-09, Vol.92 (20), p.9067-9071

1995

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Hemodynamic Characterization of a Novel Neuropeptide Y Receptor Antagonist

Journal of cardiovascular pharmacology, 1996-05, Vol.27 (5), p.712-718

1996

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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

Journal of medicinal chemistry, 1994-02, Vol.37 (4), p.439-445

1994

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Synthesis, structure and stability of novel dimeric peptide-disulfides

International Journal of Peptide and Protein Research, 1996-03, Vol.47 (3), p.161-166

1996

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Design and synthesis of novel protease inhibitors. Tripeptide α′,β′-epoxyketones as nanomolar inactivators of the proteasome

Tetrahedron letters, 1996-01, Vol.37 (9), p.1343-1346

1996

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Development of potent gastrin-releasing peptide antagonists having a D-Pro-psi(CH2NH)-Phe-NH2 C terminus

Proceedings of the National Academy of Sciences - PNAS, 1993-03, Vol.90 (5), p.1922-1926

1993

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BW2258U89: A GRP receptor antagonist which inhibits small cell lung cancer growth

Life sciences (1973), 1995, Vol.56 (7), p.521-529

1995

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Structure-activity relationship of novel pentapeptide neuropeptide Y receptor antagonists is consistent with a noncontinuous epitope for ligand-receptor binding

Molecular pharmacology, 1995-09, Vol.48 (3), p.425-432

1995

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Synthesis of C2-symmetric HIV-protease inhibitors with sulfur-containing central units

Tetrahedron letters, 1993-02, Vol.34 (9), p.1457-1460

1993

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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

The Journal of biological chemistry, 1992-10, Vol.267 (29), p.21132-21138

1992

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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

Journal of medicinal chemistry, 1994-02, Vol.37 (4), p.439

1994

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Synthesis of C 2-symmetric HIV-protease inhibitors with sulfur-containing central units

Tetrahedron letters, 1993, Vol.34 (9), p.1457-1460

1993

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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

Regulatory peptides, 1992-07, Vol.40 (1), p.75-86

1992

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Development of potent gastrin-releasing peptide antagonists having a D-Pro-(Psi)(CH(2)NH)-Phe-NH(2) C terminus

Proceedings of the National Academy of Sciences - PNAS, 1993-03, Vol.90 (5), p.1922

1993

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Development of Potent Gastrin-Releasing Peptide Antagonists Having a D-Pro- Ψ(CH2NH)-Phe-NH2C Terminus

Proceedings of the National Academy of Sciences - PNAS, 1993-03, Vol.90 (5), p.1922-1926

1993

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Synthesis of Peptides Related to Substance P and Their Activities as Agonists and Antagonists

Acta chemica Scandinavica (Copenhagen. 1989), 1979, Vol.33b, p.375-378

1979

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Synthesis and Biological Activity of Analogs of Substance P, Modified for Conformational Information by D-Amino Acids

Acta chemica Scandinavica (Copenhagen. 1989), 1979, Vol.33b, p.63-68

1979

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Dependence of Equilibrium Geometry and Rearrangement Modes on Electron Count in One Class of Trinuclear Complexes of Acetylene

Acta chemica Scandinavica (Copenhagen. 1989), 1979, Vol.33b, p.231-232

1979

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Sulfonation of 2- and 3-Methylphenol

Acta chemica Scandinavica (Copenhagen. 1989), 1979, Vol.33b, p.261-264

1979

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The Novel Analogue of Modafinil CE-158 Protects Social Memory against Interference and Triggers the Release of Dopamine in the Nucleus Accumbens of Mice

A Novel Heterocyclic Compound CE-104 Enhances Spatial Working Memory in the Radial Arm Maze in Rats and Modulates the Dopaminergic System

Protein farnesyltransferase: kinetics of farnesyl pyrophosphate binding and product release

Base-Induced Dimerization of Urethane-Protected Amino Acid N-Carboxanhydrides

Novel Modified Carboxy Terminal Fragments of Neuropeptide Y with High Affinity for Y2-Type Receptors and Potent Functional Antagonism at the Y1-Type Receptor

Two-step binding mechanism for HIV protease inhibitors

High-Affinity Neuropeptide Y Receptor Antagonists

Hemodynamic Characterization of a Novel Neuropeptide Y Receptor Antagonist

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

Synthesis, structure and stability of novel dimeric peptide-disulfides

Design and synthesis of novel protease inhibitors. Tripeptide α′,β′-epoxyketones as nanomolar inactivators of the proteasome

Development of potent gastrin-releasing peptide antagonists having a D-Pro-psi(CH2NH)-Phe-NH2 C terminus

BW2258U89: A GRP receptor antagonist which inhibits small cell lung cancer growth

Structure-activity relationship of novel pentapeptide neuropeptide Y receptor antagonists is consistent with a noncontinuous epitope for ligand-receptor binding

Synthesis of C2-symmetric HIV-protease inhibitors with sulfur-containing central units

Conveyance of partial agonism/antagonism to bombesin/gastrin-releasing peptide analogues on Swiss 3T3 cells by a carboxyl-terminal leucine insertion

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

Synthesis of C 2-symmetric HIV-protease inhibitors with sulfur-containing central units

A novel bombesin receptor antagonist (2258U89), potently inhibits bombesin evoked release of gastrointestinal hormones from rats and dogs, in vitro and in vivo

Development of potent gastrin-releasing peptide antagonists having a D-Pro-(Psi)(CH(2)NH)-Phe-NH(2) C terminus

Development of Potent Gastrin-Releasing Peptide Antagonists Having a D-Pro- Ψ(CH2NH)-Phe-NH2C Terminus

Synthesis of Peptides Related to Substance P and Their Activities as Agonists and Antagonists

Synthesis and Biological Activity of Analogs of Substance P, Modified for Conformational Information by D-Amino Acids

Dependence of Equilibrium Geometry and Rearrangement Modes on Electron Count in One Class of Trinuclear Complexes of Acetylene

Sulfonation of 2- and 3-Methylphenol

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