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Toward Potent Ghrelin Receptor Ligands Based on Trisubstituted 1,2,4-Triazole Structure. 2. Synthesis and Pharmacological in Vitro and in Vivo Evaluations

Journal of medicinal chemistry, 2007-11, Vol.50 (23), p.5790-5806

2007

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New Trisubstituted 1,2,4-Triazole Derivatives as Potent Ghrelin Receptor Antagonists. 3. Synthesis and Pharmacological in Vitro and in Vivo Evaluations

Journal of medicinal chemistry, 2008-02, Vol.51 (3), p.689-693

2008

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Synthesis and Pharmacological in Vitro and in Vivo Evaluations of Novel Triazole Derivatives as Ligands of the Ghrelin Receptor. 1

Journal of medicinal chemistry, 2007-04, Vol.50 (8), p.1939-1957

2007

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The novel nonapeptide acein targets angiotensin converting enzyme in the brain and induces dopamine release

British journal of pharmacology, 2016-04, Vol.173 (8), p.1314-1328

2016

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Activation of the Ghrelin Receptor is Described by a Privileged Collective Motion: A Model for Constitutive and Agonist-induced Activation of a Sub-class A G-Protein Coupled Receptor (GPCR)

Journal of molecular biology, 2010-01, Vol.395 (4), p.769-784

2010

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Involvement of tryptophan W276 and of two surrounding amino acid residues in the high constitutive activity of the ghrelin receptor GHS-R1a

European journal of pharmacology, 2010-09, Vol.643 (2), p.153-161

2010

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Molecular modeling study for a novel structured oligomer subunit selection: the example of 2-aminomethyl-phenyl-acetic acid

Tetrahedron letters, 2007-03, Vol.48 (10), p.1787-1790

2007

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Design, synthesis, and biological evaluation of 1,5-benzothiazepine-4-one derivatives targeting factor VIIa/tissue factor

Bioorganic & medicinal chemistry letters, 2009-03, Vol.19 (5), p.1386-1391

2009

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Cross-interactions of Two p38 Mitogen-activated Protein (MAP) Kinase Inhibitors and Two Cholecystokinin (CCK) Receptor Antagonists with the CCK1 Receptor and P38 MAP Kinase

The Journal of biological chemistry, 2005-06, Vol.280 (22), p.21384-21393

2005

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Solid-phase synthesis of dipeptidic and pseudo-dipeptidic potential NOS inhibitors through a side-chain anchoring approach

Advances in experimental medicine and biology, 2009, Vol.611, p.133-134

2009

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Involvement of tryptophan W276 and of two surrounding amino acid residues in the high constitutive activity of the ghrelin receptor GHS-R1 a

European journal of pharmacology, 2010, Vol.643 (2-3), p.153-161

2010

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On-Line Synthesis of Pseudopeptide Library Incorporating a Benzodiazepinone Turn Mimic: Biological Evaluation on MC1 Receptors

Journal of combinatorial chemistry, 2007-03, Vol.9 (2), p.254-262

2007

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Design and Synthesis of Potent Bradykinin Agonists Containing a Benzothiazepine Moiety

Journal of medicinal chemistry, 1999-10, Vol.42 (20), p.4185-4192

1999

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Synthesis and Characterization of Bradykinin B 2 Receptor Agonists Containing Constrained Dipeptide Mimics

Journal of medicinal chemistry, 1999-10, Vol.42 (20), p.4193-4201

1999

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Synthesis and Characterization of Bradykinin B2 Receptor Agonists Containing Constrained Dipeptide Mimics

Journal of medicinal chemistry, 1999-10, Vol.42 (20), p.4193-4201

1999

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Physicochemical and Structural Study of Sulfamethazine

Journal of pharmaceutical sciences, 1985-04, Vol.74 (4), p.422-426

1985

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Correction to: “Physicochemical and Structural Study ofSulfamethazine”

Journal of pharmaceutical sciences, 1985-12, Vol.74 (12), p.1344-1344

1985

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Syntheses and biological activities of bombesin analogs modified in the C-terminal dipeptide part

European journal of medicinal chemistry, 1997, Vol.32 (10), p.767-780

1997

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Études électrocapillaires : solution de fluorure de sodium

Journal de chimie physique et de physicochimie biologique, 1970, Vol.67, p.1671-1673

1970

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L’inhibition d’une réduction électrochimique par des ammoniums quaternaires

Journal de chimie physique et de physicochimie biologique, 1972, Vol.69, p.306-310

1972

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Cholecystokinin B Receptor from Human Jurkat Lymphoblastic T Cells Is Involved in Activator Protein-1-Responsive Gene Activation

Molecular pharmacology, 1997-08, Vol.52 (2), p.292-299

1997

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Synthesis and biological activities of peptidomimetic analogues of compound A71623, a potent and selective CCK-A receptor agonist

Letters in Peptide Science, 1997, Vol.4 (4-6), p.235-239

1997

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Absent CNKSR2 causes seizures and intellectual, attention, and language deficits

Annals of neurology, 2014-11, Vol.76 (5), p.758-764

2014

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Koronavaksinasjon: Frykt for sprøyter kan dempes med enkle tiltak

Sykepleien forskning (Oslo), 2021 (83420), p.e-83420

2021

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Science-policy challenges for biodiversity, public health and urbanization: examples from Belgium

Environmental research letters, 2013-06, Vol.8 (2), p.1-19

2013

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Toward Potent Ghrelin Receptor Ligands Based on Trisubstituted 1,2,4-Triazole Structure. 2. Synthesis and Pharmacological in Vitro and in Vivo Evaluations

New Trisubstituted 1,2,4-Triazole Derivatives as Potent Ghrelin Receptor Antagonists. 3. Synthesis and Pharmacological in Vitro and in Vivo Evaluations

Synthesis and Pharmacological in Vitro and in Vivo Evaluations of Novel Triazole Derivatives as Ligands of the Ghrelin Receptor. 1

The novel nonapeptide acein targets angiotensin converting enzyme in the brain and induces dopamine release

Activation of the Ghrelin Receptor is Described by a Privileged Collective Motion: A Model for Constitutive and Agonist-induced Activation of a Sub-class A G-Protein Coupled Receptor (GPCR)

Involvement of tryptophan W276 and of two surrounding amino acid residues in the high constitutive activity of the ghrelin receptor GHS-R1a

Molecular modeling study for a novel structured oligomer subunit selection: the example of 2-aminomethyl-phenyl-acetic acid

Design, synthesis, and biological evaluation of 1,5-benzothiazepine-4-one derivatives targeting factor VIIa/tissue factor

Cross-interactions of Two p38 Mitogen-activated Protein (MAP) Kinase Inhibitors and Two Cholecystokinin (CCK) Receptor Antagonists with the CCK1 Receptor and P38 MAP Kinase

Solid-phase synthesis of dipeptidic and pseudo-dipeptidic potential NOS inhibitors through a side-chain anchoring approach

Involvement of tryptophan W276 and of two surrounding amino acid residues in the high constitutive activity of the ghrelin receptor GHS-R1 a

On-Line Synthesis of Pseudopeptide Library Incorporating a Benzodiazepinone Turn Mimic: Biological Evaluation on MC1 Receptors

Design and Synthesis of Potent Bradykinin Agonists Containing a Benzothiazepine Moiety

Synthesis and Characterization of Bradykinin B 2 Receptor Agonists Containing Constrained Dipeptide Mimics

Synthesis and Characterization of Bradykinin B2 Receptor Agonists Containing Constrained Dipeptide Mimics

Physicochemical and Structural Study of Sulfamethazine

Correction to: “Physicochemical and Structural Study ofSulfamethazine”

Syntheses and biological activities of bombesin analogs modified in the C-terminal dipeptide part

Études électrocapillaires : solution de fluorure de sodium

L’inhibition d’une réduction électrochimique par des ammoniums quaternaires

Cholecystokinin B Receptor from Human Jurkat Lymphoblastic T Cells Is Involved in Activator Protein-1-Responsive Gene Activation

Synthesis and biological activities of peptidomimetic analogues of compound A71623, a potent and selective CCK-A receptor agonist

Absent CNKSR2 causes seizures and intellectual, attention, and language deficits

Koronavaksinasjon: Frykt for sprøyter kan dempes med enkle tiltak

Science-policy challenges for biodiversity, public health and urbanization: examples from Belgium

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