27 results on '"Bergé, Gilbert"'
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2. The novel nonapeptide acein targets angiotensin converting enzyme in the brain and induces dopamine release
3. Involvement of tryptophan W276 and of two surrounding amino acid residues in the high constitutive activity of the ghrelin receptor GHS-R1a
4. Solid-phase synthesis of dipeptidic and pseudo-dipeptidic potential NOS inhibitors through a side-chain anchoring approach
5. Synthesis and biological activities of peptidomimetic analogues of compound A71623, a potent and selective CCK-A receptor agonist
6. Solid phase synthesis of dipeptides and dipeptidomimetics substrate-based NOS inhibitors through a side-chain anchoring approach
7. A side-chain anchoring approach for the solid phase synthesis of dipeptides and dipeptidomimetics substrate-based NOS inhibitors
8. Solid phase synthesis of arginine derivatives : cyclic peptides with a guaninidine bridge and NOS inhibitors using a side-chai anchoring approach
9. Replacement of the alpha-aminoisobutyyl Moiety to obtain Potent Ghrelin Receptor 1,2,4-triazole Based Ligands
10. Solid phase synthesis of dipeptides and pseudo-dipeptides potential NOS inhibitors
11. Synthèse en phase solide d'inhibiteurs pseudo-peptidiques de NO Synthases
12. New series of Ghrelin Receptor Ligands : Structure Activity Relationship Study on the triazole Moiety
13. Design of Ghrelin Receptor Ligands : From Peptides to Peptidomimetics
14. Solid phase synthesis of dipeptidomimetic substrate-based NOS inhibitors through a side-chain anchoring approach
15. Design, synthesis, and biological evaluation of 1,5-benzothiazepine-4-one derivatives targeting factor VIIa/tissue factor
16. 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)
17. New Trisubstituted 1,2,4-Triazole Derivatives as Potent Ghrelin Receptor Antagonists. 3. Synthesis and Pharmacological in Vitro and in Vivo Evaluations
18. Toward Potent Ghrelin Receptor Ligands Based on Trisubstituted 1,2,4-Triazole Structure. 2. Synthesis and Pharmacological in Vitro and in Vivo Evaluations
19. Synthesis and Pharmacological in Vitro and in Vivo Evaluations of Novel Triazole Derivatives as Ligands of the Ghrelin Receptor. 1
20. Molecular modeling study for a novel structured oligomer subunit selection: the example of 2-aminomethyl-phenyl-acetic acid
21. On-Line Synthesis of Pseudopeptide Library Incorporating a Benzodiazepinone Turn Mimic: Biological Evaluation on MC1 Receptors
22. 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
23. Design and Synthesis of Potent Bradykinin Agonists Containing a Benzothiazepine Moiety
24. Synthesis and Characterization of Bradykinin B2 Receptor Agonists Containing Constrained Dipeptide Mimics
25. CholecystokininBReceptor from Human Jurkat Lymphoblastic T Cells Is Involved in Activator Protein-1-Responsive Gene Activation
26. Physicochemical and Structural Study of Sulfamethazine
27. On-line synthesis of pseudopeptide library incorporating a benzodiazepinone turn mimic: biological evaluation on MC1 receptors.
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