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Salvadori S.
Salvadori Severo
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http://hub.abes.fr/springer/periodical/726/1994/volume_7/issue_3/B941F28548CF3E94E053120B220AFD2A/authorship/1
http://hub.abes.fr/springer/periodical/259/1995/volume_22/issue_9/B8E924402C553944E053120B220A7E9F/authorship/4
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Chemotactic response of human monocytes to pentapeptide analog derived from immunodeficiency virus protein gp 120
Preparation of mono-radioiodinated tracers for study of the in vivo metabolism of atrial natriuretic peptide in humans
Phe3-substituted analogs of deltorphin C. Spatial conformation and topography of the aromatic ring in peptide recognition by .delta. opioid receptors
Simultaneous targeting of multiple opioid receptors: a strategy to improve side-effect profile
Evaluation of the Dmt−Tic Pharmacophore: Conversion of a Potent δ-OpioidReceptor Antagonist into a Potent δ Agonist and Ligands with MixedProperties
Unique High-Affinity Synthetic μ-Opioid Receptor Agonists with Central- andSystemic-Mediated Analgesia
Crystal Structures of Dipeptides Containing the Dmt-Tic Pharmacophore
Activation of DOR Attenuates Anoxic K+ Derangement via Inhibition of Na+ Entry in Mouse Cortex
Evolution of the Dmt-Tic Pharmacophore: N-Terminal Methylated Derivativeswith Extraordinary δ Opioid Antagonist Activity
Conversion of the Potent δ-OpioidAgonist H-Dmt-Tic-NH-CH2-Bid intoδ-Opioid Antagonists byN-Benzimidazole Alkylation1
Further Studies on Lead Compounds Containing the Opioid Pharmacophore Dmt-Tic
Synthesis of a Potent and Selective 18F-Labeled δ-Opioid Receptor Antagonist Derived from the Dmt-Tic Pharmacophore for Positron Emission Tomography Imaging
Synthesis and Pharmacological Activity of Deltorphin and Dermorphin-RelatedGlycopeptides
Structure−Activity Study of the Nociceptin(1−13)-NH2 N-Terminal Tetrapeptideand Discovery of a Nociceptin Receptor Antagonist
Potent δ-Opioid Receptor Agonists Containing the Dmt−Tic Pharmacophore
Direct Influence of C-Terminally Substituted Amino Acids in the Dmt−TicPharmacophore on δ-Opioid Receptor Selectivity and Antagonism
Highly Selective Fluorescent Analogue of the Potent δ-Opioid ReceptorAntagonist Dmt-Tic
New Opioid Designed Multiple Ligand from Dmt-Tic and Morphinan Pharmacophores
New 2‘,6‘-Dimethyl-l-tyrosine (Dmt) Opioid Peptidomimetics Based on the Aba-Gly Scaffold.Development of Unique μ-Opioid Receptor Ligands
Synthesis and Biological Activity of Human Neuropeptide S Analogues Modified in Position 2
6-N,N-Dimethylamino-2,3-naphthalimide: A New Environment-Sensitive Fluorescent Probe inδ- and μ-Selective Opioid Peptides
Effect of Lysine at C-Terminus of the Dmt-Tic Opioid Pharmacophore
Helix-Inducing α-Aminoisobutyric Acid in Opioid Mimetic Deltorphin CAnalogues
Further Studies on the Dmt-Tic Pharmacophore: Hydrophobic Substituents atthe C-Terminus Endow δ Antagonists To Manifest μ Agonism or μ Antagonism
Solution Structure of Amyloid β-Peptide (25−35) in Different Media
Triazine Compounds as Antagonists at Bv8-Prokineticin Receptors
Design and Synthesis of 1-Aminocycloalkane-1-carboxylic Acid-SubstitutedDeltorphin Analogues: Unique δ and μ Opioid Activity in Modified Peptides
Further Studies on Nociceptin-Related Peptides: Discovery of a New ChemicalTemplate with Antagonist Activity on the Nociceptin Receptor
Structure−Activity Studies of the Phe4 Residue of Nociceptin(1−13)-NH2: Identification of Highly Potent Agonists of the Nociceptin/Orphanin FQReceptor
Conformation−Activity Relationship of Neuropeptide S and Some Structural Mutants: HelicityAffects Their Interaction with the Receptor
Prerequisite for His4 in deltorphin A for highδ opioid receptor selectivity
Topographical conformations of the deltorphins predicate .delta. opioid receptor affinity
Stereospecificity of amino acid side chains in deltorphin defines binding to opioid receptors
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