12 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
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Article Title
Organization
Structure-activity relationship of imidazopyridinium analogues as antagonists of neuropeptide s receptor.
National Institutes of Health
Conformation-activity relationship of neuropeptide S and some structural mutants: helicity affects their interaction with the receptor.
Istituto Di Chimica Biomolecolare
Synthesis and separation of the enantiomers of the neuropeptide S receptor antagonist (9R/S)-3-oxo-1,1-diphenyl-tetrahydro-oxazolo[3,4-a]pyrazine-7-carboxylic acid 4-fluoro-benzylamide (SHA 68).
University of Ferrara
Further studies at neuropeptide s position 5: discovery of novel neuropeptide S receptor antagonists.
National Institute of Neuroscienc
Synthesis and biological activity of human neuropeptide S analogues modified in position 5: identification of potent and pure neuropeptide S receptor antagonists.
University of Ferrara
Tricyclic imidazole antagonists of the Neuropeptide S Receptor.
Merck Research Laboratories
Synthesis and pharmacological characterization of 5-phenyl-2-[2-(1-piperidinylcarbonyl)phenyl]-2,3-dihydro-1H-pyrrolo[1,2-c]imidazol-1-ones: a new class of Neuropeptide S antagonists.
Glaxosmithkline
Synthesis and evaluation of a new series of Neuropeptide S receptor antagonists.
Merck Research Laboratories
Preventing Morphine-Seeking Behavior through the Re-Engineering of Vincamine's Biological Activity.
University of Florida
Structure-activity study at positions 3 and 4 of human neuropeptide S.
University of Ferrara