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Effect of 1-Substitution on Tetrahydroisoquinolines as Selective Antagonists for the Orexin-1 Receptor

Selective blockade of the Orexin-1 receptor has been suggested as a potential approach to drug addiction therapy because of its role in modulating the brain's reward system. We have recently reported a series of tetrahydroisoquinoline-based OX(1) selective antagonists. Aimed at elucidating SAR...

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Détails bibliographiques
Publié dans:ACS Chem Neurosci
Auteurs principaux: Perrey, David A., German, Nadezhda A., Decker, Ann M., Thorn, David, Li, Jun-Xu, Gilmour, Brian P., Thomas, Brian F., Harris, Danni L., Runyon, Scott P., Zhang, Yanan
Format: Artigo
Langue:Inglês
Publié: 2015
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4400266/
https://ncbi.nlm.nih.gov/pubmed/25643283
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/cn500330v
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