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The Importance of the 6- and 7-Positions of Tetrahydroisoquinolines as Selective Antagonists for the Orexin 1 Receptor
Selective antagonism of the orexin 1 (OX(1)) receptor has been proposed as a potential mechanism for treatment of drug addiction. We have previously reported studies on the structure-activity relationships of tetrahydroisoquinoline-based antagonists. In this report, we elucidated the respective role...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Bioorg Med Chem |
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| Κύριοι συγγραφείς: | , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2015
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4554834/ https://ncbi.nlm.nih.gov/pubmed/26216017 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmc.2015.07.013 |
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