| Literature DB >> 31857840 |
Daniel D Long1, Scott R Armstrong1, David T Beattie1, Christina B Campbell1, Timothy J Church1, Pierre-Jean Colson1, Sean M Dalziel1, John R Jacobsen1, Lan Jiang1, Glenmar P Obedencio1, Miroslav Rapta1, Daisuke Saito1, Ioanna Stergiades1, Pamela R Tsuruda1, Priscilla M Van Dyke1, Ross G Vickery1.
Abstract
The effects of opioids in the central nervous system (CNS) provide significant benefit in the treatment of pain but can also lead to physical dependence and addiction, which has contributed to a growing opioid epidemic in the United States. Gastrointestinal dysfunction is an additional serious consequence of opioid use, and this can be treated with a localized drug distribution of a non-CNS penetrant, peripherally restricted opioid receptor antagonist. Herein, we describe the application of Theravance's multivalent approach to drug discovery coupled with a physicochemical property design strategy by which the N-substituted-endo-3-(8-aza-bicyclo[3.2.1]oct-3-yl)-phenyl carboxamide series of μ-opioid receptor antagonists was optimized to afford the orally absorbed, non-CNS penetrant, Phase 3 ready clinical compound axelopran (TD-1211) 19i as a potential treatment for opioid-induced constipation.Entities:
Year: 2019 PMID: 31857840 PMCID: PMC6912869 DOI: 10.1021/acsmedchemlett.9b00406
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345