Zobrazeno 1 - 10
of 2 670
pro vyhledávání: '"M St.-Onge"'
Autor:
Flammia, Rachael, Huang, Boshi, Pagare, Piyusha P., M. St. Onge, Celsey, Abebayehu, Abeje, Gillespie, James C., Mendez, Rolando E., Selley, Dana E., Dewey, William L., Zhang, Yan
Publikováno v:
In Bioorganic Chemistry July 2024 148
Publikováno v:
Molecules, Vol 29, Iss 14, p 3331 (2024)
We recently developed a series of nalfurafine analogs (TK10, TK33, and TK35) that may serve as non-addictive candidate analgesics. These compounds are mixed-action agonists at the kappa and delta opioid receptors (KOR and DOR, respectively) and produ
Externí odkaz:
https://doaj.org/article/3bd22c861a0e4555aaa74314112260cd
Autor:
Daniel Côté
Publikováno v:
Service social. 55:116
Autor:
Sylvie Corbeil, Carole Sénéchal
Publikováno v:
Revue de psychoéducation. 37:313
Publikováno v:
The Quarterly Review of Biology, 1975 Dec 01. 50(4), 497-497.
Externí odkaz:
https://www.jstor.org/stable/2821580
Autor:
E A de Kemp, H A J Russell, B Brodaric, D B Snyder, M J Hillier, M St-Onge, C Harrison, D Paul, A Vaillancourt, K Bédard, A Mort, E M Schetselaar, D White, C Logan, A Ashoori Pareshkoohi
Application of 3D technologies to the wide range of Geosciences knowledge domains is well underway. These have been operationalized in workflows of the hydrocarbon sector for a half-century, and now in mining for over two decades. In Geosciences, alg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6e1b7574181025ecd6998a0709bd63b
https://doi.org/10.4095/331871
https://doi.org/10.4095/331871
Akademický článek
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Publikováno v:
Pharmacology, biochemistry, and behavior. 221
Recent studies have shown that social interaction can serve as an alternative reinforcer to opioid self-administration under a choice context in rats. However, additional parametric studies are needed to evaluate the sensitivity of opioid-vs.-social
Publikováno v:
Journal of molecular graphicsmodelling. 116
Lysophosphatidic acid receptor 4 (LPA
Publikováno v:
Tetrahedron Lett
Methodology is presented for the synthesis of 6α/β−3-dehydroxynaltrexamines and 6α/β-N-methyl-3-dehydroxynaltrexamines. A stereoselective route is provided for each target compound while a novel one-pot method for the synthesis of 6α/β−3-N-