Results
1 -
10 of
10
(Click
here to explore results)
- Selectivity profile comparison for certain γ-butyrolactone and oxazolidinone-based ligands on a sigma 2 receptor over sigma 1: a molecular docking approach. Richie R. Bhandare, Dilep Kumar Sigalapalli, Afzal B. Shaik, Daniel J. Canney, Benjamin E. Blass
, RSC Adv.
, 2022
, 12
, 20096
- Stereoselective synthesis of conformationally restricted KOR agonists based on the 2,5-diazabicyclo[2.2.2]octane scaffold. Christian Wittig, Dirk Schepmann, Michael Soeberdt, Constantin G. Daniliuc, Bernhard Wünsch
, Org. Biomol. Chem.
, 2017
, 15
, 6520
- Diastereoselective synthesis of conformationally restricted KOR agonists. Denise Ilari, Sarah Maskri, Dirk Schepmann, Jens Köhler, Constantin G. Daniliuc, Oliver Koch, Bernhard Wünsch
, Org. Biomol. Chem.
, 2021
, 19
, 4082
- Biosynthesis and synthetic biology of psychoactive natural products. Cooper S. Jamieson, Joshua Misa, Yi Tang, John M. Billingsley
, Chem. Soc. Rev.
, 2021
, 50
, 6950
- Synthesis and pharmacological evaluation of like- and unlike-configured tetrahydro-2-benzazepines with the α-substituted benzyl moiety in the 5-position. Peer Hasebein, Bastian Frehland, Kirstin Lehmkuhl, Roland Fröhlich, Dirk Schepmann, Bernhard Wünsch
, Org. Biomol. Chem.
, 2014
, 12
, 5407
- Effects of polar κ receptor agonists designed for the periphery on ATP-induced Ca2+ release from keratinocytes. Fabian Galla, Christian Bourgeois, Kirstin Lehmkuhl, Dirk Schepmann, Michael Soeberdt, Tobias Lotts, Christoph Abels, Sonja Ständer, Bernhard Wünsch
, Med. Chem. Commun.
, 2016
, 7
, 317
- Synthesis and pharmacological evaluation of enantiomerically pure endo-configured KOR agonists with 2-azabicyclo[3.2.1]octane scaffold. Hendrik Jonas, Daniele Aiello, Bastian Frehland, Kirstin Lehmkuhl, Dirk Schepmann, Jens Köhler, Patrizia Diana, Bernhard Wünsch
, Org. Biomol. Chem.
, 2021
, 19
, 8384
- New therapeutic potential for psychoactive natural products. Katherine M. Prevatt-Smith, Thomas E. Prisinzano
, Nat. Prod. Rep.
, 2010
, 27
, 23
- Molecular determinants for drug–receptor interactions. Part 13. X-Ray molecular structure of naltrexone malonate and quantum chemical studies of the conformations of the pure narcotic antagonists naloxone and naltrexone. Maria E. Amato, Giuliano Bandoli, Antonio Grassi, Marino Nicolini, Giuseppe C. Pappalardo
, J. Chem. Soc., Perkin Trans. 2
, 1990
, 1757
- Synthesis, antinociceptive activity, and opioid receptor profiles of 10-substituted-6-oxamorphinans. Andrew B. McElroy, David E. Bays, David I. C. Scopes, Ann G. Hayes, Michael J. Sheehan
, J. Chem. Soc., Perkin Trans. 1
, 1990
, 1563