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Design, synthesis, and pharmacological characterization of N- and O-substituted 5,6,7,8-tetrahydro-4H-isoxazolo[4,5-d]azepin-3-ol analogues: novel 5-HT(2A)/5-HT(2C) receptor agonists with pro-cognitive properties.
Jensen AA, Plath N, Pedersen MH, Isberg V, Krall J, Wellendorph P, Stensbøl TB, Gloriam DE, Krogsgaard-Larsen P, Frølund B. Jensen AA, et al. Among authors: wellendorph p. J Med Chem. 2013 Feb 14;56(3):1211-27. doi: 10.1021/jm301656h. Epub 2013 Jan 17. J Med Chem. 2013. PMID: 23301527
Design, synthesis, and in vitro pharmacology of new radiolabeled gamma-hydroxybutyric acid analogues including photolabile analogues with irreversible binding to the high-affinity gamma-hydroxybutyric acid binding sites.
Sabbatini P, Wellendorph P, Høg S, Pedersen MH, Bräuner-Osborne H, Martiny L, Frølund B, Clausen RP. Sabbatini P, et al. Among authors: wellendorph p. J Med Chem. 2010 Sep 9;53(17):6506-10. doi: 10.1021/jm1006325. J Med Chem. 2010. PMID: 20715819
Chemogenomic discovery of allosteric antagonists at the GPRC6A receptor.
Gloriam DE, Wellendorph P, Johansen LD, Thomsen AR, Phonekeo K, Pedersen DS, Bräuner-Osborne H. Gloriam DE, et al. Among authors: wellendorph p. Chem Biol. 2011 Nov 23;18(11):1489-98. doi: 10.1016/j.chembiol.2011.09.012. Chem Biol. 2011. PMID: 22118683
94 results