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Journal Abstract Search

138 related items for PubMed ID: 28212021

  • 21.
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  • 22. Novel difluoromethyl-containing 1-((4-methoxy-3-(piperazin-1-yl)phenyl)sulfonyl)-1H-indole scaffold as potent 5-HT6R antagonists: Design, synthesis, biological evaluation, and early in vivo cognition-enhancing studies.
    Yi C, Xue Y, Chen K, Wang T, Yu J, Wang Z, Jin C.
    Bioorg Med Chem; 2022 Sep 15; 70():116917. PubMed ID: 35839536
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  • 23. Epiminocyclohepta[b]indole analogs as 5-HT6 antagonists.
    Henderson AJ, Guzzo PR, Ghosh A, Kaur J, Koo JM, Nacro K, Panduga S, Pathak R, Shimpukade B, Tan V, Xiang K, Wierschke JD, Isherwood ML.
    Bioorg Med Chem Lett; 2012 Feb 15; 22(4):1494-8. PubMed ID: 22290076
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  • 24. Idalopirdine as a treatment for Alzheimer's disease.
    Galimberti D, Scarpini E.
    Expert Opin Investig Drugs; 2015 Feb 15; 24(7):981-7. PubMed ID: 26022777
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  • 30. New 1-arylindoles based serotonin 5-HT7 antagonists. Synthesis and binding evaluation studies.
    Sagnes C, Fournet G, Satala G, Bojarski AJ, Joseph B.
    Eur J Med Chem; 2014 Mar 21; 75():159-68. PubMed ID: 24531229
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  • 31. The 5-HT6 receptor antagonist idalopirdine potentiates the effects of acetylcholinesterase inhibition on neuronal network oscillations and extracellular acetylcholine levels in the rat dorsal hippocampus.
    Herrik KF, Mørk A, Richard N, Bundgaard C, Bastlund JF, de Jong IEM.
    Neuropharmacology; 2016 Aug 21; 107():351-363. PubMed ID: 27039041
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  • 32. Effects of ST1936, a selective serotonin-6 agonist, on electrical activity of putative mesencephalic dopaminergic neurons in the rat brain.
    Borsini F, Bordi F, Poggi A, Di Matteo V.
    J Psychopharmacol; 2015 Jul 21; 29(7):802-11. PubMed ID: 25735994
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  • 33.
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  • 34. Dimebolin is a 5-HT6 antagonist with acute cognition enhancing activities.
    Schaffhauser H, Mathiasen JR, Dicamillo A, Huffman MJ, Lu LD, McKenna BA, Qian J, Marino MJ.
    Biochem Pharmacol; 2009 Oct 15; 78(8):1035-42. PubMed ID: 19549510
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  • 36. Investigational drugs targeting 5-HT6 receptors for the treatment of Alzheimer's disease.
    Wicke K, Haupt A, Bespalov A.
    Expert Opin Investig Drugs; 2015 Oct 15; 24(12):1515-28. PubMed ID: 26548316
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  • 37. 5-HT1A and 5-HT2A receptor affinity and functional profile of some N-[3-(4-aryl-1-piperazinyl)propyl] derivatives of indolin-2(1H)-one, quinolin-2(1 H)-one and isoquinolin-1(2H)-one. Part 30: Structure-activity relationship studies of CNS agents.
    Mokrosz MJ, Mokrosz JL, Duszyńska B, Dereń-Wesołek A, Kłodzińska A, Kowalski P, Charakchieva-Minol S, Tatarczyńska E, Kowalska T, Majka Z, Chojnacka-Wójcik E, Misztal S.
    Pharmazie; 1997 Jun 15; 52(6):423-8. PubMed ID: 9260266
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  • 40. G-protein activation at 5-HT1A receptors by the 5-ht1F ligand LY334370 in guinea-pig brain sections and recombinant cell lines.
    Dupuis DS, Colpaert FC, Pauwels PJ.
    Br J Pharmacol; 1998 May 15; 124(2):283-90. PubMed ID: 9641544
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