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Identification of pyridazin-3-one derivatives as potent, selective histamine H₃ receptor inverse agonists with robust wake activity.
Bioorg Med Chem Lett. 2011 Sep 15;21(18):5493-7. doi: 10.1016/j.bmcl.2011.06.108. Epub 2011 Jun 30.
Bioorg Med Chem Lett. 2011.
PMID: 21782432
Amine-constrained pyridazinone histamine H₃ receptor antagonists.
Sundar BG, Bailey T, Bacon E, Aimone L, Huang Z, Lyons J, Raddatz R, Hudkins R.
Sundar BG, et al.
Bioorg Med Chem Lett. 2011 Sep 15;21(18):5543-6. doi: 10.1016/j.bmcl.2011.06.094. Epub 2011 Jul 22.
Bioorg Med Chem Lett. 2011.
PMID: 21824776
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Novel brain penetrant benzofuropiperidine 5-HT₆ receptor antagonists.
Sundar BG, Bailey TR, Dunn DD, Bacon ER, Salvino JM, Morton GC, Aimone LD, Zeqi H, Mathiasen JR, Dicamillo A, Huffman MJ, McKenna BA, Kopec K, Lu LD, Brown R, Qian J, Angeles T, Connors T, Spais C, Holskin B, Galinis D, Duzic E, Schaffhauser H, Rosse GC.
Sundar BG, et al.
Bioorg Med Chem Lett. 2012 Jan 1;22(1):120-3. doi: 10.1016/j.bmcl.2011.11.050. Epub 2011 Nov 22.
Bioorg Med Chem Lett. 2012.
PMID: 22153937
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Novel morpholine ketone analogs as potent histamine H3 receptor inverse agonists with wake activity.
Sundar BG, Bailey TR, Dunn D, Hostetler GA, Chatterjee S, Bacon ER, Yue C, Schweizer D, Aimone LD, Gruner JA, Lyons J, Raddatz R, Lesur B.
Sundar BG, et al.
Bioorg Med Chem Lett. 2012 Feb 15;22(4):1546-9. doi: 10.1016/j.bmcl.2012.01.004. Epub 2012 Jan 10.
Bioorg Med Chem Lett. 2012.
PMID: 22297111
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