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Bioorganic & Medicinal Chemistry Letters|October 22, 2011
Synthesis and evaluation of pyridone-phenoxypropyl-R-2-methylpyrrolidine analogues as histamine H3 receptor antagonistsNadine C Becknell, Jacquelyn A Lyons, Lisa D Aimone, et al.
Bioorganic & Medicinal Chemistry Letters|August 8, 2006
Novel C-3 N-urea, amide, and carbamate dihydroindazolo[5,4-a]pyrrolo[3,4-c]carbazole analogs as potent TIE-2 and VEGF-R2 dual inhibitorsNadine C Becknell, Allison L Zulli, Thelma S Angeles, et al.
Bioorganic & Medicinal Chemistry Letters|September 28, 2011
Synthesis and evaluation of pyridazinone-phenethylamine derivatives as selective and orally bioavailable histamine H3 receptor antagonists with robust wake-promoting activityReddeppa Reddy Dandu, John A Gruner, Joanne R Mathiasen, et al.
Bioorganic & Medicinal Chemistry Letters|March 18, 2008
TIE-2/VEGF-R2 SAR and in vitro activity of C3-acyl dihydroindazolo[5,4-a]pyrrolo[3,4-c]carbazole analogsTed L Underiner, Bruce Ruggeri, Lisa Aimone, et al.
Bioorganic & Medicinal Chemistry Letters|December 7, 2011
4,5-dihydropyridazin-3-one derivatives as histamine H₃ receptor inverse agonistsRobert L Hudkins, Lisa D Aimone, Reddeppa Reddy Dandu, et al.
Bioorganic & Medicinal Chemistry Letters|February 1, 2012
4-phenoxypiperidine pyridazin-3-one histamine H(3) receptor inverse agonists demonstrating potent and robust wake promoting activityRobert L Hudkins, Allison L Zulli, Reddeppa reddy Dandu, et al.
Bioorganic & Medicinal Chemistry Letters|May 1, 2010
8-THP-DHI analogs as potent Type I dual TIE-2/VEGF-R2 receptor tyrosine kinase inhibitorsRobert L Hudkins, Allison L Zulli, Ted L Underiner, et al.
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