Search Results - "Schrøder, Tenna J"

Novel Aza-analogous Ergoline Derived Scaffolds as Potent Serotonin 5‑HT6 and Dopamine D2 Receptor Ligands by Krogsgaard-Larsen, Niels, Jensen, Anders A, Schrøder, Tenna J, Christoffersen, Claus. T, Kehler, Jan

“…By introducing distal substituents on a tetracyclic scaffold resembling the ergoline structure, two series of analogues were achieved exhibiting subnanomolar…”
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Discovery of phosphoric acid mono-{2-[(E/Z)-4-(3,3-dimethyl-butyrylamino)-3,5-difluoro-benzoylimino]-thiazol-3-ylmethyl} ester (Lu AA47070): a phosphonooxymethylene prodrug of a potent and selective hA(2A) receptor antagonist by Sams, Anette G, Mikkelsen, Gitte K, Larsen, Mogens, Langgård, Morten, Howells, Mark E, Schrøder, Tenna J, Brennum, Lise T, Torup, Lars, Jørgensen, Erling B, Bundgaard, Christoffer, Kreilgård, Mads, Bang-Andersen, Benny

“…The discovery and structure-activity relationship of a series of hA(2A) receptor antagonists is described. Compound 28 was selected from the series as a potent…”
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Novel Aza-analogous Ergoline Derived Scaffolds as Potent Serotonin 5-HT 6 and Dopamine D 2 Receptor Ligands by Krogsgaard-Larsen, Niels, Jensen, Anders A., Schrøder, Tenna J., Christoffersen, Claus. T., Kehler, Jan

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Discovery of Phosphoric Acid Mono-{2-[( E / Z )-4-(3,3-dimethyl-butyrylamino)-3,5-difluoro-benzoylimino]-thiazol-3-ylmethyl} Ester (Lu AA47070): A Phosphonooxymethylene Prodrug of a Potent and Selective hA 2A Receptor Antagonist by Sams, Anette G., Mikkelsen, Gitte K., Larsen, Mogens, Langgård, Morten, Howells, Mark E., Schrøder, Tenna J., Brennum, Lise T., Torup, Lars, Jørgensen, Erling B., Bundgaard, Christoffer, Kreilgård, Mads, Bang-Andersen, Benny

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Discovery of Phosphoric Acid Mono-{2-[(E/Z)-4-(3,3-dimethyl-butyrylamino)-3,5-difluoro-benzoylimino]-thiazol-3-ylmethyl} Ester (Lu AA47070): A Phosphonooxymethylene Prodrug of a Potent and Selective hA2A Receptor Antagonist by Sams, Anette G, Mikkelsen, Gitte K, Larsen, Mogens, Langgård, Morten, Howells, Mark E, Schrøder, Tenna J, Brennum, Lise T, Torup, Lars, Jørgensen, Erling B, Bundgaard, Christoffer, Kreilgård, Mads, Bang-Andersen, Benny

“…The discovery and structure−activity relationship of a series of hA2A receptor antagonists is described. Compound 28 was selected from the series as a potent…”
Get full text