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About:Tedatioxetine

An Entity of Type:chemical substance,from Named Graph:http://dbpedia.org,within Data Space:dbpedia.org

Tedatioxetine (developmental code name Lu AA24530) is an experimental antidepressant that was discovered by scientists at Lundbeck; in 2007 Lundbeck and Takeda entered into a partnership that included tedatioxetine but was focused on another, more advanced Lundbeck drug candidate, vortioxetine. Tedatioxetine is reported to act as a triple reuptake inhibitor (serotonin > norepinephrine > dopamine) and 5-HT2A, 5-HT2C, 5-HT3, and α1A-adrenergic receptor antagonist. On May 10, 2016, all work on tedatioxetine stopped.

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  • Tedatioxetine (developmental code name Lu AA24530) is an experimental antidepressant that was discovered by scientists at Lundbeck; in 2007 Lundbeck and Takeda entered into a partnership that included tedatioxetine but was focused on another, more advanced Lundbeck drug candidate, vortioxetine. Tedatioxetine is reported to act as a triple reuptake inhibitor (serotonin > norepinephrine > dopamine) and 5-HT2A, 5-HT2C, 5-HT3, and α1A-adrenergic receptor antagonist. As of 2009, it was in phase II clinical trials for major depressive disorder, but there have been no updates since then, and as of August 2013 it was no longer displayed on Lundbeck's product pipeline. On May 10, 2016, all work on tedatioxetine stopped. A Chinese patent shows that there has been interest in this compound outside of Lundbeck. (en)
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  • 508233-95-2
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  • 5H681S8O3S
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  • D10170
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  • 9878913
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  • File:Tedatioxetine ball-and-stick model.png (en)
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  • D10170 (en)
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  • Investigational (en)
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  • Lu AA24530; Lu-AA-24530 (en)
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  • Tedatioxetine (developmental code name Lu AA24530) is an experimental antidepressant that was discovered by scientists at Lundbeck; in 2007 Lundbeck and Takeda entered into a partnership that included tedatioxetine but was focused on another, more advanced Lundbeck drug candidate, vortioxetine. Tedatioxetine is reported to act as a triple reuptake inhibitor (serotonin > norepinephrine > dopamine) and 5-HT2A, 5-HT2C, 5-HT3, and α1A-adrenergic receptor antagonist. On May 10, 2016, all work on tedatioxetine stopped. (en)
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  • Tedatioxetine (en)
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