Description of impact
Original basic research on melatonin receptors undertaken at the Rowett Institute, University of Aberdeen, and funded by the Scottish Government, provided the opportunity for Servier pharmaceuticals to develop a new line of therapeutics for depression.The company exploited Rowett know-how and invested in new research to develop a new line of compounds and to understand their structure-function relationships. This work enabled the development of melatonin analogues for clinical trials and ultimately led to the development of melatonin compounds for treatment of circadian related disorders.
One (S20098) was identified as having positive effects for disrupted circadian rhythms and beneficial outcomes for patients with depression. S20098 (also known as Agomelatine) was launched after EU authorization in 2009 as a novel anti-depressant drug called Valdoxan®. Today Valdoxan is an award winning anti-depressant drug recognised for its novel mechanism of action and few side effects. Valdoxan is the only anti-depressant drug to be brought to the market in the last 10 years. In summary, supported by investment from industry research undertaken at the University of Aberdeen contributed to the development of a novel antidepressant drug that provides a new clinical intervention with advantages over previously available antidepressants that will make a significant impact on the health and well-being of those afflicted by depression.
Impact status | Impact Completed (Open) |
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Category of impact | Health and Wellbeing |
Documents & Links
Related content
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Research output
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Characterisation of human melatonin mt(1) and MT2 receptors by CRE-luciferase reporter assay
Research output: Contribution to journal › Article › peer-review
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The roles of valine 208 and histidine 211 in ligand binding and receptor function of the ovine Mel(1a beta) melatonin receptor
Research output: Contribution to journal › Article › peer-review
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Chimeric melatonin mt(1) and melatonin-related receptors Identification of domains and residues participating in ligand binding and receptor activation of the melatonin mt(1) receptor
Research output: Contribution to journal › Article › peer-review
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Cloning and functional analysis of a polymorphic variant of the ovine Mel 1a melatonin receptor
Research output: Contribution to journal › Article › peer-review
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Serine residues 110 and 114 are required for agonist binding but not antagonist binding to the melatonin MT1 receptor
Research output: Contribution to journal › Article › peer-review