Abstract
Hit compound 1, a selective noradrenaline re-uptake transporter (NET) inhibitor was optimised to build in potency at the serotonin re-uptake transporter (SERT) whilst maintaining selectivity against the dopamine re-uptake transporter (DAT). During the optimisation of 1 it became clear that selectivity against the Kv11.1 potassium ion channel (hERG) was also a parameter for optimisation within the series. Discrete structural changes to the molecule as well as a lowering of global cLogP successfully increased the hERG selectivity to afford compound 11 m, which was efficacious in a mouse model of inflammatory pain, complete Freund's adjuvant (CFA) induced thermal hyperalgesia and a rat model of neuropathic pain, spinal nerve ligation (SNL) induced mechanical allodynia.
Copyright © 2010 Elsevier Ltd. All rights reserved.
MeSH terms
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Animals
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Dopamine Plasma Membrane Transport Proteins / antagonists & inhibitors
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Dopamine Plasma Membrane Transport Proteins / metabolism
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ERG1 Potassium Channel
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Ether-A-Go-Go Potassium Channels / antagonists & inhibitors*
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Ether-A-Go-Go Potassium Channels / metabolism
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Male
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Mice
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Norepinephrine Plasma Membrane Transport Proteins / antagonists & inhibitors*
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Norepinephrine Plasma Membrane Transport Proteins / metabolism
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Pain / drug therapy
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Pyridines / chemical synthesis
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Pyridines / chemistry*
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Pyridines / therapeutic use
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Rats
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Rats, Wistar
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Selective Serotonin Reuptake Inhibitors / chemical synthesis
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Selective Serotonin Reuptake Inhibitors / chemistry*
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Selective Serotonin Reuptake Inhibitors / therapeutic use
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Serotonin Plasma Membrane Transport Proteins / chemistry*
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Serotonin Plasma Membrane Transport Proteins / metabolism
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Structure-Activity Relationship
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Tropanes / chemical synthesis
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Tropanes / chemistry*
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Tropanes / therapeutic use
Substances
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Dopamine Plasma Membrane Transport Proteins
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ERG1 Potassium Channel
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Ether-A-Go-Go Potassium Channels
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Norepinephrine Plasma Membrane Transport Proteins
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Pyridines
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Serotonin Plasma Membrane Transport Proteins
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Serotonin Uptake Inhibitors
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Tropanes