Abstract
Structural modification of a virtual screening hit led to the identification of a new series of 4-[3-aryl-2,2-dioxido-2,1,3-benzothiadiazol-1(3H)-yl]-1-(methylamino)butan-2-ols which are potent and selective inhibitors of the norepinephrine transporter over both the serotonin and dopamine transporters. One representative compound S-17b (WYE-103231) had low nanomolar hNET potency (IC(50) = 1.2 nM) and excellent selectivity for hNET over hSERT (>1600-fold) and hDAT (>600-fold). S-17b additionally had a good pharmacokinetic profile and demonstrated oral efficacy in rat models of ovariectomized-induced thermoregulatory dysfunction and morphine dependent flush as well as the hot plate and spinal nerve ligation (SNL) models of acute and neuropathic pain.
MeSH terms
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Animals
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Cell Line
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Cyclic S-Oxides / chemical synthesis
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Cyclic S-Oxides / chemistry*
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Cyclic S-Oxides / pharmacokinetics
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Cyclic S-Oxides / pharmacology*
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Drug Discovery / methods*
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Female
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Humans
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Male
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Neurotransmitter Uptake Inhibitors / chemical synthesis
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Neurotransmitter Uptake Inhibitors / chemistry*
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Neurotransmitter Uptake Inhibitors / pharmacokinetics
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Neurotransmitter Uptake Inhibitors / pharmacology*
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Norepinephrine / metabolism*
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Rats
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Structure-Activity Relationship
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Thiadiazoles / chemical synthesis
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Thiadiazoles / chemistry*
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Thiadiazoles / pharmacokinetics
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Thiadiazoles / pharmacology*
Substances
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4-(3-(2-fluorophenyl)-2,2-dioxido-2,1,3-benzothiadiazol-1(3H)-yl)-1-(methylamino)butan-2-ol
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Cyclic S-Oxides
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Neurotransmitter Uptake Inhibitors
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Thiadiazoles
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benzo-1,2,3-thiadiazole
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Norepinephrine