Abstract
Pyridineethanolamine derivatives containing cyanoguanidine or nitroethylenediamine moieties were examined as human beta3 adrenergic receptor (AR) agonists. Notably, indoline derivatives 6a and 11 were potent beta3 AR agonists (beta3 EC50 = 13 and 19 nM, respectively), which showed good selectivity over binding to and minimal activation of the beta1 and beta2 ARs.
MeSH terms
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Adenylyl Cyclases / drug effects
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Adenylyl Cyclases / metabolism
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Adrenergic beta-3 Receptor Agonists*
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Adrenergic beta-Agonists / chemical synthesis*
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Adrenergic beta-Agonists / chemistry
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Adrenergic beta-Agonists / pharmacology
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Animals
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CHO Cells
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Cell Membrane / chemistry
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Combinatorial Chemistry Techniques
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Cricetinae
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Diamines / chemistry
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Ethane / analogs & derivatives
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Ethane / chemistry
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Guanidines / chemistry
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Humans
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Inhibitory Concentration 50
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Nitroparaffins / chemistry
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Radioligand Assay
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Receptors, Adrenergic, beta / metabolism
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Receptors, Adrenergic, beta-3 / metabolism
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Structure-Activity Relationship
Substances
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Adrenergic beta-3 Receptor Agonists
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Adrenergic beta-Agonists
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Diamines
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Guanidines
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Nitroparaffins
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Receptors, Adrenergic, beta
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Receptors, Adrenergic, beta-3
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nitroethane
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Adenylyl Cyclases
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Ethane
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dicyandiamido