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1
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Structural features for functional selectivity at serotonin receptors.
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Science
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2013
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2.60
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2
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Structural basis for molecular recognition at serotonin receptors.
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Science
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2013
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1.86
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3
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Extensive rigid analogue design maps the binding conformation of potent N-benzylphenethylamine 5-HT2A serotonin receptor agonist ligands.
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ACS Chem Neurosci
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2012
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0.96
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4
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Comparison of the enantiomers of (+/-)-doxanthrine, a high efficacy full dopamine D(1) receptor agonist, and a reversal of enantioselectivity at D(1) versus alpha(2C) adrenergic receptors.
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Eur Neuropsychopharmacol
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2008
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0.81
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5
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Assessment of dopamine D₁ receptor affinity and efficacy of three tetracyclic conformationally-restricted analogs of SKF38393.
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Bioorg Med Chem
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2011
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0.79
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6
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trans-2-(2,5-Dimethoxy-4-iodophenyl)cyclopropylamine and trans-2-(2,5-dimethoxy-4-bromophenyl)cyclopropylamine as potent agonists for the 5-HT(2) receptor family.
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Beilstein J Org Chem
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2012
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0.79
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7
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Identification of a 2-phenyl-substituted octahydrobenzo[f]quinoline as a dopamine D₃ receptor-selective full agonist ligand.
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Bioorg Med Chem
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2012
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0.75
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8
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Design and Discovery of Functionally Selective Serotonin 2C (5-HT2C) Receptor Agonists.
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J Med Chem
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2016
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0.75
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