Abstract
The synthesis and initial SAR studies of novel, highly potent positive allosteric modulators of AMPA receptors based on 3-(4-tert-butylphenyl)-4-cyano-5-methylsulfanyl-thiophene-2-carboxylic acid (6a) are described. SAR studies at the thioether moiety indicated that substitution at this position was mandatory and better potency was achieved with small groups.
MeSH terms
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Allosteric Regulation
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Carboxylic Acids
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Drug Design
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Excitatory Amino Acid Agents / chemical synthesis*
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Excitatory Amino Acid Agents / pharmacology
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Heterocyclic Compounds / chemical synthesis*
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Heterocyclic Compounds / pharmacology
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Humans
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Receptors, AMPA / drug effects*
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Structure-Activity Relationship
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Sulfides
Substances
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Carboxylic Acids
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Excitatory Amino Acid Agents
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Heterocyclic Compounds
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Receptors, AMPA
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Sulfides