Publication | Open Access
Design and Synthesis of a Novel Series of 1,2-Disubstituted Cyclopentanes as Small, Potent Potentiators of 2-Amino-3-(3-hydroxy-5-methyl-isoxazol-4-yl)propanoic Acid (AMPA) Receptors
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Citations
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References
2002
Year
Combinatorial ChemistryPotent PotentiatorsOrganic ChemistryPharmacotherapyChemistryHeterocycle ChemistryPharmaceutical ChemistryMedicinal ChemistryStereoselective SynthesisBiochemistryPharmacologyAmpa ReceptorsPropanoic AcidFunctional SelectivityNatural SciencesMedicineRelative StereochemistryDrug Discovery1,2-Disubstituted Cyclopentanes
2-Amino-3-(3-hydroxy-5-methyl-isoxazol-4-yl)propanoic acid (AMPA) potentiators are ligands that act as positive allosteric modulators at the AMPA receptors. We recently disclosed a novel series of 2-arylpropylsulfonamides that were potent potentiators of responses mediated through AMPA receptors. To further define the structural requirements for activity in this series, new ring-constrained analogues were prepared and a new stereocenter was introduced. The potentiating activity was highly dependent on the stereochemistry at the 2-position of the disubstituted cyclopentane and was independent of the relative stereochemistry at the 1-position. Compound (R,R)-10 represents a potent, novel potentiator of iGluR4 flip receptors (EC(50) = 22.6 nM).
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