Abstract
A new synthesis of (R,S)-PPG (4-phosphonophenylglycine) and the separation of the protected enantiomers leading after deprotection to (+)- and (-)-PPG are described. Pharmacological characterization at the group III metabotropic glutamate receptors hmGluR4a and hmGluR7b revealed (+)-PPG as the active enantiomer.
MeSH terms
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Excitatory Amino Acid Agonists / pharmacology*
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Glycine / analogs & derivatives*
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Glycine / chemical synthesis
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Glycine / chemistry
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Glycine / pharmacology
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Receptors, Metabotropic Glutamate / agonists*
Substances
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4-phosphonophenylglycine
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Excitatory Amino Acid Agonists
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Receptors, Metabotropic Glutamate
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Glycine