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Agonists and Antagonists for Group III Metabotropic Glutamate Receptors 6, 7 and 8
Current Topics in Medicinal Chemistry, 2005Metabotropic glutamate receptors (mGluRs) have been implicated in a variety of neurological and psychiatric disorders. This article describes recent progress in the development of agonists and antagonists for mGluR 6, 7, and 8. All of them are conformationally constrained or substituted amino acids, and they act at N-terminal extracellular glutamate ...
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Neuroscience Letters, 2010
There is increasing evidence to suggest that metabotropic glutamate (mGlu) receptors including mGlu(7) receptor are important in the pathophysiology of stress-related psychiatric disorders such as anxiety and major depression. mGlu(7) receptor is highly expressed in the hippocampus, a key region involved in the modulation of depression-related ...
John F. Cryan+3 more
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There is increasing evidence to suggest that metabotropic glutamate (mGlu) receptors including mGlu(7) receptor are important in the pathophysiology of stress-related psychiatric disorders such as anxiety and major depression. mGlu(7) receptor is highly expressed in the hippocampus, a key region involved in the modulation of depression-related ...
John F. Cryan+3 more
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Molecular Pharmacology, 2002
Presynaptic metabotropic glutamate receptors (mGluRs) often act as feedback inhibitors of synaptic transmission and serve important roles in defining the activity of glutamatergic synapses.
S. Sorensen+4 more
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Presynaptic metabotropic glutamate receptors (mGluRs) often act as feedback inhibitors of synaptic transmission and serve important roles in defining the activity of glutamatergic synapses.
S. Sorensen+4 more
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Bioorganic & Medicinal Chemistry Letters, 2007
Rational replacement of the alkyne linker of mGluR5 antagonist MPEP gave 7-arylquinolines. SAR optimization gave an orally active compound with high affinity for the MPEP binding site.
Kristen K. Gillespie+18 more
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Rational replacement of the alkyne linker of mGluR5 antagonist MPEP gave 7-arylquinolines. SAR optimization gave an orally active compound with high affinity for the MPEP binding site.
Kristen K. Gillespie+18 more
openaire +3 more sources
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 2015
Yi Liu+8 more
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Yi Liu+8 more
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