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Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport

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Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
Molecular pharmacology of glutamate transporters, EAATs and VGLUTs - ScienceDirect
Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
Molecular pharmacology of glutamate transporters, EAATs and VGLUTs - ScienceDirect
Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
PDF) Substituted Amides of Pyrazine-2-carboxylic acids: Synthesis and Biological Activity
Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
Inhibition of the Vesicular Glutamate Transporter (VGLUT) with Congo Red Analogs: New Binding Insights
Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
Visible-light-induced and copper-catalyzed oxidative cyclization of substituted o -aminophenylacetylene for the synthesis of quinoline and indole deri - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/D1QO00914A
Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
Visible-light-induced and copper-catalyzed oxidative cyclization of substituted o -aminophenylacetylene for the synthesis of quinoline and indole deri - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/D1QO00914A
Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
Frontiers Are vesicular neurotransmitter transporters potential treatment targets for temporal lobe epilepsy?
Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
VGLUT substrates and inhibitors: A computational viewpoint - ScienceDirect
Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
Vesicular Neurotransmitter Transporters
Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
Richard J. Bridges's research works University of Montana, Missoula (UMT) and other places
Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
Frontiers Are vesicular neurotransmitter transporters potential treatment targets for temporal lobe epilepsy?
Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
Leveraging VGLUT3 Functions to Untangle Brain Dysfunctions: Trends in Pharmacological Sciences
Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
Leveraging VGLUT3 Functions to Untangle Brain Dysfunctions: Trends in Pharmacological Sciences
Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
Vesicular Neurotransmitter Transporters
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