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

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Last updated 12 abril 2025
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
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
Pharmacology of Neurotransmitter Transport into Secretory Vesicles
Synthesis and in Vitro Pharmacology of Substituted  Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate  Transport
PDF) Pharmacology of Neurotransmitter Transport into Secretory Vesicles
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
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
Design, synthesis and biological evaluation of small-azo-dyes as potent Vesicular Glutamate Transporters inhibitors - ScienceDirect
Synthesis and in Vitro Pharmacology of Substituted  Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate  Transport
LSP5-2157 a new inhibitor of vesicular glutamate transporters - ScienceDirect
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
Green Design, Synthesis, and Molecular Docking Study of Novel Quinoxaline Derivatives with Insecticidal Potential against Aphis craccivora
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
Molecular, Structural, Functional, and Pharmacological Sites for Vesicular Glutamate Transporter Regulation. - Abstract - Europe PMC
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
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
Modulation of Hippocampal Synaptic Transmission by the Kynurenine Pathway Member Xanthurenic Acid and Other VGLUT Inhibitors

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