Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
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Last updated 03 abril 2025

Molecules May-1 2023 - Browse Articles

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Discovery of CVN636: A Highly Potent, Selective, and CNS Penetrant mGluR7 Allosteric Agonist

Vesicular Neurotransmitter Transporters

Frontiers Are vesicular neurotransmitter transporters potential treatment targets for temporal lobe epilepsy?

Biomolecules, Free Full-Text

Buy 1-(Cyclohexyloxy)-4-nitrobenzene, 5493-73-2

Design, synthesis and biological evaluation of small-azo-dyes as potent Vesicular Glutamate Transporters inhibitors - ScienceDirect

Molecular pharmacology of glutamate transporters, EAATs and VGLUTs - ScienceDirect

Inhibition of the Vesicular Glutamate Transporter (VGLUT) with Congo Red Analogs: New Binding Insights

Leveraging VGLUT3 Functions to Untangle Brain Dysfunctions: Trends in Pharmacological Sciences

Vesicular Neurotransmitter Transporters

Molecular, Structural, Functional, and Pharmacological Sites for Vesicular Glutamate Transporter Regulation

Synthesis and biological evaluations of N′-substituted methylene-4-( quinoline-4-amino) benzoylhydrazides as potential anti-hepatoma agents - ScienceDirect

Molecular pharmacology of glutamate transporters, EAATs and VGLUTs - ScienceDirect
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