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
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
SLC transporters as therapeutic targets: emerging opportunities
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
Synthesis and in Vitro Pharmacology of Substituted  Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate  Transport
US8802853B2 - Arylalkenyl and arylalkynyl substituted imidazoquinolines - Google Patents
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
Development of a Robust Synthesis of Dactolisib on a Commercial Manufacturing Scale
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
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
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
Leveraging VGLUT3 Functions to Untangle Brain Dysfunctions: Trends in Pharmacological Sciences
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