Synthesis and in Vitro Pharmacology of Substituted Quinoline-2,4-dicarboxylic Acids as Inhibitors of Vesicular Glutamate Transport
Por um escritor misterioso
Last updated 20 setembro 2024
Design and Synthesis of Systemically Active Metabotropic Glutamate Subtype-2 and -3 (mGlu2/3) Receptor Positive Allosteric Modulators (PAMs): Pharmacological Characterization and Assessment in a Rat Model of Cocaine Dependence
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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
Structure‐Activity‐Relationship‐Aided Design and Synthesis of xCT Antiporter Inhibitors - Cirillo - 2021 - ChemMedChem - Wiley Online Library
Molecular pharmacology of glutamate transporters, EAATs and VGLUTs - ScienceDirect
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