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

Por um escritor misterioso

Descrição

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
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
Synthesis, in vitro inhibitor screening, structure–activity relationship, and molecular dynamic simulation studies of novel thioquinoline derivatives as potent α-glucosidase inhibitors
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
Molecules, Free Full-Text
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
Christina N Carrigan'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
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
Synthesis and biological evaluations of N′-substituted methylene-4-( quinoline-4-amino) benzoylhydrazides as potential anti-hepatoma agents - ScienceDirect
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
Structure‐Activity‐Relationship‐Aided Design and Synthesis of xCT Antiporter Inhibitors - Cirillo - 2021 - ChemMedChem - Wiley Online Library
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
de por adulto (o preço varia de acordo com o tamanho do grupo)