Synthesis and pharmacological evaluation of pyrazolo[4,3-c]quinolinones as high affinity GABAA-R ligands and potential anxiolytics-Reference-Cited by-同舟云学术

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Synthesis and pharmacological evaluation of pyrazolo[4,3-c]quinolinones as high affinity GABAA-R ligands and potential anxiolytics

Published:2018-08 Issue:14 Volume:26 Page:3967-3974
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

López Rivilli Marisa J.,Turina Anahí V.,Bignante Elena A.,Molina Victor H.,Perillo María A.,Briñon Margarita C.,Moyano Elizabeth L.

Funder

CONICET

SECYT

Universidad Nacional de Córdoba

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference46 articles.

1. Microwave assisted solvent-free synthesis of pyrazolo[3,4-b]quinolines and pyrazolo[3,4-c]pyrazoles using p-TsOH

2. Synthesis and Antiviral Activities of New Pyrazolo[4,3‐c]quinolin‐3‐ones and Their Ribonucleoside Derivatives

3. Synthesis of 5H-Pyrazolo[4,3-c]quinolines

4. 2-Arylpyrazolo[4,3-c]quinolin-3-ones: a novel agonist, a partial agonist and an antagonist of benzodiazepines

5. Structure-activity relationship studies at benzodiazepine receptor (BZR): a comparison of the substituent effects of pyrazoloquinolinone analogs

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1. Anti-influenza virus activities and mechanism of antrafenine analogs;European Journal of Medicinal Chemistry;2023-11

2. Under or Absent Reporting of Light Stimuli in Testing of Anxiety-Like Behaviors in Rodents: The Need for Standardization;Frontiers in Molecular Neuroscience;2022-08-17

3. Design, Synthesis, Molecular Docking Analysis and Biological Evaluations of 4-[(Quinolin-4-yl)amino]benzamide Derivatives as Novel Anti-Influenza Virus Agents;International Journal of Molecular Sciences;2022-06-04

4. Current Approaches to the Search of Anxiolytic Drugs;Russian Journal of Bioorganic Chemistry;2021-05

5. Synthesis and structural characterization of nano‐sized metal complexes of 3‐(1‐methyl‐4‐hydroxy‐2‐oxo‐1,2‐dihydroquinolin‐3‐yl)‐2‐nitro‐3‐oxopropanoic acid. XRD, thermal, 3D modeling, and antitumor activity studies;Applied Organometallic Chemistry;2021-02-16

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