Synthesis, benzodiazepine receptor binding and molecular modelling of isochromeno[4,3-c]pyrazol-5(1H)-one derivatives-Reference-Cited by-同舟云学术

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Synthesis, benzodiazepine receptor binding and molecular modelling of isochromeno[4,3-c]pyrazol-5(1H)-one derivatives

Published:2012-08 Issue: Volume:54 Page:709-720
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Maggio B.,Raffa D.,Raimondi M.V.,Plescia F.,Trincavelli M.L.,Martini C.,Meneghetti F.,Basile L.,Guccione S.,Daidone G.

Funder

MURST

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference28 articles.

1. Mapping of the Benzodiazepine Recognition Site on GABA-A Receptors

2. GABAA Receptor Structure–Function Studies: A Reexamination in Light of New Acetylcholine Receptor Structures

3. Molecular models for recognition and activation at the benzodiazepine receptor: A review

4. Consecutive Pschorr–Sandmeyer reactions in a pyrazole series. Part 2.1 Access to the [2]benzopyrano[4,3-c]pyrazole system of pharmaceutical interest

5. Studies on the synthesis of heterocyclic compounds. Part IV. Further investigation of the pschorr reaction with some pyrazole derivatives

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5. A facile and metal-free domino reaction of TsDAM and 2-alkenylarylaldehyde: An easy access to 8-hydroxy-2,8-dihydro indeno [2,1-c]pyrazoles;Organic & Biomolecular Chemistry;2021

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