2,2′-Dihydroxybenzophenones and their carbonyl N-analogues as inhibitor scaffolds for MDR-involved human glutathione transferase isoenzyme A1-1-Reference-Cited by-同舟云学术

2,2′-Dihydroxybenzophenones and their carbonyl N-analogues as inhibitor scaffolds for MDR-involved human glutathione transferase isoenzyme A1-1

Published:2014-08 Issue:15 Volume:22 Page:3957-3970
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Perperopoulou Fereniki D.,Tsoungas Petros G.,Thireou Trias N.,Rinotas Vagelis E.,Douni Eleni K.,Eliopoulos Elias E.,Labrou Nikolaos E.,Clonis Yannis D.

Publisher

Elsevier BV

Subject

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

Reference47 articles.

1. Polyisoprenylated Benzophenones from Clusiaceae: Potential Drugs and Lead Compounds

2. Naphthylphenstatins as tubulin ligands: Synthesis and biological evaluation

3. Electron-Deficient Dienes. 5. An Inverse-Electron-Demand Diels−Alder Approach to 2-Substituted 4-Methoxyxanthones and 3,4-Dimethoxyxanthones

4. Domino Reaction to Functionalized 2-Hydroxybenzophenones from Electron-Deficient Chromones and 1,3-Dicarbonyl Compounds

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