Thiohydantoin derivatives incorporating a pyrazole core: Design, synthesis and biological evaluation as dual inhibitors of topoisomerase-I and cycloxygenase-2 with anti-cancer and anti-inflammatory activities
- 1 October 2019
- journal article
- research article
- Published by Elsevier in Bioorganic Chemistry
- Vol. 91, 103132
Abstract
No abstract availableKeywords
Funding Information
- Beni-Suef University, Egypt
This publication has 31 references indexed in Scilit:
- OSU-A9 inhibits angiogenesis in human umbilical vein endothelial cells via disrupting Akt–NF-κB and MAPK signaling pathwaysToxicology and Applied Pharmacology, 2013
- The novel benzopyran class of selective cyclooxygenase-2 inhibitors. Part 2: The second clinical candidate having a shorter and favorable human half-lifeBioorganic & Medicinal Chemistry Letters, 2010
- Synthesis of new pyrazole derivatives and their anticancer evaluationEuropean Journal of Medicinal Chemistry, 2010
- Promise and challenges in drug discovery and development of hybrid anticancer drugsExpert Opinion on Drug Discovery, 2009
- Pro-Inflammatory Enzymes, Cyclooxygenase 1, Cyclooxygenase 2, and 5-Lipooxygenase, Inhibited by Stabilized Rice Bran ExtractsJournal of Medicinal Food, 2009
- Topoisomerase I inhibitors: camptothecins and beyondNature Reviews Cancer, 2006
- Anticancer effect of three pyrazole derivativesNatural Product Research, 2006
- Celecoxib Inhibits Prostate Cancer Growth: Evidence of a Cyclooxygenase-2-Independent MechanismClinical Cancer Research, 2005
- Cellular roles of DNA topoisomerases: a molecular perspectiveNature Reviews Molecular Cell Biology, 2002
- DNA Topoisomerases: Structure, Function, and MechanismAnnual Review of Biochemistry, 2001