Synthesis, single-crystal, in vitro antitumor evaluation and molecular docking of 3-substitued 5,5-diphenylimidazolidine-2,4-dione derivatives-Reference-Cited by-同舟云学术

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Synthesis, single-crystal, in vitro antitumor evaluation and molecular docking of 3-substitued 5,5-diphenylimidazolidine-2,4-dione derivatives

Published:2013-05-07 Issue:12 Volume:22 Page:6129-6142
ISSN:1054-2523
Container-title:Medicinal Chemistry Research
language:en
Short-container-title:Med Chem Res

Author:

Alanazi Amer M.,El-Azab Adel S.,Al-Swaidan Ibrahim A.,Maarouf Azza R.,El-Bendary Eman R.,Abu El-Enin Mohamed A.,Abdel-Aziz Alaa A.-M.

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Link

http://link.springer.com/content/pdf/10.1007/s00044-013-0597-1.pdf

Reference55 articles.

1. Abdel-Aziz AA-M (2007) Novel and versatile methodology for synthesis of cyclic imides and evaluation of their cytotoxic, DNA binding, apoptotic inducing activities and molecular modeling study. Eur J Med Chem 42:614–626

2. Abdel-Aziz AA-M, Al-Omar MA, El-Azab AS, Kunieda T (2010) Conformational preferences of sterically congested 2-imidazolidinone using X-ray analysis and computational studies. Part 1: Trans-1-acetyl-4,5-di-tert-butyl-2-imidazolidinone. J Mol Struct 969:145–154

3. Abdel-Aziz AA-M, ElTahir KEH, Asiri YA (2011) Synthesis, anti-inflammatory activity and COX-1/COX-2 inhibition of novel substituted cyclic imides. Part 1: molecular docking study. Eur J Med Chem 46:1648–1655

4. Abdel-Aziz AA-M, El-Azab AS, El-Subbagh HI, Al-Obaid AM, Alanazi AM, Al-Omar MA (2012) Design, synthesis, single-crystal and preliminary antitumor activity of novel arenesulfonylimidazolidin-2-ones. Bioorg Med Chem Lett 22:2008–2014

5. Al-Obaid AM, Abdel-Hamide SG, El-Kashef HA, Abdel-Aziz AA-M, El-Azab AS, Al-Khamees HA, El-Subbagh HI (2009) Substituted quinazolines, part 3. Synthesis, in vitro antitumor activity and molecular modeling study of certain 2-thieno-4(3H)-quinazolinone analogs. Eur J Med Chem 44:2379–2391

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