Synthesis and anticancer evaluation of imidazolidine derivatives: study the reaction of imidazolidineiminothione derivatives with amino acids methyl ester

References

• Al-Harbi RAK, El-Sharief MAMS, Abbas SY. Synthesis and anticancer activity of bis-benzo[d][1,3]dioxol-5-yl thiourea derivatives with molecular docking study. Bioorg Chem. 2019;90:103088. doi: 10.1016/j.bioorg.2019.103088
   Web of Science ®Google Scholar
• Ammar YA, El-Sharief AMS, Belal A, et al. Design, synthesis, antiproliferative activity, molecular docking and cell cycle analysis of some novel (morpholinosulfonyl) isatins with potential EGFR inhibitory activity. Eur J Med Chem. 2018;156:918–932. doi: 10.1016/j.ejmech.2018.06.061
   PubMed Web of Science ®Google Scholar
• Shehry MF E, Ghorab MM, Abbas SY, et al. Quinoline derivatives bearing pyrazole moiety: synthesis and biological evaluation as possible antibacterial and antifungal agents. Eur J Med Chem. 2018;143:1463–1473. doi: 10.1016/j.ejmech.2017.10.046
   Web of Science ®Google Scholar
• Abbas SY, Zhao P, Overman L. 1,6-Addition of tertiary carbon radicals generated from alcohols or carboxylic acids by visible-light photoredox catalysis. Org Lett. 2018;20(3):868–871. doi: 10.1021/acs.orglett.7b04034
   PubMed Web of Science ®Google Scholar
• Abbas SY, El–Bayouki KAM, Basyouni WM. Utilization of isatoic anhydride in the syntheses of various types of quinazoline and quinazolinone derivatives. Synthetic Commun. 2016;46(12):993–1035. doi: 10.1080/00397911.2016.1177087
   Web of Science ®Google Scholar
• Gao Z, Duhl DD, Harrison SD. Chapter 20. Beyond kinases: Purine-binding enzymes as cancer targets. Ann Rep Med Chem. 2003;38:193–202.
   Web of Science ®Google Scholar
• Trunz BB, Jedrysiak R, Tweats D, et al. 1- Aryl-4-Nitro-1H-imidazoles, a new promising series for the treatment of human African Trypanosomiasis. Eur J Med Chem. 2011;46:1524–1535. doi: 10.1016/j.ejmech.2011.01.071
   PubMed Web of Science ®Google Scholar
• Bascou JP, Lacroix G, Gadras A, et al. Derives optiquement actifs de 2-imidazoline-5-one et 2-imidazoline-5-thiones fungicide. E P Patent 1994; 0 629616 A2.
   Google Scholar
• Odake S, Morikava T, Tsuchiya M, et al. Inhibition of helicobacter pylori urease activity by hydroxamicp acid derivatives. Biol Pharm Bull. 1994;17:1329–1332. doi: 10.1248/bpb.17.1329
   PubMed Web of Science ®Google Scholar
• Kassouf W, Tanguay S, Aprikian A. Nilutamide as second line hormone therapy for prostate cancer after androgen ablation fails. G J Urol. 2003;169:1742–1744. doi: 10.1097/01.ju.0000057795.97626.66
   Google Scholar
• Abbas SY, El-Sharief MAMS, Al-Harbi RAK, et al. Synthesis and evaluation of 5-imino-4-thioxoimidazolidin-2-one derivatives as antibacterial and antifungal agents. Med Chem. 2020; doi:10.2174/1573406416666191227112648.
   Google Scholar
• El-Sharief MAMS, Abbas SY, El-Sharief AMS, et al. 5-Thioxoimidazolidine-2- one derivatives: synthesis, anti-Inflammatory activity, Analgesic activity, COX Inhibition assay and molecular Modelling study. Bioorg Chem. 2019;87:679–687. doi: 10.1016/j.bioorg.2019.03.075
   PubMed Web of Science ®Google Scholar
• Moussa Z, El-Sharief MAMS, Abbas SY. New imidazolidineiminothione derivatives: synthesis, spectral Characterization and evaluation of antitumor, antiviral, antibacterial and antifungal activities. Eur J Med Chem. 2016;122:419–428. doi: 10.1016/j.ejmech.2016.06.051
   PubMed Web of Science ®Google Scholar
• El-Sharief MMS, Abbas SY, Moussa Z, et al. Synthesis and evaluation of antibacterial and antifungal activities of 1,3-Disubstituted-4- Thioxoimidazolidin-2-One derivatives. Croat Chem Acta. 2018;91(3):335–340. doi: 10.5562/cca3354
   Web of Science ®Google Scholar
• Iijima S. Helical microtubules of graphitic carbon. Nature. 1991;354:56–58. doi: 10.1038/354056a0
   Web of Science ®Google Scholar
• Kijima T., (Ed.) Inorganic and Metallic nanotubular materials. Top Appl Phys. 2010;117:17–32. doi: 10.1007/978-3-642-03622-4_2
   Google Scholar
• Gong D, Grimes CA, Varghese OK, et al. Titanium oxide nanotube arrays prepared by anodic oxidation. J Mater Res. 2001;16:3331–3334. doi: 10.1557/JMR.2001.0457
   Web of Science ®Google Scholar
• Nakamura H, Matsui Y. Silica Gel nanotubes obtained by the Sol-Gel method. J Am Chem Soc. 1995;117(9):2651–2652. doi: 10.1021/ja00114a031
   Web of Science ®Google Scholar
• Linsebigler AL, Lu G, Yates JT. Photocatalysis on TiO2 surfaces: Principles, mechanisms, and selected Results. Chem Rev. 1995;95:735–758. doi: 10.1021/cr00035a013
   Web of Science ®Google Scholar
• Fujishima A, Hondam K. Electrochemical photolysis of water at a semiconductor electrode. Nature. 1972;238:37–38. doi: 10.1038/238037a0
   PubMed Web of Science ®Google Scholar
• Abbas SY, El-Sharief MAMS, Salem MA, et al. Utilization of cyanothioformamides in the syntheses of various types of imidazole derivatives. Synthetic Commun. 2020;50:621–648. doi: 10.1080/00397911.2019.1700524
   Web of Science ®Google Scholar
• Qu XF, Yuan J, Deng X, et al. An efficient method to Form TiO2/CdS nanotube Arrays using Anodic Aluminum oxide (AAO) templates. Key Eng Mater. 2016;727:374–380. doi: 10.4028/www.scientific.net/KEM.727.374
   Google Scholar
• Skehan P, Storeng R, Scudiero D, et al. New colorimetric cytotoxicity assay for anticancer-drug screening. J Natl Cancer Inst. 1990;82:1107–1112. doi: 10.1093/jnci/82.13.1107
   PubMed Web of Science ®Google Scholar
• Kustiningsih I, Purwanto WW. Synthesis of Titania nanotubes and Titania nanowires by combination sonication-hydrothermal treatment and their photocatalytic activity for hydrogen production. Int J Technol. 2014;5(2):133. doi: 10.14716/ijtech.v5i2.400
   Google Scholar