About this Journal Submit a Manuscript Table of Contents
BioMed Research International
Volume 2013 (2013), Article ID 207181, 7 pages
http://dx.doi.org/10.1155/2013/207181
Research Article

Synthesis of Novel Compounds as New Potent Tyrosinase Inhibitors

Department of Chemistry, Payame Noor University (PNU), P.O. Box 19395-3697, Tehran, Iran

Received 1 July 2013; Accepted 5 September 2013

Academic Editor: Hirotaka Iwase

Copyright © 2013 Hooshang Hamidian. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. H.-S. Lee, “Tyrosinase inhibitors of Pulsatilla cernua root-derived materials,” Journal of Agricultural and Food Chemistry, vol. 50, no. 6, pp. 1400–1403, 2002. View at Publisher · View at Google Scholar · View at Scopus
  2. Y. Masamoto, H. Ando, Y. Murata, Y. Shimoishi, M. Tada, and K. Takahata, “Mushroom tyrosinase inhibitory activity of esculetin isolated from seeds of Euphorbia lathyris L,” Bioscience, Biotechnology and Biochemistry, vol. 67, no. 3, pp. 631–634, 2003. View at Scopus
  3. P. B. Bandgar, L. K. Adsul, H. V. Chavan et al., “Synthesis, biological evaluation, and molecular docking of N-{3-[3-(9-methyl-9H-carbazol-3-yl)-acryloyl]-phenyl}-benzamide/amide derivatives as xanthine oxidase and tyrosinase inhibitors,” Bioorganic and Medicinal Chemistry, vol. 20, no. 18, pp. 5649–5657, 2012.
  4. J. C. Cho, H. S. Rho, Y. H. Joo et al., “Depigmenting activities of kojic acid derivatives without tyrosinase inhibitory activities,” Bioorganic and Medicinal Chemistry Letters, vol. 22, no. 12, pp. 4159–4162, 2012.
  5. U. Ghani and N. Ullah, “New potent inhibitors of tyrosinase: novel clues to binding of 1,3,4-thiadiazole-2(3H)-thiones, 1,3,4-oxadiazole-2(3H)-thiones, 4-amino-1,2,4-triazole-5(4H)-thiones, and substituted hydrazides to the dicopper active site,” Bioorganic and Medicinal Chemistry, vol. 18, no. 11, pp. 4042–4048, 2010. View at Publisher · View at Google Scholar · View at Scopus
  6. I. M. A. Awad, A. H. Osman, and A. A. M. Aly, “Heterocyclo-substituted sulfa drugs: part XII. Mercapto-S-azo-benzothiazol dyes and their metal complexes,” Phosphorus, Sulfur and Silicon and the Related Elements, vol. 178, no. 6, pp. 1339–1352, 2003. View at Publisher · View at Google Scholar · View at Scopus
  7. B. Akkurt and E. Hamuryudan, “Enhancement of solubility via esterification: synthesis and characterization of octakis (ester)-substituted phthalocyanines,” Dyes and Pigments, vol. 79, no. 2, pp. 153–158, 2008. View at Publisher · View at Google Scholar · View at Scopus
  8. A. M. Sevim, S. Arkan, A. Koca, and A. Gül, “Synthesis and spectroelectrochemistry of new phthalocyanines with ester functionalities,” Dyes and Pigments, vol. 92, no. 3, pp. 1114–1121, 2012. View at Publisher · View at Google Scholar · View at Scopus
  9. H. Khanmohammadi and M. Darvishpour, “New azo ligands containing azomethine groups in the pyridazine-based chain: aynthesis and characterization,” Dyes and Pigments, vol. 81, no. 3, pp. 167–173, 2009. View at Publisher · View at Google Scholar · View at Scopus
  10. A. Z. Al-Rubaie, A. A. Al-Fregi, and S. A. S. Al-Jadaan, “Synthesis of a new series of 2-(2-hydroxynaphthylazo)aryltellurium compounds,” Phosphorus, Sulfur and Silicon and the Related Elements, vol. 186, no. 1, pp. 115–124, 2011. View at Publisher · View at Google Scholar · View at Scopus
  11. M. M. M. Raposo, A. M. R. C. Sousa, A. M. C. Fonseca, and G. Kirsch, “Thienylpyrrole azo dyes: synthesis, solvatochromic and electrochemical properties,” Tetrahedron, vol. 61, no. 34, pp. 8249–8256, 2005. View at Publisher · View at Google Scholar · View at Scopus
  12. F. Karci, A. Demirçali, I. Şener, and T. Tilki, “Synthesis of 4-amino-1H-benzo[4,5]imidazo[1,2-H]pyrimidin-2-one and its disperse azo dyes. Part 1: phenylazo derivatives,” Dyes and Pigments, vol. 71, no. 2, pp. 90–96, 2006. View at Publisher · View at Google Scholar · View at Scopus
  13. M. R. Yazdanbakhsh, A. Ghanadzadeh, and E. Moradi, “Synthesis of some new azo dyes derived from 4-hydroxy coumarin and spectrometric determination of their acidic dissociation constants,” Journal of Molecular Liquids, vol. 136, no. 1-2, pp. 165–168, 2007. View at Publisher · View at Google Scholar · View at Scopus
  14. H. Zeng, Z. P. Lin, and A. C. Sartorelli, “Resistance to purine and pyrimidine nucleoside and nucleobase analogs by the human MDR1 transfected murine leukemia cell line L1210/VMDRC.06,” Biochemical Pharmacology, vol. 68, no. 5, pp. 911–921, 2004. View at Publisher · View at Google Scholar · View at Scopus
  15. P. Sharma, N. Rane, and V. K. Gurram, “Synthesis and QSAR studies of pyrimido[4,5-d]pyrimidine-2,5-dione derivatives as potential antimicrobial agents,” Bioorganic and Medicinal Chemistry Letters, vol. 14, no. 16, pp. 4185–4190, 2004. View at Publisher · View at Google Scholar · View at Scopus
  16. C. Q. Huang, K. M. Wilcoxen, D. E. Grigoriadis, J. R. McCarthy, and C. Chen, “Design and synthesis of 3-(2-pyridyl)pyrazolo[1,5-a]pyrimidines as potent CRF1 receptor antagonists,” Bioorganic and Medicinal Chemistry Letters, vol. 14, no. 15, pp. 3943–3947, 2004. View at Publisher · View at Google Scholar · View at Scopus
  17. M. F. Abdel-Megeed, B. E. Badr, M. M. Azaam, and G. A. El-Hiti, “Antimicrobial activities of a series of diphenyl(arylamino)(1-phenyl-3-(pyridin-2-Yl)-1H-pyrazol-4-Yl)methylphosphonates phosphorus,” Phosphorus, Sulfur, and Silicon and the Related Elements, vol. 187, no. 10, pp. 1202–1207, 2012.
  18. H. Hamidian, R. Tagizadeh, S. Fozooni, V. Abbasalipour, A. Taheri, and M. Namjou, “Synthesis of novel azo compounds containing 5(4H)-oxazolone ring as potent tyrosinase inhibitors,” Bioorganic and Medicinal Chemistry, vol. 21, no. 7, pp. 2088–2092, 2013.
  19. H.-M. Wang, C.-Y. Chen, C.-Y. Chen et al., “(-)-N-Formylanonaine from Michelia alba as a human tyrosinase inhibitor and antioxidant,” Bioorganic and Medicinal Chemistry, vol. 18, no. 14, pp. 5241–5247, 2010. View at Publisher · View at Google Scholar · View at Scopus
  20. J. Han, I. Ma, M. J. Hendzel, and J. Allalunis-Turner, “The cytotoxicity of γ-secretase inhibitor I to breast cancer cells is mediated by proteasome inhibition, not by γ-secretase inhibition,” Breast Cancer Research, vol. 11, no. 4, article R57, 2009. View at Publisher · View at Google Scholar · View at Scopus