Systhesis and Spectroscopic Properties of Curcumin Analogues Combined with Chlorine

Article Preview

Abstract:

Three curcumin analogues were synthesized from 4-chlorobenzaldehyde and cyclohexanone,cyclopentane and aceton,and their spectroscopic properties were determined. The synthetics had the structural properties such as the target compounds,which showed their particular spectroscopic properties.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 554-556)

Pages:

1919-1924

Citation:

Online since:

July 2012

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2012 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] B. B. Aggarwal, K. B. Harikumar, Int. J. Biochem. Cell Bio,Vol. 41(2008), pp.40-59

Google Scholar

[2] R. Kuttan, P. Bhanumathy, K. Nirmala,et al. Cancer. Lett,Vol. 29(1985), pp.197-202

Google Scholar

[3] L. G. Menon, R. Kuttan, G. Kuttan,et al. Cancer.Lett,Vol.95(1995), pp.221-225

Google Scholar

[4] Y. S. Chen, C. C. Ho, K. C. Cheng, et al. Toxicol InVitro,Vol.17(2003), pp.323-333

Google Scholar

[5] J. H. Woo, Y. H. Kim, Y. J. Choi, et al. Cancer Biology,Vol.24(2003), pp.1139-1281

Google Scholar

[6] J.Ushida, S.Sugie, K.Kawabata,etal. Cancer Res, Vol.9 (2000): pp.893-898

Google Scholar

[7] T. Kawamori, R. Lubet, V. E. Steele, et al. Cancer. Res., Vol.59(1999), pp.597-601

Google Scholar

[8] T. Masuda, K. Hidaka, A. Shinohara, et al. Agric. Food Chem., Vol. 47(1999), pp.71-77

Google Scholar

[9] P. Anand, A.B. Kunnumakkara, R.A. Newman, et al. Mol Pharm. Vol. 4 (2007), pp.807-818

Google Scholar

[10] E. R. Hahm, Y. S. Gho, Park S., et al. Biochemical and Biophysical Research Communications, Vol.321(2004), pp.337-344

Google Scholar

[11] E. M. Al-Hujaily, A. G. Mohamed, I. Al-Sharif. Breast Cancer Res. Treat.,Vol.128(2010), pp.97-107

Google Scholar

[12] J. Ishida, H. Ohtsu, Y. Tachibana, et al. Bioorg. Med. Chem.,Vol.10(2002), p.3481–3487

Google Scholar

[13] K. D. Shiv, K. S. Anuj, N. Upma, et al. European Journal of Medicinal Chemistry, Vol.43(2008), pp.1837-1846

Google Scholar

[14] C. M. Ahn, B. Park, H. B. Woo, et al. Bioorganic & Medicinal Chemistry Letters, Vol.19(2009), pp.1483-1491

Google Scholar

[15] P. Lu, Q. Tong, F. Jiang, et al. Huazhong Univ. Sci. Technol. Med. Sci., Vol.25(2005), p.668–670

Google Scholar

[16] M. Pisano, G.Pagnan, M. A. Dettori,et al. Mol. Cancer, Vol.9(2010), pp.137-148

Google Scholar

[17] L. Lin, B. Hutzen, S. Ball, et al. Cancer science, Vol.100(2009), pp.1719-1727

Google Scholar

[18] S. Daniele, R. Michele, R. Riccardo, et al. Bioorganic & Medicinal Chemistry Letters, Vol.18(2008), p.845–849

Google Scholar

[19] W. M. Weber, L. A. Hunsaker, C. N. Roybal, et al. Bioorg. Med. Chem.,Vol.14(2006), p.2450–2461

Google Scholar

[20] G. Liang, L. Shao, Y Wang., et al. Bioorganic & Medicinal Chemistry, Vol.17(2009), p.2623–2631

Google Scholar

[21] A. P. Zambre, V. M. Kulkarni, S. Padhye, et al. Bioorg. Med. Chem., Vol.14(2006), pp.7196-7204

Google Scholar

[22] L. Lin, Q. Shi, A. K. Nyarko, et al. Med. Chem., Vol.49(2006), p.3963–3972

Google Scholar

[23] D. Youssef, C. E. Nichols, T. S. Cameron, et al. Bioorganic & Medicinal Chemistry Letters, Vol.17(2007), p.5624–5629

Google Scholar