Skip to main content
Log in

Antioxidative and antitumour properties of metal(II) solid complexes with 8-acetyl-4-methyl umbelliferone

  • Published:
Transition Metal Chemistry Aims and scope Submit manuscript

Abstract

Six transition metal(II) complexes with 8-acetyl-4-methyl umbelliferone (AMUH), ML2 (L = AMU; M = Mn, Co, Ni, Cu, Zn and Cd), have been synthesized and characterized by elemental analysis, electrical conductance, i.r., 1H-n.m.r. and u.v. spectroscopic techniques. The e.s.r. spectra show that CuL2 is anisotropic, with g ⊥ ≈ 2.05 and g≈2.26. The MnL2 species is characterized by a very broad g≈2 centered resonance without manganese hyperfine structure. The antioxidative and other biological activities of selected complexes were also investigated, indicating that both the ligand and complexes exhibit a scavenging effect on the superoxide radical (O2 −·) and a suppressing effect on the hydroxyl radical (·OH). The suppressing effect on ·OH is greater than the scavenging effect on O2 ·. The Cu and Mn complexes exhibit very significant suppression ratios for both radicals. However, the inhibitory effect on lipid peroxides results show that, in the initial stage, the Cu and Mn complexes exhibit obvious inhibitory effects on lipid peroxides, but after one hour, they begin to accelerate the lipid peroxides. Lower catalytic activity and instability when the complexes react with active oxygen may be responsible for this dual nature. The ligand and four transition metal(II) complexes selectively, obviously, inhibit the growth of HCT-8 and HL-60 tumour cell lines. They also exhibit a minor influence on the proliferation of B cells in higher concentration (10−5 m), but only a weak effect on the proliferation of T cells of the BALB/C (nude rate) spleen cells.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. B. Halliwell and J.M. Gutteridge, Methods in Enzymology, 186, 1 (1990).

    Google Scholar 

  2. S.J. Stohs and D. Bagchi, Free Radical Biology and Medicine, 18, 321 (1995).

    Google Scholar 

  3. W.K. Pogozelski and T.D. Tullius, Chem. Rev., 98, 1089 (1998).

    Google Scholar 

  4. R.M. Burger, Chem. Rev., 98, 1153 (1998).

    Google Scholar 

  5. C.J. Burrows and J.G. Muller, Chem. Rev., 98, 1109 (1998).

    Google Scholar 

  6. D. Schmahl, Carcinogenicity of Anticancer Drugs and especially Alkylating Agents, in Carcinogenicity of Alkylating Cytostatic Drugs, D. Schmahl and J.M. Kdldor (Eds.), IARC Scientific Publications No. 78, International Agency for Research on Cancer, Lyon, 1986, pp. 29-36.

    Google Scholar 

  7. R.B. Arora and C.N. Mathur, Brit. J. Pharmacol., 20, 29 (1963).

    Google Scholar 

  8. C.R. Hancock, H.W.B. Barlow and H.J. Lacey, J. Exptl. Botany, 12, 401 (1961).

    Google Scholar 

  9. S. Lehnet, G. Fisher and G. Methot, Int. J. Radiat. Biol., 40, 63 (1981).

    Google Scholar 

  10. Z.S. Tong, M.X. Huang and C.S. Dai, Chinese J. Med. Chem., 4, 150 (1994).

    Google Scholar 

  11. V.J.T. Raju, V. Ranbaore, V. Atre and M.C. Ganorkar, J. Indian Chem. Soc., LIX, 199 (1982).

    Google Scholar 

  12. P. Singh, V. Singh, R.L. Goel and B.P. Singh, J. Indian Chem. Soc., LII, 958 (1975).

    Google Scholar 

  13. M.N. Hughes, The Inorganic Chemistry of Biological Processes, Wiley Interscience, London, 1972.

    Google Scholar 

  14. L.M. Mosmmann, J. Immuno. Meth., 65, 55 (1983).

    Google Scholar 

  15. V. Ponti, M.V. Dianzani, K.J. Cheeseman and T.F. Stater, Chem. Biol. Interact, 23, 281 (1978).

    Google Scholar 

  16. B. Halliwell and J.M.C. Gutteridge, Febs Letters, 128, 347 (1981).

    Google Scholar 

  17. E. Niki, E. Komuro, M. Takahashi, S. Urano, E. Ito and K. Terao, J. Biol. Chem., 263, 19809 (1988).

    Google Scholar 

  18. D.R. Davies and G.A. Webb, Coord. Chem. Rev., 6, 95 (1971).

    Google Scholar 

  19. K. Nakamoto, Infrared and Raman Spectra of Inorganic and Coordination Compounds, 3rd Edit., Wiley Interscience, New York, 1978.

    Google Scholar 

  20. Q. Zhang, L.F. Wang, X. Liu, S.B. Li and F.Y. He, Transition Met. Chem., 21, 23 (1996).

    Google Scholar 

  21. T. Minegishi, T. Hoshi and Y. Tanizaki, Nippon Kagaku Kaishi, 649 (1978).

  22. B. Mabad, P. Cassoux, J.P. Tuchagues and D.N. Hendrickson, Inorg. Chem., 25, 1420 (1986).

    Google Scholar 

  23. R.D. Dowsing, J.F. Gibson, M. Goodgame and P.J. Hayward, J. Chem. Soc. A, 187 (1969).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zhang, Q., Zhai, JJ., Zhang, YR. et al. Antioxidative and antitumour properties of metal(II) solid complexes with 8-acetyl-4-methyl umbelliferone. Transition Metal Chemistry 25, 93–98 (2000). https://doi.org/10.1023/A:1007036718734

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1007036718734

Keywords

Navigation