Syntheses, characterization and biological activities of rare earth metal complexes with curcumin and 1,10-phenanthroline-5,6-dione

作者: Yu-Min Song , Jun-Peng Xu , Lan Ding , Qian Hou , Jing-Wang Liu

DOI: 10.1016/J.JINORGBIO.2008.12.001

关键词: MetalRadicalMolar conductivityPolymer chemistryChemistryDeprotonationStereochemistryAntibacterial activityDenticityLigandPhenanthroline

摘要: Abstract Three new solid complexes have been synthesized by the reaction of rare earth(III) nitrate with first ligand curcumin (HL) and second 1,10-phenanthroline-5,6-dione (L′) in alcohol solution (pH = 6.5–7.0). The composition has characterized elemental analysis, molar conductivity, thermogravimetric IR, UV–vis methods. results reveal that β-diketone group to coordinates earth ions bidentate mode after deprotonated. But uses its two N atoms mode. general formula is REL 3 L′ (RE = Sm, Eu, Dy). antibacterial activity indicated excellent ability for testing bacterium than curcumin. result agarose gel electrophoresis suggested complex SmL can cleave plasmid DNA at physiological pH temperature. And it was found cleavage process sensitive pH, however, adding radical scavengers almost had no effect on reaction, therefore, does not produce diffusible hydroxyl radicals via Fenton reaction.

参考文章(19)
K.K. Sharma, S. Chandra, D.K. Basu, Synthesis and antiarthritic study of a new orally active diferuloyl methane (curcumin) gold complex Inorganica Chimica Acta. ,vol. 135, pp. 47- 48 ,(1987) , 10.1016/S0020-1693(00)83260-0
S. Satyanarayana, James C. Dabrowiak, Jonathan B. Chaires, Neither delta- nor lambda-tris(phenanthroline)ruthenium(II) binds to DNA by classical intercalation. Biochemistry. ,vol. 31, pp. 9319- 9324 ,(1992) , 10.1021/BI00154A001
K. Krishnankutty, V. D. John, Synthesis, Characterization, and Antitumour Studies of Metal Chelates of Some Synthetic Curcuminoids Synthesis and Reactivity in Inorganic and Metal-organic Chemistry. ,vol. 33, pp. 343- 358 ,(2003) , 10.1081/SIM-120017791
Marco Borsari, Erika Ferrari, Romano Grandi, Monica Saladini, Curcuminoids as potential new iron-chelating agents: spectroscopic, polarographic and potentiometric study on their Fe(III) complexing ability Inorganica Chimica Acta. ,vol. 328, pp. 61- 68 ,(2002) , 10.1016/S0020-1693(01)00687-9
A. Arrieta, F. Dietze, G. Mann, L. Beyer, J. Hartung, Säurestärke und Komplexbildung von Curcuminoiden Journal Fur Praktische Chemie-chemiker-zeitung. ,vol. 330, pp. 111- 118 ,(1988) , 10.1002/PRAC.19883300120
Khosro Mohammadi, Katherine H. Thompson, Brian O. Patrick, Tim Storr, Candice Martins, Elena Polishchuk, Violet G. Yuen, John H. McNeill, Chris Orvig, Synthesis and characterization of dual function vanadyl, gallium and indium curcumin complexes for medicinal applications. Journal of Inorganic Biochemistry. ,vol. 99, pp. 2217- 2225 ,(2005) , 10.1016/J.JINORGBIO.2005.08.001
Jean-Claude G. Bünzli, Steve Comby, Anne-Sophie Chauvin, Caroline D.B. Vandevyver, New Opportunities for Lanthanide Luminescence Journal of Rare Earths. ,vol. 25, pp. 257- 274 ,(2007) , 10.1016/S1002-0721(07)60420-7
K. Krishnankutty, P. Venugopalan, Metal Chelates of Curcuminoids Synthesis and Reactivity in Inorganic and Metal-organic Chemistry. ,vol. 28, pp. 1313- 1325 ,(1998) , 10.1080/00945719809349407
Kapil Mehta, Panayotis Pantazis, Theresa McQueen, Bharat B Aggarwal, ANTIPROLIFERATIVE EFFECT OF CURCUMIN (DIFERULOYLMETHANE) AGAINST HUMAN BREAST TUMOR CELL LINES Anti-Cancer Drugs. ,vol. 8, pp. 470- 481 ,(1997) , 10.1097/00001813-199706000-00010