Copper Complexes of Nicotinic-Aromatic Carboxylic Acids as Superoxide Dismutase Mimetics

被引:85
作者
Suksrichavalit, Thummaruk [1 ]
Prachayasittikul, Supaluk [2 ]
Piacham, Theeraphon [1 ]
Isarankura-Na-Ayudhya, Chartchalerm [1 ]
Nantasenamat, Chanin [1 ]
Prachayasittikul, Virapong [1 ]
机构
[1] Mahidol Univ, Fac Med Technol, Dept Clin Microbiol, Bangkok 10700, Thailand
[2] Srinakharinwirot Univ, Fac Sci, Dept Chem, Bangkok 10110, Thailand
来源
MOLECULES | 2008年 / 13卷 / 12期
关键词
Nicotinic acid; Copper; Carboxylic acid; Superoxide dismutase; Antimicrobial activity;
D O I
10.3390/molecules13123040
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nicotinic acid (also known as vitamin B3) is a dietary element essential for physiological and antihyperlipidemic functions. This study reports the synthesis of novel mixed ligand complexes of copper with nicotinic and other select carboxylic acids (phthalic, salicylic and anthranilic acids). The tested copper complexes exhibited superoxide dismutase (SOD) mimetic activity and antimicrobial activity against Bacillus subtilis ATCC 6633, with a minimum inhibition concentration of 256 mu g/mL. Copper complex of nicotinic-phthalic acids (CuNA/Ph) was the most potent with a SOD mimetic activity of IC50 34.42 mu M. The SOD activities were observed to correlate well with the theoretical parameters as calculated using density functional theory (DFT) at the B3LYP/LANL2DZ level of theory. Interestingly, the SOD activity of the copper complex CuNA/Ph was positively correlated with the electron affinity (EA) value. The two quantum chemical parameters, highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO), were shown to be appropriate for understanding the mechanism of the metal complexes as their calculated energies show good correlation with the SOD activity. Moreover, copper complex with the highest SOD activity were shown to possess the lowest HOMO energy. These findings demonstrate a great potential for the development of value-added metallovitamin-based therapeutics.
引用
收藏
页码:3040 / 3056
页数:17
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