Biochemical Evaluation of Copper Compounds Derived from O- and N-/O- Donor Ligands

被引:3
|
作者
Akhtar, Muhammad Nadeem [1 ]
Shahid, Muhammad [2 ]
Sadakiyo, Masaaki [3 ]
Ikram, Muhammad [4 ]
Rehman, Sadia [4 ]
Ahmed, Irshad [5 ]
机构
[1] Univ Agr Faisalabad, Dept Chem, Faisalabad, Pakistan
[2] Univ Agr Faisalabad, Dept Biochem, Faisalabad, Pakistan
[3] Kyushu Univ, Int Inst Carbon Neutral Energy Res I2CNER, Nishi Ku, 744 Moto Oka, Fukuoka 8190395, Japan
[4] Abdul Wali Khan Univ, Dept Chem, Mardan, Pakistan
[5] Islamia Univ Bahawalpur, Dept Pharm, Bahawalpur, Pakistan
关键词
copper complexes; benzoate; 3-pyridinepropionic acid; antioxidant activity; alpha-enzyme inhibition; hemolytic activity; STRUCTURAL-CHARACTERIZATION; TRANSITION-METAL; BUTYRYLCHOLINESTERASE; ACETYLCHOLINESTERASE; INHIBITION; COMPLEXES; CHEMISTRY; UREASE;
D O I
10.1007/s11094-017-1596-1
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Compounds [Cu-II (2)(benz)(4)(Hbenz)(2)] (1) and [Cu-II(ppa)(2)(H2O)(2)] (n) (2), where benz = benzoate and ppa = 3-pyridinepropionic acid, were synthesized and studied for their 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging activity and the inhibition of enzymes such as acetylcholinesterase (AChE), butyrylcholinesterase (BChE), lipoxygenase (LOX), urease, chymotrypsin and alpha-glucosidase. The synthesized compounds were also studied by hemolytic method for their cytotoxicity and found to be low-toxicity substances. For AChE inhibition, compound 2 showed IC50 = 31.22 +/- 0.45 mu M, as compared to compound 1with IC50 = 36.52 +/- 0.44 mu M. Both compounds showed comparably low activity against BChE and were also active against urease, but compound 1 exhibited selective anti-urease activity. The anti-alpha-glucosidase activity of both compounds was comparable with that of standard drug used.
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页码:272 / 276
页数:5
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