SYNTHESIS, CHARACTERIZATION, LIPOXYGENASE, AND TYROSINASE INHIBITORY ACTIVITIES OF NON-CYTOTOXIC TITANIUM(III) AND (IV) HYDRAZIDE COMPLEXES

被引:2
|
作者
Shaikh, Zara [1 ]
Ashiq, Uzma [1 ]
Jamal, Rifat Ara [2 ]
Gul, Sana [3 ]
Mahroof-Tahir, Mohammad [3 ]
Sultan, Sadaf [1 ]
Salar, Uzma [4 ]
Khan, Khalid Mohammed [5 ,6 ]
机构
[1] Univ Karachi, Dept Chem, Karachi 75270, Pakistan
[2] Fed Urdu Univ Art Sci & Technol, Dept Chem, Karachi, Pakistan
[3] Qatar Univ, Dept Chem & Earth Sci, Doha, Qatar
[4] Univ Karachi, Dr Panjwani Ctr Mol Med & Drug Res, Int Ctr Chem & Biol Sci, Karachi 75270, Pakistan
[5] Univ Karachi, HEJ Res Inst Chem, Int Ctr Chem & Biol Sci, Karachi 75270, Pakistan
[6] Imam Abdulrahman Bin Faisal Univ, Inst Res & Med Consultat IRMC, Dept Clin Pharm, POB 1982, Dammam 31441, Saudi Arabia
关键词
Titanium(III) and titanium(IV) hydrazide complex; Tyrosinase; Lipoxygenase; Inhibition; Molecular docking; Cytotoxicity; SODIUM DODECYL-SULFATE; ANTIOXIDANT PROPERTIES; POLYPHENOL OXIDASE; METAL-COMPLEXES; IN-VITRO; ACID; DERIVATIVES; LIGANDS; CYTOTOXICITY; EXPRESSION;
D O I
10.4314/bcse.v37i2.6
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ti(III) and (IV) hydrazide complexes were synthesized, characterized, and screened for their tyrosinase and lipoxygenase inhibitory and cytotoxic activities. The geometry of Ti(III) hydrazide complexes is tentatively assigned as octahedral. Magnetic moments were found around 1.7 B.M. and electronic spectral transition in the range of 495-518 nm. Evaluation of Ti(IV) and Ti(III) hydrazide complexes for tyrosinase and lipoxygenase inhibitory activities revealed varying inhibition potential. Hydrazide ligands were inactive against tyrosinase, while significant activity was observed against lipoxygenase (LOX). Good to moderate inhibition activity was observed by Ti(IV) and Ti(III) hydrazide complexes against both enzymes. At the same time, promising results were obtained for Ti(IV) hydrazide complexes against tyrosinase enzymes suggesting their broad application as tyrosinase inhibitors. Complex 4d possess negative inhibition, thus behaving as a tyrosinase activator. The docking results showed a good correlation between complex experimental activities and binding energies. Cytotoxic investigation revealed the non-toxicity of complexes against normal cells.
引用
收藏
页码:315 / 333
页数:19
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