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Evaluation of inhibitory activity of few selected triazoles on xanthine oxidase - In silico studies
被引:1
|作者:
Louwkhyaa, V
[1
]
Babu, N. Yogi
[2
]
Das Manwal, Deva
[1
]
机构:
[1] Osmania Univ, Dept Chem, Hyderabad 500007, India
[2] Dr APJ Abdul Kalam Govt, Degree Coll, Dept Chem, Sanga Reddy 502319, Telangana State, India
来源:
关键词:
Febuxostat;
In silico Studies;
Inhibitory activity;
Selected triazoles;
Uric acid;
Xanthine Oxidase;
MOLECULAR-DYNAMICS SIMULATION;
DOCKING;
OXIDOREDUCTASE;
MECHANISM;
ENZYME;
DFT;
D O I:
10.56042/ijbb.v61i8.8515
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:
Hyperuricemia, also called Gout is a medical term used for joints pain associated with increased levels of uric acid in blood serum of a patient. The end product of purine metabolism in human body is uric acid. An enzyme called Xanthine Oxidase (XO) is a catalyst for this purine metabolism. Inhibitor which reduces the activity of an enzyme is used as a therapeutic agent to maintain the desired levels of uric acid in blood serum of patients. Such available inhibitors in the market include Febuxostat and Allopurinol which are widely used by Rheumatologists. The search for new molecules which can act as better inhibitor than the inhibitors presently available in the market is never ending. Eighteen various triazole (5 newly designed) compounds have been identified and their inhibitory activity(in silico) is evaluated on Xanthine Oxidase and it is found that all these triazoles show much better inhibitory activity on said enzyme, when compared to Febuxostat and Allopurinol.
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页码:485 / 496
页数:12
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