Development of novel pyrazolone derivatives as inhibitors of aldose reductase: An eco-friendly one-pot synthesis, experimental screening and in silico analysis

被引:29
作者
Kadam, Aparna [1 ]
Dawane, Bhaskar [1 ]
Pawar, Manisha [1 ]
Shegokar, Harshala [2 ]
Patil, Kapil [2 ]
Meshram, Rohan [2 ]
Gacche, Rajesh [2 ]
机构
[1] Swami Ramanand Teerth Marathwada Univ, Sch Chem Sci, Nanded, MS, India
[2] Swami Ramanand Teerth Marathwada Univ, Sch Life Sci, Nanded, MS, India
关键词
Goat lens aldose reductase; Pyrazolone derivatives; Carbothioamide derivatives; Polyethylene glycol (PEG-400); Paired potential analysis; Virtual screening; UNIVERSAL FORCE-FIELD; EFFICIENT; BINDING; SITE; NEUROPATHY; TUMOR;
D O I
10.1016/j.bioorg.2014.02.002
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
Aldose reductase is the key enzyme of polypol pathway leading to accumulation of sorbitol. Sorbitol does not diffuse across the cell membranes easily and therefore accumulates within the cell, causing osmotic damage which leads to retinopathy (cataractogenesis), neuropathy and other diabetic complications. Currently, aldose reductase inhibitors like epalrestat, ranirestat and fidarestat are used for the amelioration of diabetic complications. However, such drugs are effective in patients having good glycemic control and less severe diabetic complications. In present study we have designed novel pyrazolone derivative and performed eco-friendly synthesis approach and tested the synthesized compounds as potential inhibitors of aldose reductase activity. Additional in silico analysis in current study indicates presence of highly conserved chemical environment in active site of goat lens aldose reductase. The reported data is expected to be useful for developing novel pyrazolone derivatives as lead compounds in the management of diabetic complications. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:67 / 74
页数:8
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