Literature DB >> 24607578

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

Aparna Kadam1, Bhaskar Dawane1, Manisha Pawar1, Harshala Shegokar2, Kapil Patil2, Rohan Meshram2, Rajesh Gacche3.   

Abstract

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.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Carbothioamide derivatives; Goat lens aldose reductase; Paired potential analysis; Polyethylene glycol (PEG-400); Pyrazolone derivatives; Virtual screening

Mesh:

Substances:

Year:  2014        PMID: 24607578     DOI: 10.1016/j.bioorg.2014.02.002

Source DB:  PubMed          Journal:  Bioorg Chem        ISSN: 0045-2068            Impact factor:   5.275


  3 in total

Review 1.  Mitigating risk in academic preclinical drug discovery.

Authors:  Jayme L Dahlin; James Inglese; Michael A Walters
Journal:  Nat Rev Drug Discov       Date:  2015-04       Impact factor: 84.694

2.  Synthesis of α-substituted 2-(1H-1,2,4-triazol-3-yl)acetates and 5-amino-2,4-dihydro-3H-pyrazol-3-ones via the Pinner strategy.

Authors:  Dmytro M Khomenko; Roman O Doroshchuk; Hanna V Ivanova; Borys V Zakharchenko; Ilona V Raspertova; Oleksandr V Vaschenko; Sergiu Shova; Alexey V Dobrydnev; Yurii S Moroz; Oleksandr O Grygorenko; Rostyslav D Lampeka
Journal:  Tetrahedron Lett       Date:  2021-03-02       Impact factor: 2.032

Review 3.  Pyrazolone structural motif in medicinal chemistry: Retrospect and prospect.

Authors:  Zefeng Zhao; Xufen Dai; Chenyang Li; Xiao Wang; Jiale Tian; Ying Feng; Jing Xie; Cong Ma; Zhuang Nie; Peinan Fan; Mingcheng Qian; Xirui He; Shaoping Wu; Yongmin Zhang; Xiaohui Zheng
Journal:  Eur J Med Chem       Date:  2019-11-16       Impact factor: 6.514

  3 in total

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