Concise perspectives on some synthetic thiazolidine-2,4-dione derivatives and their specific pharmacodynamic aspects

被引:2
|
作者
Vulichi, Srinivasa R. [1 ,2 ]
Kabra, Atul [3 ]
Kumar, Rupak [4 ]
Suman, Kapur [2 ]
Rao, Chunduri Venkata [5 ]
Cruz-Martins, Natalia [6 ,7 ,8 ]
机构
[1] SV Univ, Sri Venkateswara Univ Coll Pharmaceut Sci, Tirupati, Andhra Pradesh, India
[2] BITS, Dept Biol Sci, Hyderabad Campus, Pilani, Telangana, India
[3] Raffles Univ, Sch Pharm, Alwar, Rajasthan, India
[4] FDA Bhawan, CDSCO, New Delhi, India
[5] Sri Venkateswara Univ, Dept Chem, Tirupati, Andhra Pradesh, India
[6] Univ Porto, Fac Med, Alameda Prof Hernani Monteiro, P-4200319 Porto, Portugal
[7] Univ Porto, Inst Res & Innovat Heath i3S, Rua Alfredo Allen, P-4200135 Porto, Portugal
[8] Univ Porto, Fac Psychol & Educ Sci, Lab Neuropsychophysiol, Porto, Portugal
关键词
Anti-diabetic; Insulin resistance; PPAR-gamma; Thiazolidinedione; Side effects; MOLECULAR DOCKING; LOBEGLITAZONE; AEGELINE; DESIGN;
D O I
10.1016/j.lfs.2021.119182
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Glitazones are synthetic derivatives of thiazolidinedione, and are designated as oral anti-diabetic agents, primarily acting on peroxisome proliferator-activated receptor-gamma (PPAR-y) receptors and driving some crucial metabolic pathways linked to glucose and lipid metabolism at transcriptional level. Despite presenting adverse effects, including weight gain, fluid retention, prostate hyperplasia, hyperinsulinemia, and myocardial infarction, they are still preferred in clinical settings due to their utmost efficacy and selectivity. However, these complications kept glitazones restrained for long-term usage. The present review briefly highlights some important synthetic derivatives of thiazolidine2,4-dione and emphasizes the influence of various structural manipulations on their bio-efficacy.
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页数:11
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