Structure activity relationship (SAR) and anticancer activity of pyrrolidine derivatives: Recent developments and future prospects (A review)

被引:28
|
作者
Bhat, Aeyaz Ahmad [1 ]
Singh, Iqubal [2 ]
Tandon, Nitin [1 ]
Tandon, Runjhun [1 ]
机构
[1] Lovely Profess Univ, Sch Chem Engn & Phys Sci, Dept Chem, Phagwara 144411, India
[2] Lovely Profess Univ, Sch Pharmaceut Sci, Phagwara 144411, India
关键词
Anticancer; Pyrrolidine derivatives; Spirooxindole; Thiazole; Metal complexes; Structure activity relationship (SAR); NITROGEN-CONTAINING HETEROCYCLES; BIOLOGICAL EVALUATION; 1,3-DIPOLAR CYCLOADDITION; MOLECULAR DOCKING; CANCER-DIAGNOSIS; DESIGN; ANALOGS; SPIROOXINDOLES; PROLINE; INHIBITORS;
D O I
10.1016/j.ejmech.2022.114954
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pyrrolidine molecules are a significant class of synthetic and natural plant metabolites, which show the diversity of pharmacological activities. An extensive variety of synthetic pyrrolidine compounds with numerous deriva-tization like spirooxindole, thiazole, metal complexes, coumarin, etc have revealed significant anticancer ac-tivity. Pyrrolidine molecules are found not only as potential anticancer candidates but also retain the lowest side effects. Depending upon the diverse substitution patterns of the derivatives, these molecules have demonstrated an incredible ability to regulate the various targets to give excellent anti-proliferative activities. Taking these into consideration, efforts have been taken by the scientific fraternity to design and develop a potent anticancer scaffold with negligible side effects. In the present review, we cover the latest advancements in the synthesis of pyrrolidine molecules which have promising anticancer activity toward numerous cancer cell lines. Additionally, it also highlights the effectiveness of derivatives via elucidation of Structural-Activity-Relationship (SAR) which is discussed in detail.
引用
收藏
页数:36
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