Current progress, challenges and future prospects of indazoles as protein kinase inhibitors for the treatment of cancer

被引:13
|
作者
Tandon, Nitin [1 ]
Luxami, Vijay [2 ]
Kant, Divya [1 ]
Tandon, Runjhun [1 ]
Paul, Kamaldeep [2 ]
机构
[1] Lovely Profess Univ, Sch Chem Engn & Phys Sci, Phagwara 144411, India
[2] Thapar Inst Engn & Technol, Sch Chem & Biochem, Patiala 147004, Punjab, India
关键词
GROWTH-FACTOR; BREAST-CANCER; BIOLOGICAL EVALUATION; CELL-PROLIFERATION; TYROSINE KINASE; AURORA-KINASE; CONSTITUTIVE ACTIVATION; EPIGENETIC INACTIVATION; ANTICANCER AGENTS; MOLECULAR-CLONING;
D O I
10.1039/d1ra03979b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The indazole core is an interesting pharmacophore due to its applications in medicinal chemistry. In the past few years, this moiety has been used for the synthesis of kinase inhibitors. Many researchers have demonstrated the use of indazole derivatives as specific kinase inhibitors, including tyrosine kinase and serine/threonine kinases. A number of anticancer drugs with an indazole core are commercially available, e.g. axitinib, linifanib, niraparib, and pazopanib. Indazole derivatives are applied for the targeted treatment of lung, breast, colon, and prostate cancers. In this review, we compile the current development of indazole derivatives as kinase inhibitors and their application as anticancer agents in the past five years.
引用
收藏
页码:25228 / 25257
页数:30
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