Recent Advances in the Discovery of CK2 Inhibitors

被引:4
|
作者
Al-Qadhi, Mustafa A. [1 ]
Yahya, Tawfeek A. A. [2 ]
El-Nassan, Hala B. [3 ]
机构
[1] Sanaa Univ, Fac Pharm, Dept Med Chem, Sanaa, Yemen
[2] Sanaa Univ, Fac Pharm, Dept Med Chem, Sanaa, Yemen
[3] Cairo Univ, Fac Pharm, Pharmaceut Organ Chem Dept, Cairo 11562, Egypt
来源
ACS OMEGA | 2024年 / 9卷 / 19期
关键词
PROTEIN-KINASE CK2; CANCER-CELL STEMNESS; CATALYTIC SUBUNIT; ATP SITE; PEPTIDE; CX-4945; BINDING; DESIGN; TARGET; ANGIOGENESIS;
D O I
10.1021/acsomega.3c10478
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CK2 is a vital enzyme that phosphorylates a large number of substrates and thereby controls many processes in the body. Its upregulation was reported in many cancer types. Inhibitors of CK2 might have anticancer activity, and two compounds are currently under clinical trials. However, both compounds are ATP-competitive inhibitors that may have off-target side effects. The development of allosteric and dual inhibitors can overcome this drawback. These inhibitors showed higher selectivity and specificity for the CK2 enzyme compared to the ATP-competitive inhibitors. The present review summarizes the efforts exerted in the last five years in the design of CK2 inhibitors.
引用
收藏
页码:20702 / 20719
页数:18
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