Table 1 Classification of CK2 inhibitors

From: Protein kinase CK2: a potential therapeutic target for diverse human diseases

Class of the inhibitor

Subclass

Representative compounds

References

ATP-competitive inhibitors

Polyhalogenated benzimidazoles and benzotriazoles

TBB

307

 

TDB

308

 

DMAT

309

Flavonoids

Quercetin

310

Coumarins

Ellagic acid

311

Anthraquinones

Quinalizarin

312

Pyrazolotriazines

Compound 9e

28

SRPIN803 derivatives

Compound 4

313

Carboxyl acid derivatives

TBCA

314

IQA

310

CX-4945

315

CX-5011

27

Triazol bromoguaiacol derivatives

GO289

29

Peptide-competitive inhibitors

 

CIGB-300

26

Allosteric inhibitors

α/β interface targeting

Pc

24

 

POMs

25

Bi-substrate inhibitors

 

ARCs

22

K137-E4

23

Multi-target inhibitors

CK2 and HDAC targeting

 

316

CX-4945 + CisPt

 

317

  1. Compounds in human clinical trials are in bold
  2. TBB 4,5,6,7-tetrabromo-2-azabenzimidazole, TDB 1-(β-D-2′-deoxyribofuranosyl)-4,5,6,7-tetrabromo-1H-benzimidazole, DMAT 2-dimethylamino-4,5,6,7-tetrabromo-1H-benzimidazole, TBCA tetrabromo-cinnamic acid, IQA [5-oxo-5,6-dihydro-indolo(1,2-a)quinazolin-7-yl]acetic acid, POMs polyoxometalates, HDAC histone deacetylase, CisPt cisplatin