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World J Pharmacol. Dec 9, 2014; 3(4): 162-173
Published online Dec 9, 2014. doi: 10.5497/wjp.v3.i4.162
Published online Dec 9, 2014. doi: 10.5497/wjp.v3.i4.162
Tyrosine protein kinases | |
Epidermal growth factor receptor (EGFR; Erb-1; HER1 in humans) | Receptor |
Human epidermal growth factor receptor 2 (HER2; erbB2; protooncogene Neu) | Receptor |
Vascular endothelial growth factor receptor 2 | Receptor |
Janus kinase 2 | Non-receptor |
Janus kinase 3 | Non-receptor |
Spleen tyrosine kinase | Non-receptor |
Zeta-chain-associated protein kinase 70 | Non-receptor |
TEK tyrosine kinase, endothelial | Receptor |
Serine/threonine protein kinases | |
Dual-specificity tyrosine-phosphorylation regulated kinase 1A | Non-receptor |
Cdc2-like kinase | Non-receptor |
Checkpoint kinase 1 | Non-receptor |
Human inhibitor nuclear-factor κB kinase 2 | Non-receptor |
Cyclin-dependent kinase 1 | Non-receptor |
Cyclin-dependent kinase 2 | Non-receptor |
Polo-like kinase | Non-receptor |
c-Jun N-terminal kinase 3 | Non-receptor |
Glycogen synthase kinase 3 | Non-receptor |
Mammalian target of rapamycin | Non-receptor |
p38 mitogen-activated protein kinase | Non-receptor |
Protein kinase B | Non-receptor |
- Citation: Starosyla SA, Volynets GP, Bdzhola VG, Golub AG, Yarmoluk SM. Pharmacophore approaches in protein kinase inhibitors design. World J Pharmacol 2014; 3(4): 162-173
- URL: https://www.wjgnet.com/2220-3192/full/v3/i4/162.htm
- DOI: https://dx.doi.org/10.5497/wjp.v3.i4.162