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ChEMBL ligand: CHEMBL524266 |
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DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
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ALK receptor tyrosine kinase/ALK tyrosine kinase receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4247] [GtoPdb: 1839] [UniProtKB: Q9UM73] | ||||||||
ChEMBL | Inhibition of ALK | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
protein kinase, cAMP-dependent, catalytic, alpha subunit/cAMP-dependent protein kinase alpha-catalytic subunit in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4101] [GtoPdb: 1476] [UniProtKB: P17612] | ||||||||
ChEMBL | Inhibition of PKAalpha | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
cell division cycle 7/Cell division cycle 7-related protein kinase in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5443] [GtoPdb: 1960] [UniProtKB: O00311] | ||||||||
GtoPdb | - | - | 9.3 | pKi | 0.5 | nM | Ki | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
ChEMBL | Inhibition of human Cdc7 assessed as inhibition of rate of phosphorylation of Mcm2 protein | B | 8.7 | pIC50 | 2 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
GtoPdb | - | - | 8.7 | pIC50 | 2 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
cyclin dependent kinase 2/Cyclin-dependent kinase 2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL301] [GtoPdb: 1973] [UniProtKB: P24941] | ||||||||
GtoPdb | CDK2/cyclin A complex | - | 6.86 | pIC50 | 138 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
ChEMBL | Inhibition of Cdk2A | B | 6.86 | pIC50 | 138 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
cyclin dependent kinase 4/Cyclin-dependent kinase 4 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL331] [GtoPdb: 1976] [UniProtKB: P11802] | ||||||||
ChEMBL | Inhibition of CDK4 | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
cyclin dependent kinase 5/Cyclin-dependent kinase 5/CDK5 activator 1 in Human (target type: PROTEIN COMPLEX) [ChEMBL: CHEMBL1907600] [GtoPdb: 1977] [UniProtKB: Q00535, Q15078] | ||||||||
ChEMBL | Inhibition of CDK5/p25 | B | 5.79 | pIC50 | 1620 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
cyclin dependent kinase 9/Cyclin-dependent kinase 9 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3116] [GtoPdb: 1981] [UniProtKB: P50750] | ||||||||
GtoPdb | CDK9/cyclin T complex | - | 7.55 | pIC50 | 28 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
ChEMBL | Inhibition of CDK9 | B | 7.55 | pIC50 | 28 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
fibroblast growth factor receptor 1/Fibroblast growth factor receptor 1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3650] [GtoPdb: 1808] [UniProtKB: P11362] | ||||||||
ChEMBL | Inhibition of FGFR1 | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
glycogen synthase kinase 3 beta/Glycogen synthase kinase-3 beta in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL262] [GtoPdb: 2030] [UniProtKB: P49841] | ||||||||
ChEMBL | Inhibition of GSK3-beta | B | 6.84 | pIC50 | 146 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
GtoPdb | - | - | 6.84 | pIC50 | 146 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
MET proto-oncogene, receptor tyrosine kinase/Hepatocyte growth factor receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3717] [GtoPdb: 1815] [UniProtKB: P08581] | ||||||||
ChEMBL | Inhibition of MET | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
High affinity immunoglobulin gamma Fc receptor I in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5349] [UniProtKB: P12314] | ||||||||
ChEMBL | Inhibition of IGFR1 | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
inhibitor of nuclear factor kappa B kinase subunit epsilon/Inhibitor of nuclear factor kappa B kinase epsilon subunit in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3529] [GtoPdb: 2040] [UniProtKB: Q14164] | ||||||||
ChEMBL | Inhibition of IKKi | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
Insulin receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1981] [GtoPdb: 1800] [UniProtKB: P06213] | ||||||||
ChEMBL | Inhibition of IR | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
MAPK activated protein kinase 2/MAP kinase-activated protein kinase 2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2208] [GtoPdb: 2094] [UniProtKB: P49137] | ||||||||
ChEMBL | Inhibition of MK2 | B | 6.29 | pIC50 | 510 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
mitogen-activated protein kinase 1/MAP kinase ERK2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4040] [GtoPdb: 1495] [UniProtKB: P28482] | ||||||||
ChEMBL | Inhibition of ERK2 | B | 6.07 | pIC50 | 846 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
mitogen-activated protein kinase 11/MAP kinase p38 beta in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3961] [GtoPdb: 1500] [UniProtKB: Q15759] | ||||||||
ChEMBL | Inhibition of P38beta | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
neurotrophic receptor tyrosine kinase 1/Nerve growth factor receptor Trk-A in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2815] [GtoPdb: 1817] [UniProtKB: P04629] | ||||||||
ChEMBL | Inhibition of TRKA | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
protein kinase C beta/Protein kinase C beta in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3045] [GtoPdb: 1483] [UniProtKB: P05771] | ||||||||
ChEMBL | Inhibition of PKCbeta | B | 5.94 | pIC50 | 1149 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
pyruvate dehydrogenase kinase 1/Pyruvate dehydrogenase kinase isoform 1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4766] [GtoPdb: 2915] [UniProtKB: Q15118] | ||||||||
ChEMBL | Inhibition of PDK1 | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
STE20 like kinase/Serine/threonine-protein kinase 2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4202] [GtoPdb: 2200] [UniProtKB: Q9H2G2] | ||||||||
ChEMBL | Inhibition of STLK2 | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
AKT serine/threonine kinase 1/Serine/threonine-protein kinase AKT in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4282] [GtoPdb: 1479] [UniProtKB: P31749] | ||||||||
ChEMBL | Inhibition of AKT1 | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
aurora kinase A/Serine/threonine-protein kinase Aurora-A in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4722] [GtoPdb: 1936] [UniProtKB: O14965] | ||||||||
ChEMBL | Inhibition of AUR2 | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
ChEMBL | Inhibition of AUR1 | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
checkpoint kinase 1/Serine/threonine-protein kinase Chk1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4630] [GtoPdb: 1987] [UniProtKB: O14757] | ||||||||
ChEMBL | Inhibition of CHK1 | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
serine/threonine-protein kinase MST4/Serine/threonine-protein kinase MST4 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5941] [GtoPdb: 2287] [UniProtKB: Q9P289] | ||||||||
ChEMBL | Inhibition of MST4 | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
NIMA related kinase 6/Serine/threonine-protein kinase NEK6 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4309] [GtoPdb: 2121] [UniProtKB: Q9HC98] | ||||||||
ChEMBL | Inhibition of NEK6 | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
serine/threonine-protein kinase NIM1/Serine/threonine-protein kinase NIM1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3542] [GtoPdb: 2291] [UniProtKB: Q8IY84] | ||||||||
ChEMBL | Inhibition of NIM1 | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
GtoPdb | - | - | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
p21 (RAC1) activated kinase 4/Serine/threonine-protein kinase PAK 4 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4482] [GtoPdb: 2136] [UniProtKB: O96013] | ||||||||
ChEMBL | Inhibition of PAK4 | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
polo like kinase 1/Serine/threonine-protein kinase PLK1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3024] [GtoPdb: 2168] [UniProtKB: P53350] | ||||||||
ChEMBL | Inhibition of PLK1 | B | 6.24 | pIC50 | 574 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
TAO kinase 3/Serine/threonine-protein kinase TAO3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5701] [GtoPdb: 2235] [UniProtKB: Q9H2K8] | ||||||||
ChEMBL | Inhibition of TAO3 | B | 6.9 | pIC50 | 126 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
GtoPdb | - | - | 6.9 | pIC50 | 126 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
KIT proto-oncogene, receptor tyrosine kinase/Stem cell growth factor receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1936] [GtoPdb: 1805] [UniProtKB: P10721] | ||||||||
ChEMBL | Inhibition of KIT | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
ABL proto-oncogene 1, non-receptor tyrosine kinase/Tyrosine-protein kinase ABL in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1862] [GtoPdb: 1923] [UniProtKB: P00519] | ||||||||
ChEMBL | Inhibition of ABL | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
LCK proto-oncogene, Src family tyrosine kinase/Tyrosine-protein kinase LCK in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL258] [GtoPdb: 2053] [UniProtKB: P06239] | ||||||||
ChEMBL | Inhibition of LCK | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
ret proto-oncogene/Tyrosine-protein kinase receptor RET in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2041] [GtoPdb: 2185] [UniProtKB: P07949] | ||||||||
ChEMBL | Inhibition of RET | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
fms related receptor tyrosine kinase 4/Vascular endothelial growth factor receptor 3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1955] [GtoPdb: 1814] [UniProtKB: P35916] | ||||||||
ChEMBL | Inhibition of VEGFR3 | B | 5.4 | pIC50 | >4000 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
cyclin dependent kinase 1 in Human [GtoPdb: 1961] [UniProtKB: P06493] | ||||||||
GtoPdb | CDK1/cyclin B complex | - | 7.52 | pIC50 | 30 | nM | IC50 | J Med Chem (2009) 52: 293-307 [PMID:19115845] |
ChEMBL data shown on this page come from version 34:
Zdrazil B, Felix E, Hunter F, Manners EJ, Blackshaw J, Corbett S, de Veij M, Ioannidis H, Lopez DM, Mosquera JF, Magarinos MP, Bosc N, Arcila R, Kizilören T, Gaulton A, Bento AP, Adasme MF, Monecke P, Landrum GA, Leach AR. (2024). The ChEMBL Database in 2023: a drug discovery platform spanning multiple bioactivity data types and time periods. Nucleic Acids Res., 52(D1). DOI: 10.1093/nar/gkad1004. [EPMCID:10767899] [PMID:37933841]
Davies M, Nowotka M, Papadatos G, Dedman N, Gaulton A, Atkinson F, Bellis L, Overington JP. (2015) 'ChEMBL web services: streamlining access to drug discovery data and utilities.' Nucleic Acids Res., 43(W1). DOI: 10.1093/nar/gkv352. [EPMCID:25883136]