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ChEMBL ligand: CHEMBL1270230 |
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DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
---|---|---|---|---|---|---|---|---|
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
cyclin dependent kinase 9/CDK9/cyclin T1 in Human (target type: PROTEIN COMPLEX) [ChEMBL: CHEMBL2111389] [GtoPdb: 1981] [UniProtKB: O60563, P50750] | ||||||||
GtoPdb | - | - | 6.4 | pIC50 | 394 | nM | IC50 | J Med Chem (2010) 53: 7296-315 [PMID:20873740] |
ChEMBL | Inhibition of Cdk9/cyclin T | B | 6.4 | pIC50 | 394 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
cell division cycle 7/Cell division cycle 7-related protein kinase in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5443] [GtoPdb: 1960] [UniProtKB: O00311] | ||||||||
ChEMBL | Inhibition of Cdc7 | B | 7.66 | pIC50 | 22 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
GtoPdb | - | - | 7.66 | pIC50 | 22 | nM | IC50 | J Med Chem (2010) 53: 7296-315 [PMID:20873740] |
cyclin dependent kinase 1/Cyclin-dependent kinase 1/cyclin B in Human (target type: PROTEIN COMPLEX) [ChEMBL: CHEMBL2094127] [GtoPdb: 1961] [UniProtKB: O95067, P06493, P14635, Q8WWL7] | ||||||||
ChEMBL | Inhibition of Cdk1/cyclin B | B | 5.51 | pIC50 | 3100 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
cyclin dependent kinase 2/Cyclin-dependent kinase 2/cyclin A in Human (target type: PROTEIN COMPLEX) [ChEMBL: CHEMBL2094128] [GtoPdb: 1973] [UniProtKB: P20248, P24941, P78396] | ||||||||
ChEMBL | Inhibition of Cdk2/cyclin A | B | 5.55 | pIC50 | 2800 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
cyclin dependent kinase 2/Cyclin-dependent kinase 2/cyclin E in Human (target type: PROTEIN COMPLEX) [ChEMBL: CHEMBL2094126] [GtoPdb: 1973] [UniProtKB: O96020, P24864, P24941] | ||||||||
ChEMBL | Inhibition of Cdk2/cyclin E | B | 5.57 | pIC50 | 2700 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
cyclin dependent kinase 4/Cyclin-dependent kinase 4/cyclin D1 in Human (target type: PROTEIN COMPLEX) [ChEMBL: CHEMBL1907601] [GtoPdb: 1976] [UniProtKB: P11802, P24385] | ||||||||
ChEMBL | Inhibition of Cdk4/cyclin D1 | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
TTK protein kinase/Dual specificity protein kinase TTK in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3983] [GtoPdb: 2264] [UniProtKB: P33981] | ||||||||
ChEMBL | Inhibition of MPS1 | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
eukaryotic translation initiation factor 2 alpha kinase 3/Eukaryotic translation initiation factor 2-alpha kinase 3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL6030] [GtoPdb: 2017] [UniProtKB: Q9NZJ5] | ||||||||
ChEMBL | Inhibition of PERK | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
protein tyrosine kinase 2/Focal adhesion kinase 1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2695] [GtoPdb: 2180] [UniProtKB: Q05397] | ||||||||
ChEMBL | Inhibition of FAK | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | 5.86 | pIC50 | 1390 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
inhibitor of nuclear factor kappa B kinase subunit beta/Inhibitor of nuclear factor kappa B kinase beta subunit in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1991] [GtoPdb: 2039] [UniProtKB: O14920] | ||||||||
ChEMBL | Inhibition of IKK2 | B | 5.42 | pIC50 | 3800 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
Insulin-like growth factor I receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1957] [GtoPdb: 1801] [UniProtKB: P08069] | ||||||||
ChEMBL | Inhibition of IGFR1 | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
Insulin receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1981] [GtoPdb: 1800] [UniProtKB: P06213] | ||||||||
ChEMBL | Inhibition of IR | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
mitogen-activated protein kinase 14/MAP kinase p38 alpha in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL260] [GtoPdb: 1499] [UniProtKB: Q16539] | ||||||||
ChEMBL | Inhibition of P38alpha | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | 5.43 | pIC50 | 3700 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
aurora kinase A/Serine/threonine-protein kinase Aurora-A in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4722] [GtoPdb: 1936] [UniProtKB: O14965] | ||||||||
ChEMBL | Inhibition of AUR1 | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
aurora kinase B/Serine/threonine-protein kinase Aurora-B in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2185] [GtoPdb: 1937] [UniProtKB: Q96GD4] | ||||||||
ChEMBL | Inhibition of AUR2 | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
eukaryotic elongation factor 2 kinase/Serine/threonine-protein kinase EEF2K in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5026] [GtoPdb: 2014] [UniProtKB: O00418] | ||||||||
ChEMBL | Inhibition of EEF2K | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
Pim-1 proto-oncogene, serine/threonine kinase/Serine/threonine-protein kinase PIM1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2147] [GtoPdb: 2158] [UniProtKB: P11309] | ||||||||
ChEMBL | Inhibition of PIM1 | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
TAO kinase 1/Serine/threonine-protein kinase TAO1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5261] [GtoPdb: 2233] [UniProtKB: Q7L7X3] | ||||||||
ChEMBL | Inhibition of TAO1 | B | 6.38 | pIC50 | 420 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
GtoPdb | - | - | 6.38 | pIC50 | 420 | nM | IC50 | J Med Chem (2010) 53: 7296-315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
protein tyrosine kinase 6/Tyrosine-protein kinase BRK in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4601] [GtoPdb: 2182] [UniProtKB: Q13882] | ||||||||
ChEMBL | Inhibition of BRK | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
Janus kinase 2/Tyrosine-protein kinase JAK2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2971] [GtoPdb: 2048] [UniProtKB: O60674] | ||||||||
ChEMBL | Inhibition of JAK2 | B | 5.48 | pIC50 | 3300 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
ChEMBL | Inhibition of recombinant human JAK2 (808-1132 residues) using LPLDKDYYVVREPGQ as substrate by radiometric assay in presence of [33P]-gamma-ATP | B | 5.49 | pIC50 | 3200 | nM | IC50 | Bioorg Med Chem (2014) 22: 4998-5012 [PMID:25009002] |
Janus kinase 3/Tyrosine-protein kinase JAK3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2148] [GtoPdb: 2049] [UniProtKB: P52333] | ||||||||
ChEMBL | Inhibition of JAK3 | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
fms related receptor tyrosine kinase 3/Tyrosine-protein kinase receptor FLT3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1974] [GtoPdb: 1807] [UniProtKB: P36888] | ||||||||
ChEMBL | Inhibition of FLT3 | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
spleen associated tyrosine kinase/Tyrosine-protein kinase SYK in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2599] [GtoPdb: 2230] [UniProtKB: P43405] | ||||||||
ChEMBL | Inhibition of SYK | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
zeta chain of T cell receptor associated protein kinase 70/Tyrosine-protein kinase ZAP-70 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2803] [GtoPdb: 2285] [UniProtKB: P43403] | ||||||||
ChEMBL | Inhibition of ZAP70 | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
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 | pIC50 | >10000 | nM | IC50 | J Med Chem (2010) 53: 7296-7315 [PMID:20873740] |
ChEMBL data shown on this page come from version 33:
Mendez D, Gaulton A, Bento AP, Chambers J, De Veij M, Félix E, Magariños MP, Mosquera JF, Mutowo P, Nowotka M, Gordillo-Marañón M, Hunter F, Junco L, Mugumbate G, Rodriguez-Lopez M, Atkinson F, Bosc N, Radoux CJ, Segura-Cabrera A, Hersey A, Leach AR. (2019) 'ChEMBL: towards direct deposition of bioassay data' Nucleic Acids Res., 47(D1). DOI: 10.1093/nar/gky1075. [EPMCID:30398643]
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]