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ChEMBL ligand: CHEMBL583042 |
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DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
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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 | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a PRKACA | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
citron rho-interacting serine/threonine kinase/Citron Rho-interacting kinase in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5579] [GtoPdb: 1509] [UniProtKB: O14578] | ||||||||
ChEMBL | Inhibition of CIT | B | 5 | pKi | >10000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a CIT | B | 5 | pKi | >10000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
mitogen-activated protein kinase 10/c-Jun N-terminal kinase 3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2637] [GtoPdb: 1498] [UniProtKB: P53779] | ||||||||
ChEMBL | Inhibition of JNK3 | B | 5.85 | pKi | 1400 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a MAPK10 | B | 5.85 | pKi | 1400 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
cyclin dependent kinase 2/Cyclin-dependent kinase 2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL301] [GtoPdb: 1973] [UniProtKB: P24941] | ||||||||
ChEMBL | Inhibition of CDK2 | B | 6.07 | pKi | 852 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
GtoPdb | - | - | 6.07 | pKi | 852 | nM | Ki | J Med Chem (2009) 52: 6362-8 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a CDK2 | B | 6.07 | pKi | 850 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
mitogen-activated protein kinase kinase 1/Dual specificity mitogen-activated protein kinase kinase 1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3587] [GtoPdb: 2062] [UniProtKB: Q02750] | ||||||||
ChEMBL | Inhibition of MEK1 | B | 5.4 | pKi | >4000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a MAP2K1 | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
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 | pKi | >10000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a PTK2 | B | 5 | pKi | >10000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
glycogen synthase kinase 3 alpha/Glycogen synthase kinase-3 alpha in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2850] [GtoPdb: 2029] [UniProtKB: P49840] | ||||||||
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a GSK3A | B | 6.4 | pKi | 400 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
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 | pKi | >4000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a MET | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
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 | 5.3 | pKi | >5000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a IKBKE | B | 5.3 | pKi | >5000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
interleukin 1 receptor associated kinase 1/Interleukin-1 receptor-associated kinase 1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3357] [GtoPdb: 2042] [UniProtKB: P51617] | ||||||||
ChEMBL | Inhibition of IRAK1 | B | 5 | pKi | >10000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a IRAK1 | B | 5 | pKi | >10000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
interleukin 1 receptor associated kinase 4/Interleukin-1 receptor-associated kinase 4 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3778] [GtoPdb: 2045] [UniProtKB: Q9NWZ3] | ||||||||
ChEMBL | Inhibition of IRAK4 | B | 5.4 | pKi | >4000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a IRAK4 | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
mitogen-activated protein kinase 3/MAP kinase ERK1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3385] [GtoPdb: 1494] [UniProtKB: P27361] | ||||||||
ChEMBL | Affinity Biochemical interaction: (Enzymatic assay) EUB0000604a MAPK3 | B | 8.7 | pKi | <2 | nM | Ki | Affinity Biochemical Literature for EUbOPEN Chemogenomic Library |
mitogen-activated protein kinase 1/MAP kinase ERK2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4040] [GtoPdb: 1495] [UniProtKB: P28482] | ||||||||
ChEMBL | Inhibition of ERK2 after 10 mins by spectrophotometric coupled-enzyme assay | B | 8.7 | pKi | <2 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Affinity Biochemical interaction: (Enzymatic assay) EUB0000604a MAPK1 | B | 8.7 | pKi | <2 | nM | Ki | Affinity Biochemical Literature for EUbOPEN Chemogenomic Library |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a MAPK1 | B | 8.7 | pKi | <2 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
GtoPdb | - | - | 8.7 | pKi | <2 | nM | Ki | J Med Chem (2009) 52: 6362-8 [PMID:19827834] |
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 | 5.4 | pKi | >4000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a MAPK14 | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
mitogen-activated protein kinase kinase kinase 10/Mitogen-activated protein kinase kinase kinase 10 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2873] [GtoPdb: 2070] [UniProtKB: Q02779] | ||||||||
ChEMBL | Inhibition of MLK2 | B | 5 | pKi | >10000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a MAP3K10 | B | 5 | pKi | >10000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
mitogen-activated protein kinase kinase kinase 14/Mitogen-activated protein kinase kinase kinase 14 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5888] [GtoPdb: 2074] [UniProtKB: Q99558] | ||||||||
ChEMBL | Inhibition of NIK | B | 5.3 | pKi | >5000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a MAP3K14 | B | 5.3 | pKi | >5000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
mitogen-activated protein kinase kinase kinase 3/Mitogen-activated protein kinase kinase kinase 3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5970] [GtoPdb: 2078] [UniProtKB: Q99759] | ||||||||
ChEMBL | Inhibition of MEKK3 | B | 5.4 | pKi | >4000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a MAP3K3 | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
mitogen-activated protein kinase kinase kinase 7/Mitogen-activated protein kinase kinase kinase 7 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5776] [GtoPdb: 2082] [UniProtKB: O43318] | ||||||||
ChEMBL | Inhibition of TAK1 | B | 5.52 | pKi | 3000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a MAP3K7 | B | 5.52 | pKi | 3000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
mitogen-activated protein kinase kinase kinase 8/Mitogen-activated protein kinase kinase kinase 8 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4899] [GtoPdb: 2083] [UniProtKB: P41279] | ||||||||
ChEMBL | Inhibition of COT | B | 5.4 | pKi | >4000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a MAP3K8 | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
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 | pKi | >10000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a PDK1 | B | 5 | pKi | >10000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
Rho associated coiled-coil containing protein kinase 1/Rho-associated protein kinase 1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3231] [GtoPdb: 1503] [UniProtKB: Q13464] | ||||||||
ChEMBL | Inhibition of ROCK1 | B | 5.85 | pKi | 1400 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a ROCK1 | B | 5.85 | pKi | 1400 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
AKT serine/threonine kinase 3/Serine/threonine-protein kinase AKT3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4816] [GtoPdb: 2286] [UniProtKB: Q9Y243] | ||||||||
ChEMBL | Inhibition of AKT3 | B | 5.4 | pKi | >4000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a AKT3 | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
aurora kinase A/Serine/threonine-protein kinase Aurora-A in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4722] [GtoPdb: 1936] [UniProtKB: O14965] | ||||||||
ChEMBL | Inhibition of AURA | B | 6.27 | pKi | 540 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a STK6 | B | 6.27 | pKi | 540 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
GtoPdb | - | - | 6.27 | pKi | 540 | nM | Ki | J Med Chem (2009) 52: 6362-8 [PMID:19827834] |
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 | 5.4 | pKi | >4000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a PLK1 | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
serum/glucocorticoid regulated kinase 1/Serine/threonine-protein kinase Sgk1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2343] [GtoPdb: 1534] [UniProtKB: O00141] | ||||||||
ChEMBL | Inhibition of SGK1 | B | 5 | pKi | >10000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a SGK1 | B | 5 | pKi | >10000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
TANK binding kinase 1/Serine/threonine-protein kinase TBK1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5408] [GtoPdb: 2237] [UniProtKB: Q9UHD2] | ||||||||
ChEMBL | Inhibition of NAK | B | 5 | pKi | >10000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a TBK1 | B | 5 | pKi | >10000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
IL2 inducible T cell kinase/Tyrosine-protein kinase ITK/TSK in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2959] [GtoPdb: 2046] [UniProtKB: Q08881] | ||||||||
ChEMBL | Inhibition of ITK | B | 5.4 | pKi | >4000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a ITK | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
Janus kinase 2/Tyrosine-protein kinase JAK2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2971] [GtoPdb: 2048] [UniProtKB: O60674] | ||||||||
ChEMBL | Inhibition of JAK2 | B | 5.4 | pKi | >4000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a JAK2 | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
Janus kinase 3/Tyrosine-protein kinase JAK3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2148] [GtoPdb: 2049] [UniProtKB: P52333] | ||||||||
ChEMBL | Inhibition of JAK3 | B | 5.4 | pKi | >4000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a JAK3 | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
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 | 5.85 | pKi | 1400 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a FLT3 | B | 5.85 | pKi | 1400 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
SRC proto-oncogene, non-receptor tyrosine kinase/Tyrosine-protein kinase SRC in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL267] [GtoPdb: 2206] [UniProtKB: P12931] | ||||||||
ChEMBL | Inhibition of SRC | B | 5.4 | pKi | >4000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a SRC | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
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 | 5.4 | pKi | >4000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a SYK | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
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 | 5.4 | pKi | >4000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a ZAP70 | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
kinase insert domain receptor/Vascular endothelial growth factor receptor 2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL279] [GtoPdb: 1813] [UniProtKB: P35968] | ||||||||
ChEMBL | Inhibition of KDR | B | 5.4 | pKi | >4000 | nM | Ki | J Med Chem (2009) 52: 6362-6368 [PMID:19827834] |
ChEMBL | Selectivity interaction (Kinase counterscreening (biochemical assay)) EUB0000604a KDR | B | 5.4 | pKi | >4000 | nM | Ki | Selectivity Literature for EUbOPEN Chemogenomic Library |
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]