Cytochrome P450 2C8

Target ID: CHEMBL3721

Organism: Homo sapiens

Type: SINGLE PROTEIN

View on ChEMBL

Molecules

Name SMILES Bioactivity Structure
IMATINIB MESYLATE CS(=O)(=O)O.Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)cc2)cc1Nc1nccc(-c2cccnc2)n1 EC50: 90.0 nM
FUROSEMIDE NS(=O)(=O)c1cc(C(=O)O)c(NCc2ccco2)cc1Cl Ki: 100000.0 nM
MIFEPRISTONE CC#C[C@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CCC4=C3[C@@H](c3ccc(N(C)C)cc3)C[C@@]21C IC50: 0.028 nM
ROSUVASTATIN CC(C)c1nc(N(C)S(C)(=O)=O)nc(-c2ccc(F)cc2)c1/C=C/[C@@H](O)C[C@@H](O)CC(=O)O Ki: 0.9 nM
ACETAMINOPHEN CC(=O)Nc1ccc(O)cc1 Vdss: 0.95 L.kg-1
ASTEMIZOLE COc1ccc(CCN2CCC(Nc3nc4ccccc4n3Cc3ccc(F)cc3)CC2)cc1 Binding energy: 11.3 kCal mol-1
CAFFEINE Cn1c(=O)c2c(ncn2C)n(C)c1=O Vdss: 0.61 L.kg-1
QUERCETIN O=c1c(O)c(-c2ccc(O)c(O)c2)oc2cc(O)cc(O)c12 IC50: 32870.0 nM
TRIMETHOPRIM COc1cc(Cc2cnc(N)nc2N)cc(OC)c1OC IC50: 12000.0 nM
TAMOXIFEN CC/C(=C(\c1ccccc1)c1ccc(OCCN(C)C)cc1)c1ccccc1 IC50: 6750.0 nM

Top Fragments

SMILES Avg pKi Count Structure
[16*]c1ccc([16*])cc1 7.62 104
[5*]N[5*] 5.89 81
[4*]C[8*] 5.89 63
[5*]N(C)C 8.0 59
[8*]C[8*] 4.92 45