Hepatocyte

Target ID: CHEMBL613690

Organism: Homo sapiens

Type: CELL-LINE

View on ChEMBL

Molecules

Name SMILES Bioactivity Structure
FUROSEMIDE NS(=O)(=O)c1cc(C(=O)O)c(NCc2ccco2)cc1Cl Ki: 100000.0 nM
VORINOSTAT O=C(CCCCCCC(=O)Nc1ccccc1)NO Inhibition: 100.0 %
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
THEOPHYLLINE Cn1c(=O)c2[nH]cnc2n(C)c1=O ED50: 18.5 mg.kg-1
ACETAMINOPHEN CC(=O)Nc1ccc(O)cc1 Vdss: 0.95 L.kg-1
CAFFEINE Cn1c(=O)c2c(ncn2C)n(C)c1=O Vdss: 0.61 L.kg-1
SILDENAFIL CCCc1nn(C)c2c(=O)[nH]c(-c3cc(S(=O)(=O)N4CCN(C)CC4)ccc3OCC)nc12 Pc: 87000000.0 cm s-1
LINIFANIB Cc1ccc(F)c(NC(=O)Nc2ccc(-c3cccc4[nH]nc(N)c34)cc2)c1 IC50: 4.0 nM
TOFACITINIB C[C@@H]1CCN(C(=O)CC#N)C[C@@H]1N(C)c1ncnc2[nH]ccc12 IC50: 13.0 nM

Top Fragments

SMILES Avg pKi Count Structure
[5*]N[5*] 6.72 114
[5*]N([5*])C 8.27 58
c1ccccc1 None 51
O=c1[nH]c(=O)c2[nH]cnc2[nH]1 None 44
[16*]c1ccccc1 None 39