THLE-2

Target ID: CHEMBL4296500

Organism: Homo sapiens

Type: CELL-LINE

View on ChEMBL

Molecules

Name SMILES Bioactivity Structure
GENISTEIN O=c1c(-c2ccc(O)cc2)coc2cc(O)cc(O)c12 IC50: 1000.0 nM
VARDENAFIL CCCc1nc(C)c2c(=O)nc(-c3cc(S(=O)(=O)N4CCN(CC)CC4)ccc3OCC)[nH]n12 IC50: 0.7 nM
VORINOSTAT O=C(CCCCCCC(=O)Nc1ccccc1)NO Inhibition: 100.0 %
SILDENAFIL CCCc1nn(C)c2c(=O)[nH]c(-c3cc(S(=O)(=O)N4CCN(C)CC4)ccc3OCC)nc12 Pc: 87000000.0 cm s-1
FLUCONAZOLE OC(Cn1cncn1)(Cn1cncn1)c1ccc(F)cc1F IC80: 2.8 ug ml-1
TADALAFIL CN1CC(=O)N2[C@H](c3ccc4c(c3)OCO4)c3[nH]c4ccccc4c3C[C@@H]2C1=O IC50: 6.7 nM
ALVOCIDIB CN1CC[C@H](c2c(O)cc(O)c3c(=O)cc(-c4ccccc4Cl)oc23)[C@H](O)C1 IC50: 330.0 nM
BAICALEIN O=c1cc(-c2ccccc2)oc2cc(O)c(O)c(O)c12 Inhibition: 57.0 %

Top Fragments

SMILES Avg pKi Count Structure
[4*]CC 9.15 78
[12*]S(=O)(=O)c1ccc([16*])c([16*])c1 9.15 78
[3*]O[3*] 9.15 78
[8*]CCC 9.15 78
[16*]c1ccccc1 None 78