Carbonic anhydrase IX

Target ID: CHEMBL3594

Organism: Homo sapiens

Type: SINGLE PROTEIN

View on ChEMBL

Molecules

Name SMILES Bioactivity Structure
DORZOLAMIDE CCN[C@H]1C[C@H](C)S(=O)(=O)c2sc(S(N)(=O)=O)cc21 Ki: 50000.0 nM
ACETAZOLAMIDE CC(=O)Nc1nnc(S(N)(=O)=O)s1 Ki: 250.0 nM
TOPIRAMATE CC1(C)O[C@@H]2[C@@H](CO[C@@]3(COS(N)(=O)=O)OC(C)(C)O[C@@H]23)O1 Ki: 250.0 nM
DICHLORPHENAMIDE NS(=O)(=O)c1cc(Cl)c(Cl)c(S(N)(=O)=O)c1 Ki: 1200.0 nM
MAFENIDE NCc1ccc(S(N)(=O)=O)cc1 Ki: 25000.0 nM
VALDECOXIB Cc1onc(-c2ccccc2)c1-c1ccc(S(N)(=O)=O)cc1 Ki: 54000.0 nM
SULFANILAMIDE Nc1ccc(S(N)(=O)=O)cc1 Ki: 28000.0 nM
ETHOXZOLAMIDE CCOc1ccc2nc(S(N)(=O)=O)sc2c1 Ki: 25.0 nM
BRINZOLAMIDE CCN[C@H]1CN(CCCOC)S(=O)(=O)c2sc(S(N)(=O)=O)cc21 Ki: 37.0 nM
INDISULAM NS(=O)(=O)c1ccc(S(=O)(=O)Nc2cccc3c(Cl)c[nH]c23)cc1 Ki: 30.0 nM
METHAZOLAMIDE CC(=O)/N=c1/sc(S(N)(=O)=O)nn1C Ki: 50.0 nM
ACETOHYDROXAMIC ACID CC(=O)NO IC50: 47000.0 nM

Top Fragments

SMILES Avg pKi Count Structure
c1ccccc1 5.03 104
[4*]CC 6.38 102
[16*]c1ccc(S(N)(=O)=O)cc1 4.44 69
[5*]N[5*] 7.04 67
O=S1(=O)CCCc2ccsc21 4.3 36