null

SMILES Cc1ccc(CN2CCN(CC2)C(=S)SCC(=O)Nc2ccc(cc2)S(N)(=O)=O)cc1

InChI Key

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50552014   

TargetCarbonic anhydrase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50552014(CHEMBL4763412)copy SMILES
Affinity DataKi:  87nMAssay Description:Inhibition of human erythrocyte CA2 using 4-nitrophenyl acetate as substrate by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C2512XPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50552014(CHEMBL4763412)copy SMILES
Affinity DataKi:  280nMAssay Description:Inhibition of human erythrocyte CA1 b using 4-nitrophenyl acetate as substrate by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C2512XPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50552014(CHEMBL4763412)copy SMILES
Affinity DataIC50: 375nMAssay Description:Inhibition of human erythrocyte CA1 using 4-nitrophenyl acetate as substrate by spectrophotometryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C2512XPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50552014(CHEMBL4763412)copy SMILES
Affinity DataIC50: 131nMAssay Description:Inhibition of human erythrocyte CA2 using 4-nitrophenyl acetate as substrate by spectrophotometryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C2512XPubMed