null

SMILES NS(=O)(=O)c1ccc(NC(=O)CSC(=S)N2CCN(CC2)c2ncccn2)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 = 50552008   

TargetCarbonic anhydrase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50552008(CHEMBL4750069)copy SMILES
Affinity DataKi:  41nMAssay 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 2(Homo sapiens (Human))TBA
LigandPNGBDBM50552008(CHEMBL4750069)copy SMILES
Affinity DataKi:  107nMAssay 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
LigandPNGBDBM50552008(CHEMBL4750069)copy SMILES
Affinity DataIC50: 65nMAssay 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
LigandPNGBDBM50552008(CHEMBL4750069)copy SMILES
Affinity DataIC50: 191nMAssay 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