null

SMILES NS(=O)(=O)c1ccc(cc1)-n1nc(cc1-c1cccs1)C(=O)N\N=C/c1ccc(cc1)[N+]([O-])=O

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 3 hits for monomerid = 50569231   

TargetCarbonic anhydrase 9(Homo sapiens (Human))TBA
LigandPNGBDBM50569231(CHEMBL4877663)copy SMILES
Affinity DataKi:  14nMAssay Description:Inhibition of human CA9 preincubated for 15 mins by phenol red dye based stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26H4N6QPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50569231(CHEMBL4877663)copy SMILES
Affinity DataKi:  44nMAssay Description:Inhibition of human CA2 preincubated for 15 mins by phenol red dye based stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26H4N6QPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50569231(CHEMBL4877663)copy SMILES
Affinity DataKi:  6.61E+3nMAssay Description:Inhibition of human CA1 preincubated for 15 mins by phenol red dye based stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26H4N6QPubMed