BDBM50344556 4-(nitrooxy)butyl 4-(N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)sulfamoyl)benzoate::CHEMBL1778435

SMILES NS(=O)(=O)c1nnc(NS(=O)(=O)c2ccc(cc2)C(=O)OCCCCO[N+]([O-])=O)s1

InChI Key InChIKey=OCFUQFUKHCFTNG-UHFFFAOYSA-N

Data  5 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50344556   

TargetCarbonic anhydrase 2(Homo sapiens (Human))
U.O. Oculistica Az. Usl 3

Curated by ChEMBL
LigandPNGBDBM50344556(4-(nitrooxy)butyl 4-(N-(5-sulfamoyl-1,3,4-thiadiaz...)
Affinity DataKi:  10nMAssay Description:Inhibition of human CA2 by CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
U.O. Oculistica Az. Usl 3

Curated by ChEMBL
LigandPNGBDBM50344556(4-(nitrooxy)butyl 4-(N-(5-sulfamoyl-1,3,4-thiadiaz...)
Affinity DataKi:  10nMAssay Description:Inhibition of human recombinant CA9 catalytic domain by CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
U.O. Oculistica Az. Usl 3

Curated by ChEMBL
LigandPNGBDBM50344556(4-(nitrooxy)butyl 4-(N-(5-sulfamoyl-1,3,4-thiadiaz...)
Affinity DataKi:  31nMAssay Description:Inhibition of human recombinant CA12 catalytic domain by CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
U.O. Oculistica Az. Usl 3

Curated by ChEMBL
LigandPNGBDBM50344556(4-(nitrooxy)butyl 4-(N-(5-sulfamoyl-1,3,4-thiadiaz...)
Affinity DataKi:  32nMAssay Description:Inhibition of human CA1 by CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 4(Homo sapiens (Human))
U.O. Oculistica Az. Usl 3

Curated by ChEMBL
LigandPNGBDBM50344556(4-(nitrooxy)butyl 4-(N-(5-sulfamoyl-1,3,4-thiadiaz...)
Affinity DataKi:  46nMAssay Description:Inhibition of human CA4 by CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed