BDBM33266 CHEMBL379206::azo-sulfonamide, 1a::p-Phenyldiazenyl derivative, 5

SMILES NS(=O)(=O)c1ccc(cc1)N=Nc1ccc(O)cc1

InChI Key InChIKey=IPPFWRRJWLCWGK-UHFFFAOYSA-N

Data  9 KI  1 IC50

  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 4 hits for monomerid = 33266   

TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universita Degli Studi Di Firenze

LigandPNGBDBM33266(CHEMBL379206 | azo-sulfonamide, 1a | p-Phenyldiaze...)
Affinity DataKi:  5nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
Universita Degli Studi Di Firenze

LigandPNGBDBM33266(CHEMBL379206 | azo-sulfonamide, 1a | p-Phenyldiaze...)
Affinity DataKi:  6.40nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universita Degli Studi Di Firenze

LigandPNGBDBM33266(CHEMBL379206 | azo-sulfonamide, 1a | p-Phenyldiaze...)
Affinity DataKi:  393nM ΔG°:  -8.73kcal/molepH: 7.4 T: 2°CAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Universita Degli Studi Di Firenze

LigandPNGBDBM33266(CHEMBL379206 | azo-sulfonamide, 1a | p-Phenyldiaze...)
Affinity DataKi:  665nM ΔG°:  -8.42kcal/molepH: 7.4 T: 2°CAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed