BDBM50343660 4-((3,5-diamino-1H-pyrazol-4-yl)diazenyl)benzenesulfonamide::CHEMBL1775075

SMILES Nc1n[nH]c(N)c1\N=N\c1ccc(cc1)S(N)(=O)=O

InChI Key InChIKey=XLIZDMWIBNVIPS-BUHFOSPRSA-N

Data  4 KI  3 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 7 hits for monomerid = 50343660   

TargetCarbonic anhydrase 12(Homo sapiens (Human))
Egyptian Russian University

Curated by ChEMBL
LigandPNGBDBM50343660(4-((3,5-diamino-1H-pyrazol-4-yl)diazenyl)benzenesu...)
Affinity DataKi:  10nMAssay Description:Inhibition of recombinant human carbonic anhydrase 12 preincubated with enzyme for 15 mins by phenol red dye based stopped flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
Egyptian Russian University

Curated by ChEMBL
LigandPNGBDBM50343660(4-((3,5-diamino-1H-pyrazol-4-yl)diazenyl)benzenesu...)
Affinity DataKi:  22nMAssay Description:Inhibition of recombinant human carbonic anhydrase 9 preincubated with enzyme for 15 mins by phenol red dye based stopped flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Egyptian Russian University

Curated by ChEMBL
LigandPNGBDBM50343660(4-((3,5-diamino-1H-pyrazol-4-yl)diazenyl)benzenesu...)
Affinity DataKi:  38nMAssay Description:Inhibition of recombinant human carbonic anhydrase 2 preincubated with enzyme for 15 mins by phenol red dye based stopped flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Egyptian Russian University

Curated by ChEMBL
LigandPNGBDBM50343660(4-((3,5-diamino-1H-pyrazol-4-yl)diazenyl)benzenesu...)
Affinity DataKi:  271nMAssay Description:Inhibition of recombinant human carbonic anhydrase 1 preincubated with enzyme for 15 mins by phenol red dye based stopped flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-T1/Cyclin-dependent kinase 9(Homo sapiens (Human))
Egyptian Russian University

Curated by ChEMBL
LigandPNGBDBM50343660(4-((3,5-diamino-1H-pyrazol-4-yl)diazenyl)benzenesu...)
Affinity DataIC50: >1.25E+4nMAssay Description:Inhibition of human full-length N-terminal GST/His6-tagged CDK9 (1 to 372 residues)/His6-tagged Cyclin-T1 (1 to 726 residues) expressed in sf9 cells ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRibosomal protein S6 kinase alpha-3(Homo sapiens (Human))
East China University Of Science And Technology

Curated by ChEMBL
LigandPNGBDBM50343660(4-((3,5-diamino-1H-pyrazol-4-yl)diazenyl)benzenesu...)
Affinity DataIC50:  5.50E+3nMAssay Description:Inhibition of RSK2 after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Homo sapiens (Human))
Egyptian Russian University

Curated by ChEMBL
LigandPNGBDBM50343660(4-((3,5-diamino-1H-pyrazol-4-yl)diazenyl)benzenesu...)
Affinity DataIC50:  4.17E+4nMAssay Description:Inhibition of CDK2/cyclin E (unknown origin) expressed in baculovirus infected Sf21 insect cells using histone H1 as substrate in presence of [gamma3...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed