BDBM50329822 5-[(2-Benzyl-1H-benzimidazol-1-yl)acetyl]-2-chlorobenzenesulfonamide::CHEMBL1272242::N-alkylated benzimidazole derivative, 4d::carbonic anhydrase (CA) inhibitors, benzenesulphonamide ligand, 5

SMILES NS(=O)(=O)c1cc(ccc1Cl)C(=O)Cn1c(Cc2ccccc2)nc2ccccc12

InChI Key InChIKey=UUAIBIWLOHLXLK-UHFFFAOYSA-N

Data  23 Kd  8 Koff  4 Kon

  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 = 50329822   

TargetCarbonic anhydrase 12(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50329822(5-[(2-Benzyl-1H-benzimidazol-1-yl)acetyl]-2-chloro...)
Affinity DataKoff:  1.00E+5s-1Assay Description:Binding affinity to human recombinant CA12 catalytic domain assessed as association rate constant after 30 secs by surface plasmon resonance assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50329822(5-[(2-Benzyl-1H-benzimidazol-1-yl)acetyl]-2-chloro...)
Affinity DataKd:  769nMpH: 7.0Assay Description:The thermal shift assay (TSA) measurements were performed in a Corbett Rotor-Gene 6000 (QIAGEN Rotor-Gene Q, Sydney, Australia) instrument using the ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50329822(5-[(2-Benzyl-1H-benzimidazol-1-yl)acetyl]-2-chloro...)
Affinity DataKon:  0.0200M-1s-1Assay Description:Binding affinity to human recombinant CA12 catalytic domain assessed as dissociation rate constant after 30 secs by surface plasmon resonance assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50329822(5-[(2-Benzyl-1H-benzimidazol-1-yl)acetyl]-2-chloro...)
Affinity DataKd:  200nMAssay Description:Binding affinity to human recombinant CA12 catalytic domain after 30 secs by surface plasmon resonance assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50329822(5-[(2-Benzyl-1H-benzimidazol-1-yl)acetyl]-2-chloro...)
Affinity DataKd:  370nMAssay Description:Binding affinity to human recombinant CA12 catalytic domain by fluorescence-based thermal shift assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50329822(5-[(2-Benzyl-1H-benzimidazol-1-yl)acetyl]-2-chloro...)
Affinity DataKd:  1.60nMAssay Description:Inhibition of Topoisomerase I by cleavage complex formation in intact human HL-60 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50329822(5-[(2-Benzyl-1H-benzimidazol-1-yl)acetyl]-2-chloro...)
Affinity DataKon:  0.0200M-1s-1Assay Description:Binding affinity to CA12 (unknown origin) assessed as dissociation rate constant at pH 7 by SPR assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed