BDBM50196205 2-(benzo[c][1,2,5]thiadiazole-4-sulfonamido)-N-benzyl-4-chlorobenzamide::2-[(2,1,3-benzothiadiazol-4-ylsulfonyl)amino]-4-chloro-N-(phenylmethyl)-benzamide::CHEMBL217492

SMILES Clc1ccc(C(=O)NCc2ccccc2)c(NS(=O)(=O)c2cccc3nsnc23)c1

InChI Key InChIKey=DGXZODRYVWWLTN-UHFFFAOYSA-N

Data  3 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 3 hits for monomerid = 50196205   

TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50196205(2-(benzo[c][1,2,5]thiadiazole-4-sulfonamido)-N-ben...)
Affinity DataKi:  2.51E+3nMAssay Description:Displacement of [125I]-CCK-8S from CCK2R after 100 mins by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholecystokinin receptor type A(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50196205(2-(benzo[c][1,2,5]thiadiazole-4-sulfonamido)-N-ben...)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [125I]-CCK-8S from CCK1R after 100 mins by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholecystokinin receptor type A(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50196205(2-(benzo[c][1,2,5]thiadiazole-4-sulfonamido)-N-ben...)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [125I]CCK-8S from human CCK1RMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed