BDBM50049195 3-[(2'-(butylsulfonylcarbamate)-3'-propyl-1,1'-biphenyl-4-yl)methyl]-2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine::4'-(2-Ethyl-57-dimethyl-imidazo[45-b]pyridin-3-ylmethyl)-5-propyl-biphenyl-2-sulfonic acid butyloxycarbonylamide(L-162389)::CHEMBL39959::L-162389::N-Butyloxycarbonyl-4'-(2-Ethyl-5,7-dimethyl-imidazo[4,5-b]pyridin-3-ylmethyl)-5-propyl-biphenyl-2-sulfonic acid amide

SMILES CCCCOC(=O)NS(=O)(=O)c1ccc(CCC)cc1-c1ccc(Cn2c(CC)nc3c(C)cc(C)nc23)cc1

InChI Key InChIKey=MLGCITBDCGSKQS-UHFFFAOYSA-N

Data  1 KI  8 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 9 hits for monomerid = 50049195   

TargetType-2 angiotensin II receptor(Homo sapiens (Human))
University Of Minnesota

Curated by ChEMBL
LigandPNGBDBM50049195(3-[(2'-(butylsulfonylcarbamate)-3'-propyl-1,1'-bip...)
Affinity DataKi:  1.5nMAssay Description:Inhibition of KDM5B (unknown origin) using biotin-H3K4me3 as substrate preincubated for 15 mins followed by substrate addition measured after 20 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetType-2 angiotensin II receptor(Homo sapiens (Human))
University Of Minnesota

Curated by ChEMBL
LigandPNGBDBM50049195(3-[(2'-(butylsulfonylcarbamate)-3'-propyl-1,1'-bip...)
Affinity DataIC50:  4.20nMAssay Description:Binding affinity of the compound towards Angiotensin II receptor, type 2 was measured through displacement of [125I]-Ang II in pig uterus myometrial ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetType-2 angiotensin II receptor(Homo sapiens (Human))
University Of Minnesota

Curated by ChEMBL
LigandPNGBDBM50049195(3-[(2'-(butylsulfonylcarbamate)-3'-propyl-1,1'-bip...)
Affinity DataIC50:  4.20nMAssay Description:Binding affinity to AT2 receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetType-1 angiotensin II receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50049195(3-[(2'-(butylsulfonylcarbamate)-3'-propyl-1,1'-bip...)
Affinity DataIC50:  1.5nMAssay Description:Displacement of [125I]-[Sar1,Leu8]angiotensin II from human AT1 receptor expressed in african green monkey COS7 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetType-1 angiotensin II receptor(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50049195(3-[(2'-(butylsulfonylcarbamate)-3'-propyl-1,1'-bip...)
Affinity DataIC50:  1.5nMAssay Description:Inhibition of Angiotensin II receptor, type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetType-2 angiotensin II receptor(RAT)
TBA

Curated by ChEMBL
LigandPNGBDBM50049195(3-[(2'-(butylsulfonylcarbamate)-3'-propyl-1,1'-bip...)
Affinity DataIC50:  3.80nMAssay Description:Compound was evaluated for inhibition of 125I[Sar1,Ile8] aII binding to rat midbrain membrane preparation Angiotensin II receptor, type 2More data for this Ligand-Target Pair
In DepthDetails Article
TargetType-2 angiotensin II receptor(Homo sapiens (Human))
University Of Minnesota

Curated by ChEMBL
LigandPNGBDBM50049195(3-[(2'-(butylsulfonylcarbamate)-3'-propyl-1,1'-bip...)
Affinity DataIC50:  6.10nMAssay Description:Inhibition of Angiotensin II receptor, type 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetType-1 angiotensin II receptor(RABBIT)
TBA

Curated by ChEMBL
LigandPNGBDBM50049195(3-[(2'-(butylsulfonylcarbamate)-3'-propyl-1,1'-bip...)
Affinity DataIC50:  2.10nMAssay Description:Compound was evaluated for inhibition of 125I[Sar1,Ile8] all binding to rabbit aorta Angiotensin II receptor, type 1More data for this Ligand-Target Pair
In DepthDetails Article
TargetType-2 angiotensin II receptor(Homo sapiens (Human))
University Of Minnesota

Curated by ChEMBL
LigandPNGBDBM50049195(3-[(2'-(butylsulfonylcarbamate)-3'-propyl-1,1'-bip...)
Affinity DataIC50:  4.20nMAssay Description:Binding affinity to type-2 angiotensin-2 receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed