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-1 angiotensin II receptor(Rabbit)
TBA

Curated by ChEMBL
LigandPNGBDBM50049195(L-162389 | 3-[(2'-(butylsulfonylcarbamate)-3'-prop...)
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 Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetType-2 angiotensin II receptor(Human)
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50049195(L-162389 | 3-[(2'-(butylsulfonylcarbamate)-3'-prop...)
Affinity DataIC50: 4.20nMAssay Description:Binding affinity towards Angiotensin II receptor, type 2 was measured through displacement of [125I]-Ang II in pig uterus myometrial membranesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetType-2 angiotensin II receptor(Human)
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50049195(L-162389 | 3-[(2'-(butylsulfonylcarbamate)-3'-prop...)
Affinity DataIC50: 4.20nMAssay Description:Binding affinity to AT2 receptor (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/4/2016
Entry Details Article
PubMed
TargetType-1 angiotensin II receptor(Human)
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50049195(L-162389 | 3-[(2'-(butylsulfonylcarbamate)-3'-prop...)
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 Depth
Date in BDB:
4/4/2016
Entry Details Article
PubMed
TargetType-2 angiotensin II receptor(Human)
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50049195(L-162389 | 3-[(2'-(butylsulfonylcarbamate)-3'-prop...)
Affinity DataIC50: 4.20nMAssay Description:Binding affinity to type-2 angiotensin-2 receptor (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/14/2017
Entry Details Article
PubMed
TargetType-2 angiotensin II receptor(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50049195(L-162389 | 3-[(2'-(butylsulfonylcarbamate)-3'-prop...)
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 Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetType-2 angiotensin II receptor(Human)
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50049195(L-162389 | 3-[(2'-(butylsulfonylcarbamate)-3'-prop...)
Affinity DataIC50: 6.10nMAssay Description:Inhibition of Angiotensin II receptor, type 2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetType-1 angiotensin II receptor(Human)
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50049195(L-162389 | 3-[(2'-(butylsulfonylcarbamate)-3'-prop...)
Affinity DataIC50: 1.5nMAssay Description:Inhibition of Angiotensin II receptor, type 1More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetType-2 angiotensin II receptor(Human)
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50049195(L-162389 | 3-[(2'-(butylsulfonylcarbamate)-3'-prop...)
Affinity DataKi:  1.5nMAssay Description:Binding affinity to angiotensin II receptor (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/30/2017
Entry Details Article
PubMed