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Compile Data Set for Download or QSAR

Marvin 2D Structure

The following exact ligands are found in BindingDB

Wt: 525.5
BDBM50027881

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB (change energy unit to kcal/mol)

Found 2 hits in this display   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Beta-2 adrenergic receptor


(Homo sapiens (Human))
BDBM50027881
PNG
(CHEMBL2348207)
Show SMILES OC(CNCCNC(=O)Nc1cccc(c1)C(F)(F)F)COc1ccc(OCCOC2CCCC2)cc1
Show InChI InChI=1S/C26H34F3N3O5/c27-26(28,29)19-4-3-5-20(16-19)32-25(34)31-13-12-30-17-21(33)18-37-24-10-8-23(9-11-24)36-15-14-35-22-6-1-2-7-22/h3-5,8-11,16,21-22,30,33H,1-2,6-7,12-15,17-18H2,(H2,31,32,34)
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Article
PubMed
n/an/an/a 1.38E+3n/an/an/an/an/a



University of Nottingham

Curated by ChEMBL


Assay Description
Displacement of [3H]-CGP12177 from human beta2 adrenoceptor expressed in CHOK1 cells after 2 hrs by scintillation counting analysis


J Med Chem 56: 3852-65 (2013)


Article DOI: 10.1021/jm400348g
BindingDB Entry DOI: 10.7270/Q2445NV6
More data for this
Ligand-Target Pair
Beta-1 adrenergic receptor


(Homo sapiens (Human))
BDBM50027881
PNG
(CHEMBL2348207)
Show SMILES OC(CNCCNC(=O)Nc1cccc(c1)C(F)(F)F)COc1ccc(OCCOC2CCCC2)cc1
Show InChI InChI=1S/C26H34F3N3O5/c27-26(28,29)19-4-3-5-20(16-19)32-25(34)31-13-12-30-17-21(33)18-37-24-10-8-23(9-11-24)36-15-14-35-22-6-1-2-7-22/h3-5,8-11,16,21-22,30,33H,1-2,6-7,12-15,17-18H2,(H2,31,32,34)
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/an/a 17n/an/an/an/an/a



University of Nottingham

Curated by ChEMBL


Assay Description
Displacement of [3H]-CGP12177 from human beta1 adrenoceptor expressed in CHOK1 cells after 2 hrs by scintillation counting analysis


J Med Chem 56: 3852-65 (2013)


Article DOI: 10.1021/jm400348g
BindingDB Entry DOI: 10.7270/Q2445NV6
More data for this
Ligand-Target Pair