null

SMILES Cc1cc2CC(Cc2cc1C)NC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12

InChI Key InChIKey=PWAAGHQFYYZZAX-FQEVSTJZSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50318160   

TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50318160(8-Hydroxy-5-[(R)-1-hydroxy-2-(5,6-dimethylindan-2-...)copy SMILEScopy InChI
Affinity DataKi:  522nMAssay Description:Displacement of [125I]cyanopindolol from human recombinant beta2 adrenergic receptor expressed in CHO cells by filtration assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1JRTPubMed
TargetBeta-2 adrenergic receptor(GUINEA PIG)
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50318160(8-Hydroxy-5-[(R)-1-hydroxy-2-(5,6-dimethylindan-2-...)copy SMILEScopy InChI
Affinity DataIC50: 48nMAssay Description:Agonist activity at beta2 adrenergic receptor in guinea pig tracheal strip assessed as inhibition of electrically-induced bronchocontractile response...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1JRTPubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Novartis Institutes for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50318160(8-Hydroxy-5-[(R)-1-hydroxy-2-(5,6-dimethylindan-2-...)copy SMILEScopy InChI
Affinity DataEC50:  39nMAssay Description:Agonist activity at human beta2 adrenergic receptor assessed as increase in cAMP level by whole cell assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1JRTPubMed