null

SMILES CC(C)N(CC[C@H](c1ccccc1)c1cc(CCCCOc2ccc(CCNC[C@H](O)c3ccc(O)c(O)c3)cc2)ccc1O)C(C)C

InChI Key InChIKey=DORKQDJVMZQKPG-ABJZOGFOSA-N

  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 2 hits for monomerid = 50343159   

TargetMuscarinic acetylcholine receptor M3(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50343159(4-((R)-2-(4-(4-(3-((R)-3-(diisopropylamino)-1-phen...)copy SMILEScopy InChI
Affinity DataKi:  4.70nMAssay Description:Displacement of [3H]N-methyl Scopolamine from human muscarinic M3 receptor expressed in CHO cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G73F1BPubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50343159(4-((R)-2-(4-(4-(3-((R)-3-(diisopropylamino)-1-phen...)copy SMILEScopy InChI
Affinity DataEC50:  173nMAssay Description:Agonist activity at human beta2 adrenergic receptor expressed in CHO cells assessed as stimulation of intracellular cAMP production after 30 mins of ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G73F1BPubMed