null

SMILES COC(=O)[C@@H]1C[C@H](OC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@@H](C[C@]21C)C1=CC2OC1C1C3OC(C21)c1c3c2ccccc2c(=O)c2ccccc12

InChI Key InChIKey=RWHDALCENIBPKK-MCOKYAIJSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50343255   

TargetMu-type opioid receptor(Homo sapiens (Human))
University of Iowa

Curated by ChEMBL
LigandPNGBDBM50343255((2S,4aR,6aR,7R,9S,10aS,10bR)-Methyl 9-acetoxy-2-(8...)copy SMILEScopy InChI
Affinity DataKi: >2.70E+3nMAssay Description:Agonist activity at mu opioid receptor assessed as stimulation of [35S]GTPgammaS bindingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7W9VPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University of Iowa

Curated by ChEMBL
LigandPNGBDBM50343255((2S,4aR,6aR,7R,9S,10aS,10bR)-Methyl 9-acetoxy-2-(8...)copy SMILEScopy InChI
Affinity DataKi: >5.20E+3nMAssay Description:Displacement of [3H]DADLE from delta opioid receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7W9VPubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
University of Iowa

Curated by ChEMBL
LigandPNGBDBM50343255((2S,4aR,6aR,7R,9S,10aS,10bR)-Methyl 9-acetoxy-2-(8...)copy SMILEScopy InChI
Affinity DataKi: >1.30E+4nMAssay Description:Displacement of [3H]U69593 from kappa opioid receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7W9VPubMed