null

SMILES CCOC(=O)C1=C(C2OC1C=C2[C@@H]1C[C@@]2(C)[C@@H](CC[C@@]3(C)[C@@H](C[C@H](OC(C)=O)C(=O)[C@H]23)C(=O)OC)C(=O)O1)C(=O)OCC

InChI Key InChIKey=CMQQVVSHAASTRM-NRJGBIRPSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50343252   

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

Curated by ChEMBL
LigandPNGBDBM50343252(CHEMBL1773747 | Diethyl 5-((2S,4aR,6aR,7R,9S,10aS,...)copy SMILEScopy InChI
Affinity DataKi:  120nMAssay Description:Displacement of [3H]U69593 from kappa opioid receptorMore 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
LigandPNGBDBM50343252(CHEMBL1773747 | Diethyl 5-((2S,4aR,6aR,7R,9S,10aS,...)copy SMILEScopy InChI
Affinity DataKi:  2.26E+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
TargetMu-type opioid receptor(Homo sapiens (Human))
University of Iowa

Curated by ChEMBL
LigandPNGBDBM50343252(CHEMBL1773747 | Diethyl 5-((2S,4aR,6aR,7R,9S,10aS,...)copy SMILEScopy InChI
Affinity DataKi: >3.20E+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