BDBM50021253 7alpha-[(1R)-1-Hydroxy1-methyl-3-[4-[3-(bromomercurio)-2-methoxypropoxy]phenyl]-6,14-endo-ethenotetrahydrothebaine]::CHEMBL58589

SMILES COC(COc1ccc(CC[C@](C)(O)[C@H]2C[C@]34C=C[C@]2(OC)[C@@H]2Oc5c6c(CC3N(C)CCC426)ccc5OC)cc1)C[Hg]Br

InChI Key InChIKey=FLMYZKLRQCJYRQ-UHFFFAOYSA-M

Data  2 IC50

  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 2 hits for monomerid = 50021253   

TargetDelta-type opioid receptor(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50021253(CHEMBL58589 | 7alpha-[(1R)-1-Hydroxy1-methyl-3-[4-...)
Affinity DataIC50: 250nMAssay Description:Evaluated for the inhibition of [3H]DADLE binding to Opioid receptor delta 1 in rat brain homogenates.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/13/2012
Entry Details Article
PubMed
TargetMu-type opioid receptor(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50021253(CHEMBL58589 | 7alpha-[(1R)-1-Hydroxy1-methyl-3-[4-...)
Affinity DataIC50: 95nMAssay Description:Evaluated for the inhibition of [3H]naltrexone binding to Opioid receptor mu 1 in rat brain homogenates.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/13/2012
Entry Details Article
PubMed