BDBM50001411 (1S-enantiomer)1-(4,4-diphenylhexahydro-1-pyridinylsulfonylmethyl)-7,7-dimethyl-(1S,4R)-bicyclo[2.2.1]heptan-2-one::CHEMBL126025

SMILES CC1(C)C2CC[C@@]1(CS(=O)(=O)N1CCC(CC1)(c1ccccc1)c1ccccc1)C(=O)C2

InChI Key InChIKey=RUAKAZIVMTZJIV-UHFFFAOYSA-N

Data  3 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 3 hits for monomerid = 50001411   

TargetOxytocin receptor(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50001411(CHEMBL126025 | (1S-enantiomer)1-(4,4-diphenylhexah...)
Affinity DataIC50: 1.00E+4nMAssay Description:Half-maximal inhibition of binding of [3H]oxytocin to OT receptor in rat uterine tissueMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVasopressin V1a/V1b/V2 receptor(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50001411(CHEMBL126025 | (1S-enantiomer)1-(4,4-diphenylhexah...)
Affinity DataIC50: 1.00E+4nMAssay Description:Half-maximal inhibition of binding of [3H]- vasopressin to the vasopressin receptor 2 in rat kidneyMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVasopressin V1a/V1b/V2 receptor(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50001411(CHEMBL126025 | (1S-enantiomer)1-(4,4-diphenylhexah...)
Affinity DataIC50: 1.00E+5nMAssay Description:Half-maximal inhibition of binding of [3H]vasopressin to vasopressin receptor 1 in rat liverMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed