BDBM50001363 (1R-enantiomer)7,7-dimethyl-1-spiro[2,3-dihydro-1H-indene-1,4'-(hexahydropyridine)]-1-ylsulfonylmethyl-(1S,4R)-bicyclo[2.2.1]heptan-2-one::CHEMBL129268

SMILES CC1(C)C2CC[C@@]1(CS(=O)(=O)N1CCC3(CCc4ccccc34)CC1)C(=O)C2

InChI Key InChIKey=XEGCBPWQNYJXLN-WBPHRXDCSA-N

Data  3 IC50

  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 3 hits for monomerid = 50001363   

TargetOxytocin receptor(RAT)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50001363((1R-enantiomer)7,7-dimethyl-1-spiro[2,3-dihydro-1H...)
Affinity DataIC50:  1.10E+3nMAssay Description:Half-maximal inhibition of binding of [3H]-Oxytocin to OT receptor in rat uterine tissueMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVasopressin V1a/V1b/V2 receptor(RAT)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50001363((1R-enantiomer)7,7-dimethyl-1-spiro[2,3-dihydro-1H...)
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 DepthDetails ArticlePubMed
TargetVasopressin V1a/V1b/V2 receptor(RAT)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50001363((1R-enantiomer)7,7-dimethyl-1-spiro[2,3-dihydro-1H...)
Affinity DataIC50: >1.00E+4nMAssay Description:Half-maximal inhibition of binding of [3H]vasopressin to vasopressin receptor 1 in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed