BDBM50001416 (1S-enantiomer)7,7-dimethyl-1-[3'-phenylspiro[1H-indene-1,4'-(hexahydropyridine)]-1-ylsulfonylmethyl]-(1S,4R)-bicyclo[2.2.1]heptan-2-one::CHEMBL126708

SMILES CC1(C)C2CC[C@@]1(CS(=O)(=O)N1CCC3(C=Cc4ccccc34)C(C1)c1ccccc1)C(=O)C2

InChI Key InChIKey=WIVGUQZLSVDYBV-UWSKJBMKSA-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 = 50001416   

TargetOxytocin receptor(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50001416((1S-enantiomer)7,7-dimethyl-1-[3'-phenylspiro[1H-i...)
Affinity DataIC50:  8.50E+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
LigandPNGBDBM50001416((1S-enantiomer)7,7-dimethyl-1-[3'-phenylspiro[1H-i...)
Affinity DataIC50:  790nMAssay 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
TargetVasopressin V1a/V1b/V2 receptor(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50001416((1S-enantiomer)7,7-dimethyl-1-[3'-phenylspiro[1H-i...)
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