BDBM50403949 CHEMBL2112332

SMILES C(Cc1ccccc1)SCc1ccc(cc1)-c1ccccc1CCc1nnn[nH]1

InChI Key InChIKey=RAOXWVJENLEGBP-UHFFFAOYSA-N

Data  4 KI

  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 4 hits for monomerid = 50403949   

TargetProstaglandin E2 receptor EP2 subtype(Human)
Merck Frosst Centre For Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50403949(CHEMBL2112332)
Affinity DataKi:  63nMAssay Description:Binding affinity at human Prostanoid EP2 receptor.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProstaglandin E2 receptor EP3 subtype(Human)
Merck Frosst Centre For Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50403949(CHEMBL2112332)
Affinity DataKi:  1.00E+3nMAssay Description:Binding affinity at human Prostanoid EP3 receptor.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProstaglandin E2 receptor EP4 subtype(Human)
Merck Frosst Centre For Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50403949(CHEMBL2112332)
Affinity DataKi:  2.60E+3nMAssay Description:Binding affinity at human Prostanoid EP4 receptor.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProstaglandin E2 receptor EP1 subtype(Human)
Merck Frosst Centre For Therapeutic Research

Curated by ChEMBL
LigandPNGBDBM50403949(CHEMBL2112332)
Affinity DataKi:  4.90E+3nMAssay Description:Binding affinity at human Prostanoid EP1 receptor.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed