BDBM50394644 CHEMBL2164612

SMILES COc1cc(C\C=C\c2ccccc2\C=C\C(O)=O)ccc1OCC[n+]1c(C)cc(\C=C\C=C\c2ccc(cc2)N(C)C)cc1C

InChI Key InChIKey=YDEXMGGWTNDKSL-UHFFFAOYSA-O

Data  4 KI

  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 4 hits for monomerid = 50394644   

LigandPNGBDBM50394644(CHEMBL2164612)
Affinity DataKi:  135nMAssay Description:Displacement of [3H]PGE2 from human EP3R expressed in chem1 cells after 2hrs by beta countingMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
LigandPNGBDBM50394644(CHEMBL2164612)
Affinity DataKi:  902nMAssay Description:Displacement of [3H]PGE2 from human EP4R expressed in chem1 cells after 2hrs by beta countingMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
LigandPNGBDBM50394644(CHEMBL2164612)
Affinity DataKi:  2.94E+3nMAssay Description:Displacement of [3H]PGE2 from human EP2R expressed in chem1 cells after 2hrs by beta countingMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
LigandPNGBDBM50394644(CHEMBL2164612)
Affinity DataKi:  6.86E+4nMAssay Description:Displacement of [3H]PGE2 from human EP1R expressed in chem1 cells after 2hrs by beta countingMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed