BDBM50101822 (Z)-7-[(1R,2R,3R)-3-Hydroxy-2-((E)-(R)-3-hydroxy-oct-1-enyl)-5-oxo-cyclopentyl]-hept-5-enoic acid::CHEMBL64804::PGE2, 15-epi::US9180116, PGE2

SMILES: CCCCC[C@@H](O)\C=C\[C@H]1[C@H](O)CC(=O)[C@@H]1C\C=C/CCCC(O)=O

InChI Key: InChIKey=XEYBRNLFEZDVAW-UHFFFAOYSA-N

Data: 8 KI  1 IC50  5 EC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 13 hits for monomerid = 50101822   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Prostaglandin E2 receptor EP4 subtype (Human)	BDBM50101822 (CHEMBL64804 | PGE2, 15-epi | (Z)-7-[(1R,2R,3R)-3-H...) Show SMILES Show InChI	GoogleScholar	UniChem		n/a	n/a	n/a	n/a	0.480	n/a	n/a	n/a	37
TBA									Citation and Details
					More data for this Ligand-Target Pair
Prostaglandin E2 receptor EP4 subtype (Human)	BDBM50101822 (CHEMBL64804 | PGE2, 15-epi | (Z)-7-[(1R,2R,3R)-3-H...) Show SMILES Show InChI	GoogleScholar	UniChem		n/a	n/a	n/a	n/a	0.0500	n/a	n/a	n/a	37
TBA									Citation and Details
					More data for this Ligand-Target Pair
Prostaglandin E2 receptor EP2 subtype (Human)	BDBM50101822 (CHEMBL64804 | PGE2, 15-epi | (Z)-7-[(1R,2R,3R)-3-H...) Show SMILES Show InChI	GoogleScholar	UniChem		n/a	n/a	n/a	n/a	59	n/a	n/a	n/a	37
TBA									Citation and Details
					More data for this Ligand-Target Pair
Prostaglandin E2 receptor EP2 subtype (Mouse)	BDBM50101822 (CHEMBL64804 | PGE2, 15-epi | (Z)-7-[(1R,2R,3R)-3-H...) Show SMILES Show InChI	GoogleScholar	UniChem		n/a	n/a	n/a	n/a	2.10	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Prostacyclin receptor (Human)	BDBM50101822 (CHEMBL64804 | PGE2, 15-epi | (Z)-7-[(1R,2R,3R)-3-H...) Show SMILES Show InChI	GoogleScholar	UniChem		n/a	n/a	n/a	n/a	260	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Prostaglandin E2 receptor EP4 subtype (Human)	BDBM50101822 (CHEMBL64804 | PGE2, 15-epi | (Z)-7-[(1R,2R,3R)-3-H...) Show SMILES Show InChI	GoogleScholar	UniChem		0.140	n/a	0.380	n/a	n/a	n/a	n/a	6.0	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Prostaglandin E2 receptor EP4 subtype (Mouse)	BDBM50101822 (CHEMBL64804 | PGE2, 15-epi | (Z)-7-[(1R,2R,3R)-3-H...) Show SMILES Show InChI	GoogleScholar	UniChem		3.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Prostaglandin E2 receptor EP3 subtype (Mouse)	BDBM50101822 (CHEMBL64804 | PGE2, 15-epi | (Z)-7-[(1R,2R,3R)-3-H...) Show SMILES Show InChI	GoogleScholar	UniChem		5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Prostaglandin E2 receptor EP1 subtype (Mouse)	BDBM50101822 (CHEMBL64804 | PGE2, 15-epi | (Z)-7-[(1R,2R,3R)-3-H...) Show SMILES Show InChI	GoogleScholar	UniChem		18	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Prostaglandin E2 receptor EP2 subtype (Mouse)	BDBM50101822 (CHEMBL64804 | PGE2, 15-epi | (Z)-7-[(1R,2R,3R)-3-H...) Show SMILES Show InChI	GoogleScholar	UniChem		38	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Prostacyclin receptor (Human)	BDBM50101822 (CHEMBL64804 | PGE2, 15-epi | (Z)-7-[(1R,2R,3R)-3-H...) Show SMILES Show InChI	GoogleScholar	UniChem		>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Prostacyclin receptor (Mouse)	BDBM50101822 (CHEMBL64804 | PGE2, 15-epi | (Z)-7-[(1R,2R,3R)-3-H...) Show SMILES Show InChI	GoogleScholar	UniChem		>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Prostacyclin receptor (Human)	BDBM50101822 (CHEMBL64804 | PGE2, 15-epi | (Z)-7-[(1R,2R,3R)-3-H...) Show SMILES Show InChI	GoogleScholar	UniChem		>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair