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Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Prostaglandin E2 receptor EP4 subtype' AND taxid = 9986   
Target
(Institution)
LigandTarget
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Prostaglandin E2 receptor EP4 subtype


(Oryctolagus cuniculus)
BDBM50359616
PNG
(CHEMBL1928221)
Show SMILES O[C@@H](CC1CCCCC1)\C=C\[C@H]1[C@H](O)C[C@@H]2Oc3c(cccc3CCC(O)=O)[C@H]12
Show InChI InChI=1S/C24H32O5/c25-17(13-15-5-2-1-3-6-15)10-11-18-20(26)14-21-23(18)19-8-4-7-16(24(19)29-21)9-12-22(27)28/h4,7-8,10-11,15,17-18,20-21,23,25-26H,1-3,5-6,9,12-14H2,(H,27,28)/b11-10+/t17-,18+,20-,21+,23+/m1/s1
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

AffyNet 
Article
PubMed
n/an/an/an/a 5.70n/an/an/an/a



Toray Industries, Inc.

Curated by ChEMBL


Assay Description
Agonist activity at rabbit EP4 receptor assessed as relaxation of Kcl-induced tissue contraction by isometric transducer method


Citation and Details
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor EP4 subtype


(Oryctolagus cuniculus)
BDBM50359615
PNG
(CHEMBL1928220)
Show SMILES O[C@@H](CC1CCCCC1)\C=C\[C@H]1[C@H](O)C[C@@H]2Oc3c(cccc3CCc3nnn[nH]3)[C@H]12
Show InChI InChI=1S/C24H32N4O3/c29-17(13-15-5-2-1-3-6-15)10-11-18-20(30)14-21-23(18)19-8-4-7-16(24(19)31-21)9-12-22-25-27-28-26-22/h4,7-8,10-11,15,17-18,20-21,23,29-30H,1-3,5-6,9,12-14H2,(H,25,26,27,28)/b11-10+/t17-,18+,20-,21+,23+/m1/s1
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents

AffyNet 
Article
PubMed
n/an/an/an/a 2.60n/an/an/an/a



Toray Industries, Inc.

Curated by ChEMBL


Assay Description
Agonist activity at rabbit EP4 receptor assessed as relaxation of Kcl-induced tissue contraction by isometric transducer method


Citation and Details
More data for this
Ligand-Target Pair