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Compile Data Set for Download or QSAR

Found 4 hits Enz. Inhib. hit(s) with Target = 'Prostaglandin E2 receptor EP3 subtype' and Ligand = 'BDBM50303670'   
Target/Host
(Institution)
LigandTarget/Host
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 EP3 subtype


(Homo sapiens (Human))
BDBM50303670
PNG
((2E)-3-[1-(2,4-dichlorobenzyl)-2-oxo-1,2-dihydrosp...)
Show SMILES Clc1cc(sc1Cl)S(=O)(=O)NC(=O)\C=C\c1cccc2c1N(Cc1ccc(Cl)cc1Cl)C(=O)C21NCCS1
Show InChI InChI=1S/C24H17Cl4N3O4S3/c25-15-6-4-14(17(26)10-15)12-31-21-13(2-1-3-16(21)24(23(31)33)29-8-9-36-24)5-7-19(32)30-38(34,35)20-11-18(27)22(28)37-20/h1-7,10-11,29H,8-9,12H2,(H,30,32)/b7-5+
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Article
PubMed
n/an/a 4.90n/an/an/an/an/an/a



deCODE Chemistry, Inc.

Curated by ChEMBL


Assay Description
Displacement of [3H]PGE2 from human EP3 receptor after 1 hr by liquid scintillation counting


J Med Chem 53: 18-36 (2010)


Article DOI: 10.1021/jm9005912
BindingDB Entry DOI: 10.7270/Q2XP752H
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor EP3 subtype


(Homo sapiens (Human))
BDBM50303670
PNG
((2E)-3-[1-(2,4-dichlorobenzyl)-2-oxo-1,2-dihydrosp...)
Show SMILES Clc1cc(sc1Cl)S(=O)(=O)NC(=O)\C=C\c1cccc2c1N(Cc1ccc(Cl)cc1Cl)C(=O)C21NCCS1
Show InChI InChI=1S/C24H17Cl4N3O4S3/c25-15-6-4-14(17(26)10-15)12-31-21-13(2-1-3-16(21)24(23(31)33)29-8-9-36-24)5-7-19(32)30-38(34,35)20-11-18(27)22(28)37-20/h1-7,10-11,29H,8-9,12H2,(H,30,32)/b7-5+
PDB

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UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 4.90n/an/an/an/an/an/a



deCODE Chemistry

Curated by ChEMBL


Assay Description
Displacement of [3H]PGE2 from human EP3 receptor in buffer


Bioorg Med Chem Lett 20: 2658-64 (2010)


Article DOI: 10.1016/j.bmcl.2010.02.028
BindingDB Entry DOI: 10.7270/Q2668DCG
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor EP3 subtype


(Homo sapiens (Human))
BDBM50303670
PNG
((2E)-3-[1-(2,4-dichlorobenzyl)-2-oxo-1,2-dihydrosp...)
Show SMILES Clc1cc(sc1Cl)S(=O)(=O)NC(=O)\C=C\c1cccc2c1N(Cc1ccc(Cl)cc1Cl)C(=O)C21NCCS1
Show InChI InChI=1S/C24H17Cl4N3O4S3/c25-15-6-4-14(17(26)10-15)12-31-21-13(2-1-3-16(21)24(23(31)33)29-8-9-36-24)5-7-19(32)30-38(34,35)20-11-18(27)22(28)37-20/h1-7,10-11,29H,8-9,12H2,(H,30,32)/b7-5+
PDB

KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 880n/an/an/an/an/an/a



deCODE Chemistry

Curated by ChEMBL


Assay Description
Displacement of [3H]PGE2 from human EP3 receptor in presence of 10% human serum


Bioorg Med Chem Lett 20: 2658-64 (2010)


Article DOI: 10.1016/j.bmcl.2010.02.028
BindingDB Entry DOI: 10.7270/Q2668DCG
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor EP3 subtype


(Homo sapiens (Human))
BDBM50303670
PNG
((2E)-3-[1-(2,4-dichlorobenzyl)-2-oxo-1,2-dihydrosp...)
Show SMILES Clc1cc(sc1Cl)S(=O)(=O)NC(=O)\C=C\c1cccc2c1N(Cc1ccc(Cl)cc1Cl)C(=O)C21NCCS1
Show InChI InChI=1S/C24H17Cl4N3O4S3/c25-15-6-4-14(17(26)10-15)12-31-21-13(2-1-3-16(21)24(23(31)33)29-8-9-36-24)5-7-19(32)30-38(34,35)20-11-18(27)22(28)37-20/h1-7,10-11,29H,8-9,12H2,(H,30,32)/b7-5+
PDB

KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 880n/an/an/an/an/an/a



deCODE Chemistry, Inc.

Curated by ChEMBL


Assay Description
Displacement of [3H]PGE2 from human EP3 receptor after 1 hr by liquid scintillation counting in presence of 10% human serum


J Med Chem 53: 18-36 (2010)


Article DOI: 10.1021/jm9005912
BindingDB Entry DOI: 10.7270/Q2XP752H
More data for this
Ligand-Target Pair