Compile Data Set for Download or QSAR
Report error Found 245 Enz. Inhib. hit(s) with all data for entry = 50038889
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295535BDBM50295535(1-butyl-N-(2,3-dimethoxybenzyl)-2-(3,4,5-trimethox...)
Affinity DataIC50: 1nMAssay Description:Inhibition of human sEH in HEK293 cells assessed as conversion of 14,15-epoxyeicosatrienoic acid to 14,15-dihydroepoxyeicosatrienoic acidMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 25737BDBM25737(12-[(adamantan-1-ylcarbamoyl)amino]dodecanoic acid...)
Affinity DataIC50: 1.60nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295541BDBM50295541(4-(3-(4-(methylsulfonyl)phenyl)-1,2,4-oxadiazol-5-...)
Affinity DataIC50: 4nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 25737BDBM25737(12-[(adamantan-1-ylcarbamoyl)amino]dodecanoic acid...)
Affinity DataIC50: 5nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295542BDBM50295542(4-(5-(1-(2-phenylcyclopropylcarbamoyl)piperidin-4-...)
Affinity DataIC50: 5nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295540BDBM50295540(N-(2-phenylcyclopropyl)-4-(3-(2-(trifluoromethyl)p...)
Affinity DataIC50: 6nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Mouse)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 25737BDBM25737(12-[(adamantan-1-ylcarbamoyl)amino]dodecanoic acid...)
Affinity DataIC50: 7nMAssay Description:Inhibition of mouse sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295548BDBM50295548(N-(2-phenylcyclopropyl)-4-(3-(quinolin-2-yl)-1,2,4...)
Affinity DataIC50: 7nMAssay Description:Inhibition of human sEH in HEK293 cells assessed as conversion of 14,15-epoxyeicosatrienoic acid to 14,15-dihydroepoxyeicosatrienoic acidMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295549BDBM50295549(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(4-(tr...)
Affinity DataIC50: 7nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295540BDBM50295540(N-(2-phenylcyclopropyl)-4-(3-(2-(trifluoromethyl)p...)
Affinity DataIC50: 7nMAssay Description:Inhibition of human sEH in HEK293 cells assessed as conversion of 14,15-epoxyeicosatrienoic acid to 14,15-dihydroepoxyeicosatrienoic acidMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295549BDBM50295549(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(4-(tr...)
Affinity DataIC50: 7nMAssay Description:Inhibition of human sEH in HEK293 cells assessed as conversion of 14,15-epoxyeicosatrienoic acid to 14,15-dihydroepoxyeicosatrienoic acidMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295548BDBM50295548(N-(2-phenylcyclopropyl)-4-(3-(quinolin-2-yl)-1,2,4...)
Affinity DataIC50: 7nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295543BDBM50295543(N-(2-phenylcyclopropyl)-4-(3-(pyridin-3-yl)-1,2,4-...)
Affinity DataIC50: 7nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295539BDBM50295539(4-(benzo[d]oxazol-2-yl)-N-(2-phenylcyclopropyl)pip...)
Affinity DataIC50: 7.5nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295539BDBM50295539(4-(benzo[d]oxazol-2-yl)-N-(2-phenylcyclopropyl)pip...)
Affinity DataIC50: 8nMAssay Description:Inhibition of human sEH in HEK293 cells assessed as conversion of 14,15-epoxyeicosatrienoic acid to 14,15-dihydroepoxyeicosatrienoic acidMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295532BDBM50295532(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(1,2,3...)
Affinity DataIC50: 8nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295548BDBM50295548(N-(2-phenylcyclopropyl)-4-(3-(quinolin-2-yl)-1,2,4...)
Affinity DataIC50: 8nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295534BDBM50295534(N-((1R,2S)-2-phenylcyclopropyl)-4-(3-(pyridin-2-yl...)
Affinity DataIC50: 9nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295540BDBM50295540(N-(2-phenylcyclopropyl)-4-(3-(2-(trifluoromethyl)p...)
Affinity DataIC50: 9nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295547BDBM50295547(4-(3-(isoquinolin-1-yl)-1,2,4-oxadiazol-5-yl)-N-(2...)
Affinity DataIC50: 10nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295535BDBM50295535(1-butyl-N-(2,3-dimethoxybenzyl)-2-(3,4,5-trimethox...)
Affinity DataIC50: 10nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295534BDBM50295534(N-((1R,2S)-2-phenylcyclopropyl)-4-(3-(pyridin-2-yl...)
Affinity DataIC50: 10nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295543BDBM50295543(N-(2-phenylcyclopropyl)-4-(3-(pyridin-3-yl)-1,2,4-...)
Affinity DataIC50: 10nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295541BDBM50295541(4-(3-(4-(methylsulfonyl)phenyl)-1,2,4-oxadiazol-5-...)
Affinity DataIC50: 11nMAssay Description:Inhibition of human sEH in HEK293 cells assessed as conversion of 14,15-epoxyeicosatrienoic acid to 14,15-dihydroepoxyeicosatrienoic acidMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295545BDBM50295545(N-(2-phenylcyclopropyl)-4-(3-(pyrazin-2-yl)-1,2,4-...)
Affinity DataIC50: 11nMAssay Description:Inhibition of human sEH in HEK293 cells assessed as conversion of 14,15-epoxyeicosatrienoic acid to 14,15-dihydroepoxyeicosatrienoic acidMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295541BDBM50295541(4-(3-(4-(methylsulfonyl)phenyl)-1,2,4-oxadiazol-5-...)
Affinity DataIC50: 12nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295545BDBM50295545(N-(2-phenylcyclopropyl)-4-(3-(pyrazin-2-yl)-1,2,4-...)
Affinity DataIC50: 13nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295543BDBM50295543(N-(2-phenylcyclopropyl)-4-(3-(pyridin-3-yl)-1,2,4-...)
Affinity DataIC50: 13nMAssay Description:Inhibition of human sEH in HEK293 cells assessed as conversion of 14,15-epoxyeicosatrienoic acid to 14,15-dihydroepoxyeicosatrienoic acidMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295534BDBM50295534(N-((1R,2S)-2-phenylcyclopropyl)-4-(3-(pyridin-2-yl...)
Affinity DataIC50: 14nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295544BDBM50295544(N-(2-phenylcyclopropyl)-4-(3-(pyridin-4-yl)-1,2,4-...)
Affinity DataIC50: 14nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295550BDBM50295550(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(6,7,8...)
Affinity DataIC50: 15nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295544BDBM50295544(N-(2-phenylcyclopropyl)-4-(3-(pyridin-4-yl)-1,2,4-...)
Affinity DataIC50: 15nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295539BDBM50295539(4-(benzo[d]oxazol-2-yl)-N-(2-phenylcyclopropyl)pip...)
Affinity DataIC50: 16nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295545BDBM50295545(N-(2-phenylcyclopropyl)-4-(3-(pyrazin-2-yl)-1,2,4-...)
Affinity DataIC50: 17nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295549BDBM50295549(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(4-(tr...)
Affinity DataIC50: 17nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295542BDBM50295542(4-(5-(1-(2-phenylcyclopropylcarbamoyl)piperidin-4-...)
Affinity DataIC50: 17nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295534BDBM50295534(N-((1R,2S)-2-phenylcyclopropyl)-4-(3-(pyridin-2-yl...)
Affinity DataIC50: 18nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295534BDBM50295534(N-((1R,2S)-2-phenylcyclopropyl)-4-(3-(pyridin-2-yl...)
Affinity DataIC50: 18nMAssay Description:Inhibition of human sEH in HEK293 cells assessed as conversion of 14,15-epoxyeicosatrienoic acid to 14,15-dihydroepoxyeicosatrienoic acidMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295547BDBM50295547(4-(3-(isoquinolin-1-yl)-1,2,4-oxadiazol-5-yl)-N-(2...)
Affinity DataIC50: 21nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295532BDBM50295532(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(1,2,3...)
Affinity DataIC50: 22nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295534BDBM50295534(N-((1R,2S)-2-phenylcyclopropyl)-4-(3-(pyridin-2-yl...)
Affinity DataIC50: 27nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295538BDBM50295538(4-(3-methyl-1,2,4-oxadiazol-5-yl)-N-(2-phenylcyclo...)
Affinity DataIC50: 28nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295544BDBM50295544(N-(2-phenylcyclopropyl)-4-(3-(pyridin-4-yl)-1,2,4-...)
Affinity DataIC50: 30nMAssay Description:Inhibition of human sEH in HEK293 cells assessed as conversion of 14,15-epoxyeicosatrienoic acid to 14,15-dihydroepoxyeicosatrienoic acidMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295546BDBM50295546(N-(2-phenylcyclopropyl)-4-(3-(pyrimidin-2-yl)-1,2,...)
Affinity DataIC50: 33nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295534BDBM50295534(N-((1R,2S)-2-phenylcyclopropyl)-4-(3-(pyridin-2-yl...)
Affinity DataIC50: 34nMAssay Description:Inhibition of human sEH in HEK293 cells assessed as conversion of 14,15-epoxyeicosatrienoic acid to 14,15-dihydroepoxyeicosatrienoic acidMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295547BDBM50295547(4-(3-(isoquinolin-1-yl)-1,2,4-oxadiazol-5-yl)-N-(2...)
Affinity DataIC50: 35nMAssay Description:Inhibition of human sEH in HEK293 cells assessed as conversion of 14,15-epoxyeicosatrienoic acid to 14,15-dihydroepoxyeicosatrienoic acidMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295546BDBM50295546(N-(2-phenylcyclopropyl)-4-(3-(pyrimidin-2-yl)-1,2,...)
Affinity DataIC50: 35nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295550BDBM50295550(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(6,7,8...)
Affinity DataIC50: 36nMAssay Description:Inhibition of human sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295538BDBM50295538(4-(3-methyl-1,2,4-oxadiazol-5-yl)-N-(2-phenylcyclo...)
Affinity DataIC50: 48nMAssay Description:Inhibition of rat sEHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50295532BDBM50295532(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(1,2,3...)
Affinity DataIC50: 49nMAssay Description:Inhibition of human sEH in HEK293 cells assessed as conversion of 14,15-epoxyeicosatrienoic acid to 14,15-dihydroepoxyeicosatrienoic acidMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/24/2012
Entry Details Article
PubMed
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