Compile Data Set for Download or QSAR
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Found 18 Enz. Inhib. hit(s) with all data for entry = 50036028
TargetMu-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001092(13-[2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-prop...)
Affinity DataKi:  0.900nMAssay Description:Compound was evaluated for its binding affinity by displacement of [3H]- DAMPGO from opioid receptor mu by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001092(13-[2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-prop...)
Affinity DataKi:  0.900nMAssay Description:Compound was evaluated for its binding affinity by displacement [3H]- DSLET from Opioid receptor delta 1 by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001090(13-[2-Amino-3-(4-hydroxy-phenyl)-propionylamino]-7...)
Affinity DataKi:  2.5nMAssay Description:Compound was evaluated for its binding affinity by displacement [3H]- DSLET from Opioid receptor delta 1 by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001088((DPDPE)13-[2-Amino-3-(4-hydroxy-phenyl)-propionyla...)
Affinity DataKi:  7nMAssay Description:Compound was evaluated for its binding affinity by displacement [3H]- DSLET from Opioid receptor delta 1 by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001090(13-[2-Amino-3-(4-hydroxy-phenyl)-propionylamino]-7...)
Affinity DataKi:  9.5nMAssay Description:Compound was evaluated for its binding affinity by displacement of [3H]- DAMPGO from opioid receptor mu by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001093(13-[2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-prop...)
Affinity DataKi:  11nMAssay Description:Compound was evaluated for its binding affinity by displacement [3H]- DSLET from Opioid receptor delta 1 by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001093(13-[2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-prop...)
Affinity DataKi:  11nMAssay Description:Compound was evaluated for its binding affinity by displacement of [3H]- DAMPGO from opioid receptor mu by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001093(13-[2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-prop...)
Affinity DataKi:  21nMAssay Description:Compound was evaluated for its binding affinity by displacement [3H]- DSLET from Opioid receptor delta 1 by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001093(13-[2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-prop...)
Affinity DataKi:  21nMAssay Description:Compound was evaluated for its binding affinity by displacement [3H]- DSLET from Opioid receptor delta 1 by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001089(13-[2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-prop...)
Affinity DataKi:  32nMAssay Description:Compound was evaluated for its binding affinity by displacement of [3H]- DAMPGO from opioid receptor mu by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001089(13-[2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-prop...)
Affinity DataKi:  32nMAssay Description:Dissociation rate constant of compound for mutant T46S Escherichia coli dihydrofolate reductaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001089(13-[2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-prop...)
Affinity DataKi:  45nMAssay Description:Compound was evaluated for its binding affinity by displacement [3H]- DSLET from Opioid receptor delta 1 by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001089(13-[2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-prop...)
Affinity DataKi:  45nMAssay Description:Compound was evaluated for its binding affinity by displacement [3H]- DSLET from Opioid receptor delta 1 by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001091(10-[2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-prop...)
Affinity DataKi:  91nMAssay Description:Compound was evaluated for its binding affinity by displacement [3H]- DSLET from Opioid receptor delta 1 by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001091(10-[2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-prop...)
Affinity DataKi:  91nMAssay Description:Dissociation rate constant of compound for mutant T46A Escherichia coli dihydrofolate reductaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001091(10-[2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-prop...)
Affinity DataKi:  150nMAssay Description:Compound was evaluated for its binding affinity by displacement of [3H]- DAMPGO from opioid receptor mu by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001091(10-[2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-prop...)
Affinity DataKi:  150nMAssay Description:Compound was evaluated for its binding affinity by displacement of [3H]- DAMPGO from opioid receptor mu by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
G.D. Searle And

Curated by ChEMBL
LigandPNGBDBM50001088((DPDPE)13-[2-Amino-3-(4-hydroxy-phenyl)-propionyla...)
Affinity DataKi:  700nMAssay Description:Compound was evaluated for its binding affinity by displacement of [3H]- DAMPGO from opioid receptor mu by using opioid radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed