Compile Data Set for Download or QSAR
maximum 50k data
Found 59 Enz. Inhib. hit(s) with all data for entry = 50010299
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50019355(1-(3,4,5-Trimethoxy-benzyl)-1,2,3,4-tetrahydro-iso...)
Affinity DataIC50:  6.10nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human beta2 adrenergic receptor (AR) in the presence of [1...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50019355(1-(3,4,5-Trimethoxy-benzyl)-1,2,3,4-tetrahydro-iso...)
Affinity DataIC50:  6.10nMAssay Description:Compound was evaluated for its inhibitory activity against human beta1 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093039(4-(3,5-Diiodo-4-methoxy-benzyl)-4,5,6,7-tetrahydro...)
Affinity DataIC50:  56nMAssay Description:Percent adenylyl cyclase activation at 10000 nM of compound concentrationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093037(CHEMBL312074 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataIC50:  160nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human beta2 adrenergic receptor (AR) in the presence of [1...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093040(CHEMBL74085 | N-[4-(6,7-Dihydroxy-1,2,3,4-tetrahyd...)
Affinity DataIC50:  200nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human Beta-1 adrenergic receptor in the presence of [125I]...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093041(CHEMBL67998 | N-[6-(6,7-Dihydroxy-1,2,3,4-tetrahyd...)
Affinity DataIC50:  300nMAssay Description:Inhibitory activity against CHO cells expressing human Beta-2 adrenergic receptor with [125I]-iodocyanopindololMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093035(CHEMBL308126 | N-[4-(6,7-Dihydroxy-1,2,3,4-tetrahy...)
Affinity DataIC50:  300nMAssay Description:Inhibitory activity against CHO cells expressing human Beta-2 adrenergic receptor with [125I]-iodocyanopindololMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093033(CHEMBL308868 | N-[3'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataIC50:  530nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human beta1 adrenergic receptor (AR) in the presence of [1...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093033(CHEMBL308868 | N-[3'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataIC50:  710nMAssay Description:Inhibitory activity against CHO cells expressing human Beta-2 adrenergic receptor with [125I]-iodocyanopindololMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093038(1-(3',4',5'-Trimethoxy-biphenyl-4-ylmethyl)-1,2,3,...)
Affinity DataIC50:  760nMAssay Description:Compound was evaluated for its inhibitory activity against human beta1 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093039(4-(3,5-Diiodo-4-methoxy-benzyl)-4,5,6,7-tetrahydro...)
Affinity DataIC50:  780nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human Beta-1 adrenergic receptor in the presence of [125I]...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093043(CHEMBL308860 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataIC50:  990nMAssay Description:Inhibitory activity against CHO cells expressing human Beta-2 adrenergic receptor with [125I]-iodocyanopindololMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093041(CHEMBL67998 | N-[6-(6,7-Dihydroxy-1,2,3,4-tetrahyd...)
Affinity DataIC50:  1.00E+3nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human Beta-1 adrenergic receptor in the presence of [125I]...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093035(CHEMBL308126 | N-[4-(6,7-Dihydroxy-1,2,3,4-tetrahy...)
Affinity DataIC50:  1.00E+3nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human Beta-1 adrenergic receptor in the presence of [125I]...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093040(CHEMBL74085 | N-[4-(6,7-Dihydroxy-1,2,3,4-tetrahyd...)
Affinity DataIC50:  1.20E+3nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human Beta-1 adrenergic receptor in the presence of [125I]...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093038(1-(3',4',5'-Trimethoxy-biphenyl-4-ylmethyl)-1,2,3,...)
Affinity DataIC50:  1.80E+3nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human beta1 adrenergic receptor (AR) in the presence of [1...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093037(CHEMBL312074 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataIC50:  2.00E+3nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human Beta-1 adrenergic receptor in the presence of [125I]...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093044(CHEMBL75604 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrahy...)
Affinity DataIC50:  3.00E+3nMAssay Description:Percent adenylyl cyclase activation at 10000 nM of compound concentrationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093044(CHEMBL75604 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrahy...)
Affinity DataIC50:  3.40E+3nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human beta2 adrenergic receptor (AR) in the presence of [1...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093043(CHEMBL308860 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataIC50:  6.50E+3nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human Beta-1 adrenergic receptor in the presence of [125I]...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093034(CHEMBL305891 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataIC50:  1.00E+4nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human beta1 adrenergic receptor (AR) in the presence of [1...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093034(CHEMBL305891 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataIC50:  3.20E+4nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human beta2 adrenergic receptor (AR) in the presence of [1...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093036(CHEMBL76403 | N-[6-(6,7-Dihydroxy-1,2,3,4-tetrahyd...)
Affinity DataIC50:  8.00E+4nMAssay Description:Compound was evaluated for its inhibitory activity against human beta2 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093036(CHEMBL76403 | N-[6-(6,7-Dihydroxy-1,2,3,4-tetrahyd...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibitory activity against CHO cells expressing human Beta-2 adrenergic receptor with [125I]-iodocyanopindololMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093042(CHEMBL74860 | N-[3'-(6,7-Dihydroxy-1,2,3,4-tetrahy...)
Affinity DataIC50:  1.00E+5nMAssay Description:Compound was evaluated for its inhibitory activity against human beta2 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093042(CHEMBL74860 | N-[3'-(6,7-Dihydroxy-1,2,3,4-tetrahy...)
Affinity DataIC50:  1.00E+5nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human beta1 adrenergic receptor (AR) in the presence of [1...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093040(CHEMBL74085 | N-[4-(6,7-Dihydroxy-1,2,3,4-tetrahyd...)
Affinity DataEC50:  19nMAssay Description:Compound was evaluated for its inhibitory activity against human beta2 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093037(CHEMBL312074 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataEC50:  580nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human beta1 adrenergic receptor (AR) in the presence of [1...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093033(CHEMBL308868 | N-[3'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataEC50:  2.70E+3nMAssay Description:Compound was evaluated for its inhibitory activity against human beta2 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093044(CHEMBL75604 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrahy...)
Affinity DataEC50:  340nMAssay Description:Inhibitory activity against CHO cells expressing human Beta-2 adrenergic receptor with [125I]-iodocyanopindololMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093036(CHEMBL76403 | N-[6-(6,7-Dihydroxy-1,2,3,4-tetrahyd...)
Affinity DataEC50:  37nMAssay Description:Compound was evaluated for its inhibitory activity against CHO cells expressing the cloned human beta1 adrenergic receptor (AR) in the presence of [1...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093033(CHEMBL308868 | N-[3'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataEC50:  1.00E+4nMAssay Description:Percent adenylyl cyclase activation at 10000 nM of compound concentrationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093038(1-(3',4',5'-Trimethoxy-biphenyl-4-ylmethyl)-1,2,3,...)
Affinity DataEC50:  6.10E+3nMAssay Description:Inhibitory activity against CHO cells expressing human Beta-2 adrenergic receptor with [125I]-iodocyanopindololMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093039(4-(3,5-Diiodo-4-methoxy-benzyl)-4,5,6,7-tetrahydro...)
Affinity DataEC50:  2nMAssay Description:Inhibitory activity against CHO cells expressing human Beta-2 adrenergic receptor with [125I]-iodocyanopindololMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093034(CHEMBL305891 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataEC50:  1.30E+3nMAssay Description:Inhibitory activity against CHO cells expressing human Beta-2 adrenergic receptor with [125I]-iodocyanopindololMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-3 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093043(CHEMBL308860 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataEC50:  10nMAssay Description:Compound was evaluated for its inhibitory activity against human beta3 adrenergic receptor (AR) at a concentration of 100 nMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-3 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093044(CHEMBL75604 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrahy...)
Affinity DataEC50:  6nMAssay Description:Inhibitory activity against human beta3 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093044(CHEMBL75604 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrahy...)
Affinity DataEC50:  1.80E+3nMAssay Description:Compound was evaluated for its inhibitory activity against human beta1 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-3 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093040(CHEMBL74085 | N-[4-(6,7-Dihydroxy-1,2,3,4-tetrahyd...)
Affinity DataEC50:  66nMAssay Description:Inhibitory activity against human beta3 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-3 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093037(CHEMBL312074 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataEC50:  16nMAssay Description:Inhibitory activity against human beta3 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-3 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50019355(1-(3,4,5-Trimethoxy-benzyl)-1,2,3,4-tetrahydro-iso...)
Affinity DataEC50:  1.70nMAssay Description:Inhibitory activity against human beta3 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-3 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093034(CHEMBL305891 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataEC50:  140nMAssay Description:Inhibitory activity against human beta3 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093042(CHEMBL74860 | N-[3'-(6,7-Dihydroxy-1,2,3,4-tetrahy...)
Affinity DataEC50: >1.00E+3nMAssay Description:Compound was evaluated for its inhibitory activity against human beta1 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-3 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093036(CHEMBL76403 | N-[6-(6,7-Dihydroxy-1,2,3,4-tetrahyd...)
Affinity DataEC50:  78nMAssay Description:Inhibitory activity against human beta3 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-3 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093042(CHEMBL74860 | N-[3'-(6,7-Dihydroxy-1,2,3,4-tetrahy...)
Affinity DataEC50:  600nMAssay Description:Inhibitory activity against human beta3 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-3 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093041(CHEMBL67998 | N-[6-(6,7-Dihydroxy-1,2,3,4-tetrahyd...)
Affinity DataEC50:  7nMAssay Description:Compound was evaluated for its inhibitory activity against human beta3 adrenergic receptor (AR) at a concentration of 100 nMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-3 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093038(1-(3',4',5'-Trimethoxy-biphenyl-4-ylmethyl)-1,2,3,...)
Affinity DataEC50:  27nMAssay Description:Inhibitory activity against human beta3 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50019355(1-(3,4,5-Trimethoxy-benzyl)-1,2,3,4-tetrahydro-iso...)
Affinity DataEC50:  14nMAssay Description:Compound was evaluated for its inhibitory activity against human Beta-1 adrenergic receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093034(CHEMBL305891 | N-[4'-(6,7-Dihydroxy-1,2,3,4-tetrah...)
Affinity DataEC50:  970nMAssay Description:Compound was evaluated for its inhibitory activity against human beta1 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-3 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50093039(4-(3,5-Diiodo-4-methoxy-benzyl)-4,5,6,7-tetrahydro...)
Affinity DataEC50:  800nMAssay Description:Inhibitory activity against human beta3 adrenergic receptor (AR)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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