Compile Data Set for Download or QSAR
maximum 50k data
Found 78 Enz. Inhib. hit(s) with all data for entry = 2657
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM22999(N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-2-(3-pentylph...)
Affinity DataIC50:  240nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM22987((5Z,8Z,11Z,14Z)-N-[2-(5-hydroxy-1H-indol-3-yl)ethy...)
Affinity DataIC50:  270nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23000(JMC506554 Compound 1m | N-[2-(5-hydroxy-1H-indol-3...)
Affinity DataIC50:  430nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM22989((9Z,12Z,15Z)-N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]o...)
Affinity DataIC50:  470nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Sapienza University of Rome

LigandPNGBDBM23015(3-phenylphenyl N-[2-(5-hydroxy-1H-indol-3-yl)ethyl...)
Affinity DataIC50:  500nMpH: 9.0 T: 2°CAssay Description:The effect of the test compounds on the enzymatic hydrolysis of [14C]anandamide was evaluated by using membranes prepared from rat brain. [14C]Ethano...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM22998(N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-9-phenylnonan...)
Affinity DataIC50:  680nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23007(3-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-1-(3-phenylph...)
Affinity DataIC50:  720nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM22995(N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]dodecanamide |...)
Affinity DataIC50:  740nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM22994(N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]undecanamide |...)
Affinity DataIC50:  760nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM22990((6Z,9Z,12Z)-N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]oc...)
Affinity DataIC50:  950nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Sapienza University of Rome

LigandPNGBDBM23026(4-(benzyloxy)phenyl N-[2-(5-hydroxy-1H-indol-3-yl)...)
Affinity DataIC50:  1.17E+3nMAssay Description:The effect of the test compounds on the enzymatic hydrolysis of [14C]anandamide was evaluated by using membranes prepared from rat brain. [14C]Ethano...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Sapienza University of Rome

LigandPNGBDBM23022(3-iodophenyl N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]c...)
Affinity DataIC50:  1.80E+3nMAssay Description:The effect of the test compounds on the enzymatic hydrolysis of [14C]anandamide was evaluated by using membranes prepared from rat brain. [14C]Ethano...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM22991((9Z,12Z)-N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]octad...)
Affinity DataIC50:  1.82E+3nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Sapienza University of Rome

LigandPNGBDBM23020(3-chlorophenyl N-[2-(5-hydroxy-1H-indol-3-yl)ethyl...)
Affinity DataIC50:  1.90E+3nMAssay Description:The effect of the test compounds on the enzymatic hydrolysis of [14C]anandamide was evaluated by using membranes prepared from rat brain. [14C]Ethano...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM22997(N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-8-phenyloctan...)
Affinity DataIC50:  2.13E+3nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Sapienza University of Rome

LigandPNGBDBM23018(3-(trifluoromethyl)phenyl N-[2-(5-hydroxy-1H-indol...)
Affinity DataIC50:  2.20E+3nMAssay Description:The effect of the test compounds on the enzymatic hydrolysis of [14C]anandamide was evaluated by using membranes prepared from rat brain. [14C]Ethano...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23014(3-pentylphenyl N-[2-(5-hydroxy-1H-indol-3-yl)ethyl...)
Affinity DataIC50:  2.40E+3nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM22992((9Z)-N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]octadec-9...)
Affinity DataIC50:  2.57E+3nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23004(3-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-1-(3-pentylph...)
Affinity DataIC50:  2.63E+3nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23010((5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraen-1-yl N-[2-...)
Affinity DataIC50:  2.82E+3nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Sapienza University of Rome

LigandPNGBDBM23014(3-pentylphenyl N-[2-(5-hydroxy-1H-indol-3-yl)ethyl...)
Affinity DataIC50:  3.60E+3nMpH: 9.0 T: 2°CAssay Description:The effect of the test compounds on the enzymatic hydrolysis of [14C]anandamide was evaluated by using membranes prepared from rat brain. [14C]Ethano...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Sapienza University of Rome

LigandPNGBDBM23016(3-tert-butylphenyl N-[2-(5-hydroxy-1H-indol-3-yl)e...)
Affinity DataIC50:  3.70E+3nMpH: 9.0 T: 2°CAssay Description:The effect of the test compounds on the enzymatic hydrolysis of [14C]anandamide was evaluated by using membranes prepared from rat brain. [14C]Ethano...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23003(1-[(4-tert-butylphenyl)methyl]-3-[2-(5-hydroxy-1H-...)
Affinity DataIC50:  3.80E+3nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Sapienza University of Rome

LigandPNGBDBM23023(4-iodophenyl N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]c...)
Affinity DataIC50:  5.00E+3nMAssay Description:The effect of the test compounds on the enzymatic hydrolysis of [14C]anandamide was evaluated by using membranes prepared from rat brain. [14C]Ethano...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23017(4-tert-butylphenyl N-[2-(5-hydroxy-1H-indol-3-yl)e...)
Affinity DataIC50:  5.25E+3nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Sapienza University of Rome

LigandPNGBDBM23019(4-(trifluoromethyl)phenyl N-[2-(5-hydroxy-1H-indol...)
Affinity DataIC50:  6.40E+3nMAssay Description:The effect of the test compounds on the enzymatic hydrolysis of [14C]anandamide was evaluated by using membranes prepared from rat brain. [14C]Ethano...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Sapienza University of Rome

LigandPNGBDBM23021(4-chlorophenyl N-[2-(5-hydroxy-1H-indol-3-yl)ethyl...)
Affinity DataIC50:  6.80E+3nMAssay Description:The effect of the test compounds on the enzymatic hydrolysis of [14C]anandamide was evaluated by using membranes prepared from rat brain. [14C]Ethano...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Sapienza University of Rome

LigandPNGBDBM22987((5Z,8Z,11Z,14Z)-N-[2-(5-hydroxy-1H-indol-3-yl)ethy...)
Affinity DataIC50:  8.00E+3nMpH: 9.0 T: 2°CAssay Description:The effect of the test compounds on the enzymatic hydrolysis of [14C]anandamide was evaluated by using membranes prepared from rat brain. [14C]Ethano...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM22996(N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-7-phenylhepta...)
Affinity DataIC50:  9.12E+3nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23026(4-(benzyloxy)phenyl N-[2-(5-hydroxy-1H-indol-3-yl)...)
Affinity DataIC50: >1.00E+4nMT: 2°CAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Sapienza University of Rome

LigandPNGBDBM22989((9Z,12Z,15Z)-N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]o...)
Affinity DataIC50:  1.00E+4nMpH: 9.0 T: 2°CAssay Description:The effect of the test compounds on the enzymatic hydrolysis of [14C]anandamide was evaluated by using membranes prepared from rat brain. [14C]Ethano...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Sapienza University of Rome

LigandPNGBDBM22990((6Z,9Z,12Z)-N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]oc...)
Affinity DataIC50:  1.00E+4nMpH: 9.0 T: 2°CAssay Description:The effect of the test compounds on the enzymatic hydrolysis of [14C]anandamide was evaluated by using membranes prepared from rat brain. [14C]Ethano...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23025(4-methoxyphenyl N-[2-(5-hydroxy-1H-indol-3-yl)ethy...)
Affinity DataIC50: >1.00E+4nMT: 2°CAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23024(N-arachidonoylserotonin carbamate analogue, 3o | n...)
Affinity DataIC50: >1.00E+4nMT: 2°CAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23023(4-iodophenyl N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]c...)
Affinity DataIC50: >1.00E+4nMT: 2°CAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23022(3-iodophenyl N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]c...)
Affinity DataIC50: >1.00E+4nMT: 2°CAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23021(4-chlorophenyl N-[2-(5-hydroxy-1H-indol-3-yl)ethyl...)
Affinity DataIC50: >1.00E+4nMT: 2°CAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23020(3-chlorophenyl N-[2-(5-hydroxy-1H-indol-3-yl)ethyl...)
Affinity DataIC50: >1.00E+4nMT: 2°CAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23019(4-(trifluoromethyl)phenyl N-[2-(5-hydroxy-1H-indol...)
Affinity DataIC50: >1.00E+4nMT: 2°CAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23018(3-(trifluoromethyl)phenyl N-[2-(5-hydroxy-1H-indol...)
Affinity DataIC50: >1.00E+4nMT: 2°CAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Sapienza University of Rome

LigandPNGBDBM23025(4-methoxyphenyl N-[2-(5-hydroxy-1H-indol-3-yl)ethy...)
Affinity DataIC50:  1.00E+4nMAssay Description:The effect of the test compounds on the enzymatic hydrolysis of [14C]anandamide was evaluated by using membranes prepared from rat brain. [14C]Ethano...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Sapienza University of Rome

LigandPNGBDBM23024(N-arachidonoylserotonin carbamate analogue, 3o | n...)
Affinity DataIC50:  1.00E+4nMAssay Description:The effect of the test compounds on the enzymatic hydrolysis of [14C]anandamide was evaluated by using membranes prepared from rat brain. [14C]Ethano...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23016(3-tert-butylphenyl N-[2-(5-hydroxy-1H-indol-3-yl)e...)
Affinity DataIC50: >1.00E+4nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23015(3-phenylphenyl N-[2-(5-hydroxy-1H-indol-3-yl)ethyl...)
Affinity DataIC50: >1.00E+4nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23013((9Z,12Z)-octadeca-9,12-dien-1-yl N-[2-(5-hydroxy-1...)
Affinity DataIC50: >1.00E+4nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23012((6Z,9Z,12Z)-octadeca-6,9,12-trien-1-yl N-[2-(5-hyd...)
Affinity DataIC50: >1.00E+4nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23011((9Z,12Z,15Z)-octadeca-9,12,15-trien-1-yl N-[2-(5-h...)
Affinity DataIC50: >1.00E+4nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23009(3-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-1-[2-(4-pheno...)
Affinity DataIC50: >1.00E+4nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23008(3-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-1-[2-(4-pheny...)
Affinity DataIC50: >1.00E+4nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Sapienza University of Rome

LigandPNGBDBM23006(1-[2-(4-chlorophenyl)ethyl]-3-[2-(5-hydroxy-1H-ind...)
Affinity DataIC50: >1.00E+4nMAssay Description:The antagonistic effects of test compounds were evaluated using HEK293 cells stably overexpressing human TRPV1. Experiments were carried out by measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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