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Found 118 with Last Name = 'schiano-moriello' and Initial = 'a'
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM20461((6E)-N-[(4-hydroxy-3-methoxyphenyl)methyl]-8-methy...)
Affinity DataIC50:  8nMAssay Description:Antagonist activity against human recombinant TRPV1 expressed in HEK293 cells assessed as inhibition of capsaicin-induced Ca2+ influx pre-treated 5 m...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
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))
Universit£

Curated by ChEMBL
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))
Universit£

Curated by ChEMBL
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 A member 1(Rattus norvegicus)
University Of Naples Federico Ii

Curated by ChEMBL
LigandPNGBDBM50318484(2-((1R,6R)-6-Isopropenyl-3-methyl-cyclohex-2-enyl)...)
Affinity DataIC50:  450nMAssay Description:Antagonist activity at rat TRPA1 expressed in HEK293 cells assessed as inhibition of allylisothiocyanate-induced Ca2+ response preincubated for 5 min...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
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))
Universit£

Curated by ChEMBL
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))
Universit£

Curated by ChEMBL
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))
Universit£

Curated by ChEMBL
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
TargetHeat sensitive channel TRPV3(Rattus norvegicus)
University Of Naples Federico Ii

Curated by ChEMBL
LigandPNGBDBM50318484(2-((1R,6R)-6-Isopropenyl-3-methyl-cyclohex-2-enyl)...)
Affinity DataIC50:  750nMAssay Description:Antagonist activity at rat TRPV3 expressed in HEK293 cells assessed as inhibition of thymol-induced Ca2+ response preincubated for 5 mins followed by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
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))
Universit£

Curated by ChEMBL
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
TargetTransient receptor potential cation channel subfamily A member 1(Rattus norvegicus)
University Of Naples Federico Ii

Curated by ChEMBL
LigandPNGBDBM50103439(CHEMBL3398239)
Affinity DataIC50:  1.00E+3nMAssay Description:Antagonist activity against rat recombinant TRPA1 expressed in HEK293 cells assessed as inhibition of AITC-induced Ca2+ influx pre-treated 5 mins bef...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 2(Rattus norvegicus)
University Of Naples Federico Ii

Curated by ChEMBL
LigandPNGBDBM50318484(2-((1R,6R)-6-Isopropenyl-3-methyl-cyclohex-2-enyl)...)
Affinity DataIC50:  1.10E+3nMAssay Description:Antagonist activity at rat TRPV2 expressed in HEK293 cells assessed as inhibition of LPC-induced Ca2+ response preincubated for 5 mins followed by LP...More data for this Ligand-Target Pair
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
TargetTransient receptor potential cation channel subfamily A member 1(Rattus norvegicus)
University Of Naples Federico Ii

Curated by ChEMBL
LigandPNGBDBM50103440(CHEMBL3398238)
Affinity DataIC50:  1.71E+3nMAssay Description:Antagonist activity against rat recombinant TRPA1 expressed in HEK293 cells assessed as inhibition of AITC-induced Ca2+ influx pre-treated 5 mins bef...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))
Universit£

Curated by ChEMBL
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))
Universit£

Curated by ChEMBL
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))
Universit£

Curated by ChEMBL
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))
Universit£

Curated by ChEMBL
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))
Universit£

Curated by ChEMBL
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 M member 8(Rattus norvegicus (Rat))
University Of Naples Federico Ii

Curated by ChEMBL
LigandPNGBDBM50318484(2-((1R,6R)-6-Isopropenyl-3-methyl-cyclohex-2-enyl)...)
Affinity DataIC50:  2.80E+3nMAssay Description:Antagonist activity at rat TRPM8 expressed in HEK293 cells assessed as inhibition of icilin-induced Ca2+ response preincubated for 5 mins followed by...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
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
TargetTransient receptor potential cation channel subfamily A member 1(Rattus norvegicus)
University Of Naples Federico Ii

Curated by ChEMBL
LigandPNGBDBM50103441(CHEMBL3398241)
Affinity DataIC50:  2.90E+3nMAssay Description:Antagonist activity against rat recombinant TRPA1 expressed in HEK293 cells assessed as inhibition of AITC-induced Ca2+ influx pre-treated 5 mins bef...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
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50318484(2-((1R,6R)-6-Isopropenyl-3-methyl-cyclohex-2-enyl)...)
Affinity DataIC50:  3.70E+3nMAssay Description:Antagonist activity at human TRPV1 expressed in HEK293 cells assessed as inhibition of capsaicin-induced Ca2+ response preincubated for 5 mins follow...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))
Universit£

Curated by ChEMBL
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
TargetTransient receptor potential cation channel subfamily M member 8(Rattus norvegicus (Rat))
University Of Naples Federico Ii

Curated by ChEMBL
LigandPNGBDBM50548384(CHEMBL4762439)
Affinity DataIC50:  3.90E+3nMAssay Description:Antagonist activity at rat TRPM8 expressed in HEK293 cells assessed as inhibition of icilin-induced Ca2+ response preincubated for 5 mins followed by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily A member 1(Rattus norvegicus)
University Of Naples Federico Ii

Curated by ChEMBL
LigandPNGBDBM50548384(CHEMBL4762439)
Affinity DataIC50:  4.90E+3nMAssay Description:Antagonist activity at rat TRPA1 expressed in HEK293 cells assessed as inhibition of allylisothiocyanate-induced Ca2+ response preincubated for 5 min...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
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))
Universit£

Curated by ChEMBL
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
TargetTransient receptor potential cation channel subfamily V member 4(Rattus norvegicus)
University Of Naples Federico Ii

Curated by ChEMBL
LigandPNGBDBM50318484(2-((1R,6R)-6-Isopropenyl-3-methyl-cyclohex-2-enyl)...)
Affinity DataIC50:  5.90E+3nMAssay Description:Antagonist activity at rat TRPV4 expressed in HEK293 cells assessed as inhibition of GSK1016790A-induced Ca2+ response preincubated for 5 mins follow...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))
Universit£

Curated by ChEMBL
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
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))
Universit£

Curated by ChEMBL
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
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
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))
Universit£

Curated by ChEMBL
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))
Universit£

Curated by ChEMBL
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))
Universit£

Curated by ChEMBL
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))
Universit£

Curated by ChEMBL
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))
Universit£

Curated by ChEMBL
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
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