Compile Data Set for Download or QSAR
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Report error Found 10 Enz. Inhib. hit(s) with all data for entry = 50009522
TargetCannabinoid receptor 2(Human)
Univerisity of Eastern Finland (Uef)

Curated by ChEMBL
LigandPNGBDBM50529607(Beta-Caryophylene | Beta-Caryophyllene | CHEBI:103...)
Affinity DataKi:  150nMAssay Description:Displacement of [3H]CP55940 from human CB2 expressed in CHOK1 cell membranes after 2 hrs by liquid scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetCannabinoid receptor 2(Human)
Univerisity of Eastern Finland (Uef)

Curated by ChEMBL
LigandPNGBDBM50529607(Beta-Caryophylene | Beta-Caryophyllene | CHEBI:103...)
Affinity DataKi:  150nMAssay Description:Displacement of [3H]CP55940 from human CB2 expressed in CHOK1 cell membranes after 2 hrs by liquid scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetNeuronal acetylcholine receptor subunit alpha-7(Human)
Univerisity of Eastern Finland (Uef)

Curated by ChEMBL
LigandPNGBDBM50382730((-)-ALPHA-BISABOLOL | ALPHA-BISABOLOL)
Affinity DataIC50:  3.10E+3nMAssay Description:Antagonist activity at human alpha7 nACHR expressed in Xenopus laevis oocytes assessed as inhibition of acetylcholine-induced currents at -70 mV hold...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetNeuronal acetylcholine receptor subunit alpha-7(Human)
Univerisity of Eastern Finland (Uef)

Curated by ChEMBL
LigandPNGBDBM50382730((-)-ALPHA-BISABOLOL | ALPHA-BISABOLOL)
Affinity DataIC50:  3.10E+3nMAssay Description:Antagonist activity at human alpha7 nACHR expressed in Xenopus laevis oocytes assessed as inhibition of acetylcholine-induced currents at -70 mV hold...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetTransient receptor potential cation channel subfamily A member 1(Human)
Univerisity of Eastern Finland (Uef)

Curated by ChEMBL
LigandPNGBDBM36265((+)-borneol)
Affinity DataIC50:  3.00E+5nMAssay Description:Antagonist activity at TRPA1 (unknown origin) expressed in Xenopus laevis oocytes assessed as inhibition of mustard oil-induced currents by two-elect...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetTransient receptor potential cation channel subfamily A member 1(Human)
Univerisity of Eastern Finland (Uef)

Curated by ChEMBL
LigandPNGBDBM36265((+)-borneol)
Affinity DataIC50:  3.00E+5nMAssay Description:Antagonist activity at TRPA1 (unknown origin) expressed in Xenopus laevis oocytes assessed as inhibition of mustard oil-induced currents by two-elect...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetCannabinoid receptor 2(Human)
Univerisity of Eastern Finland (Uef)

Curated by ChEMBL
LigandPNGBDBM50529607(Beta-Caryophylene | Beta-Caryophyllene | CHEBI:103...)
Affinity DataEC50:  1.90E+3nMAssay Description:Agonist activity at recombinant human Cb2 receptor expressed in CHOK1 cells assessed as inhibition of forskolin-stimulated cAMP levels measured up to...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetTransient receptor potential cation channel subfamily A member 1(Human)
Univerisity of Eastern Finland (Uef)

Curated by ChEMBL
LigandPNGBDBM50529606(Beta-Eudesmol | CHEBI:10417)
Affinity DataEC50:  3.30E+4nMAssay Description:Agonist activity at human TRPA1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetCannabinoid receptor 2(Human)
Univerisity of Eastern Finland (Uef)

Curated by ChEMBL
LigandPNGBDBM50529607(Beta-Caryophylene | Beta-Caryophyllene | CHEBI:103...)
Affinity DataEC50:  1.90E+3nMAssay Description:Agonist activity at recombinant human Cb2 receptor expressed in CHOK1 cells assessed as inhibition of forskolin-stimulated cAMP levels measured up to...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetTransient receptor potential cation channel subfamily A member 1(Human)
Univerisity of Eastern Finland (Uef)

Curated by ChEMBL
LigandPNGBDBM50529606(Beta-Eudesmol | CHEBI:10417)
Affinity DataEC50:  3.30E+4nMAssay Description:Agonist activity at human TRPA1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed