Affinity DataKi: 6nMAssay Description:Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assayMore data for this Ligand-Target Pair
Affinity DataKi: 11nMAssay Description:Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assayMore data for this Ligand-Target Pair
Affinity DataKi: 32nMAssay Description:Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assayMore data for this Ligand-Target Pair
Affinity DataKi: 52nMAssay Description:Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assayMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataKi: 110nMAssay Description:Noncompetitive inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by Dixon plot analysisMore data for this Ligand-Target Pair
Affinity DataKi: 247nMAssay Description:Displacement of [3H]PGD2 from human CRTH2 receptor expressed in CHO cell membrane after 120 mins by scintillation countingMore data for this Ligand-Target Pair
Affinity DataKi: 333nMAssay Description:Displacement of [3H]PGD2 from human CRTH2 receptor expressed in CHO cell membrane after 120 mins by scintillation countingMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataKi: 390nMAssay Description:Competitive inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by Dixon plot analysisMore data for this Ligand-Target Pair
Affinity DataKi: 492nMAssay Description:Displacement of [3H]PGD2 from human CRTH2 receptor expressed in CHO cell membrane after 120 mins by scintillation countingMore data for this Ligand-Target Pair
Affinity DataKi: 520nMAssay Description:Displacement of [3H]PGD2 from human CRTH2 receptor expressed in CHO cell membrane after 120 mins by scintillation countingMore data for this Ligand-Target Pair
Affinity DataKi: 563nMAssay Description:Displacement of [3H]PGD2 from human CRTH2 receptor expressed in CHO cell membrane after 120 mins by scintillation countingMore data for this Ligand-Target Pair
Affinity DataKi: 574nMAssay Description:Displacement of [3H]PGD2 from human CRTH2 receptor expressed in CHO cell membrane after 120 mins by scintillation countingMore data for this Ligand-Target Pair
Affinity DataKi: 591nMAssay Description:Displacement of [3H]PGD2 from human CRTH2 receptor expressed in CHO cell membrane after 120 mins by scintillation countingMore data for this Ligand-Target Pair
Affinity DataKi: 623nMAssay Description:Displacement of [3H]PGD2 from human CRTH2 receptor expressed in CHO cell membrane after 120 mins by scintillation countingMore data for this Ligand-Target Pair
Affinity DataKi: 631nMAssay Description:Displacement of [3H]PGD2 from human CRTH2 receptor expressed in CHO cell membrane after 120 mins by scintillation countingMore data for this Ligand-Target Pair
Affinity DataKi: 752nMAssay Description:Displacement of [3H]PGD2 from human CRTH2 receptor expressed in CHO cell membrane after 120 mins by scintillation countingMore data for this Ligand-Target Pair
Affinity DataKi: 3.00E+3nMAssay Description:Mixed-type inhibition of B6CBAF1/J mouse brain FAAH using [3H]AEA as substrate after 10 mins by Dixon plot analysisMore data for this Ligand-Target Pair
Affinity DataKi: 6.30E+3nMAssay Description:Mixed-type inhibition of B6CBAF1/J mouse brain FAAH using [3H]AEA as substrate after 10 mins by Dixon plot analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Antagonist activity at progesterone receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Antagonist activity at progesterone receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 15nMAssay Description:Inhibition of human carbonic anhydrase 2 using p-nitrophenyl acetate as substrate by UV-VIS spectrophotometric analysisMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 18nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate preincubated for 10 mins at pH 8More data for this Ligand-Target Pair
Affinity DataIC50: 24nMAssay Description:Inhibition of human carbonic anhydrase 9 using p-nitrophenyl acetate as substrate by UV-VIS spectrophotometric analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 31nMAssay Description:Inhibition of human carbonic anhydrase 9 using p-nitrophenyl acetate as substrate by UV-VIS spectrophotometric analysisMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 58nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by liquid scintillation counting analysisMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 58nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by liquid scintillation counting analysisMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 64nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate preincubated for 10 mins at pH 6More data for this Ligand-Target Pair
TargetCarbonic anhydrase 5A, mitochondrial(Homo sapiens (Human))
Jamia Millia Islamia
Curated by ChEMBL
Jamia Millia Islamia
Curated by ChEMBL
Affinity DataIC50: 69nMAssay Description:Inhibition of human carbonic anhydrase 5A using p-nitrophenyl acetate as substrate by UV-VIS spectrophotometric analysisMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 100nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by liquid scintillation counting analysisMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 102nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by liquid scintillation counting analysisMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 130nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by liquid scintillation counting analysisMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 135nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by liquid scintillation counting analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 307nMAssay Description:Antagonist activity at progesterone receptorMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 330nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by liquid scintillation counting analysisMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 331nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by liquid scintillation counting analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 430nMAssay Description:Antagonist activity at progesterone receptorMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 589nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by liquid scintillation counting analysisMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 590nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by liquid scintillation counting analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 650nMAssay Description:Inhibition of FAAH (unknown origin) expressed in human HeLa cells transfected with empty vector using [3H]AEA as substrate after 2 hrs by liquid scin...More data for this Ligand-Target Pair
Affinity DataIC50: 700nMAssay Description:Inhibition of FAAH (unknown origin) expressed in human HeLa cells using [3H]AEA as substrate after 2 hrs by liquid scintillation counting analysisMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 740nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by liquid scintillation counting analysisMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 741nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by liquid scintillation counting analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 771nMAssay Description:Antagonist activity at progesterone receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 771nMAssay Description:Inhibition of human carbonic anhydrase 9 using p-nitrophenyl acetate as substrate by UV-VIS spectrophotometric analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 920nMAssay Description:Inhibition of human carbonic anhydrase 9 using p-nitrophenyl acetate as substrate by UV-VIS spectrophotometric analysisMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 990nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by liquid scintillation counting analysisMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrate after 10 mins by liquid scintillation counting analysisMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 5A, mitochondrial(Homo sapiens (Human))
Jamia Millia Islamia
Curated by ChEMBL
Jamia Millia Islamia
Curated by ChEMBL
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of human carbonic anhydrase 5A using p-nitrophenyl acetate as substrate by UV-VIS spectrophotometric analysisMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
University Of Cagliari
Curated by ChEMBL
University Of Cagliari
Curated by ChEMBL
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of rat brain FAAH using [3H]AEA as substrateMore data for this Ligand-Target Pair
Affinity DataIC50: 1.37E+3nMAssay Description:Inhibition of human carbonic anhydrase 9 using p-nitrophenyl acetate as substrate by UV-VIS spectrophotometric analysisMore data for this Ligand-Target Pair