Found 127 with Last Name = 'ferreira' and Initial = 'vf' TargetReverse transcriptase(Human immunodeficiency virus 1)
Universidade Federal Fluminense
Curated by ChEMBL
Universidade Federal Fluminense
Curated by ChEMBL
Affinity DataKi: 500nMAssay Description:Inhibition of Human immunodeficiency virus 1 reverse transcriptaseMore data for this Ligand-Target Pair
TargetGlyceraldehyde-3-phosphate dehydrogenase, glycosomal(Trypanosoma cruzi)
Da Universidade De S£O Paulo
Curated by ChEMBL
Da Universidade De S£O Paulo
Curated by ChEMBL
Affinity DataKi: 1.60E+4nMAssay Description:Competitive inhibition of Trypanosoma cruzi glycosomal GAPDH NAD+ binding site by ITC methodMore data for this Ligand-Target Pair
TargetGlyceraldehyde-3-phosphate dehydrogenase, glycosomal(Trypanosoma cruzi)
Da Universidade De S£O Paulo
Curated by ChEMBL
Da Universidade De S£O Paulo
Curated by ChEMBL
Affinity DataKi: 1.71E+4nMAssay Description:Competitive inhibition of Trypanosoma cruzi glycosomal GAPDH NAD+ binding site by ITC methodMore data for this Ligand-Target Pair
TargetGlyceraldehyde-3-phosphate dehydrogenase, glycosomal(Trypanosoma cruzi)
Da Universidade De S£O Paulo
Curated by ChEMBL
Da Universidade De S£O Paulo
Curated by ChEMBL
Affinity DataKi: 1.87E+4nMAssay Description:Competitive inhibition of Trypanosoma cruzi glycosomal GAPDH NAD+ binding site by ITC methodMore data for this Ligand-Target Pair
TargetGlyceraldehyde-3-phosphate dehydrogenase, glycosomal(Trypanosoma cruzi)
Da Universidade De S£O Paulo
Curated by ChEMBL
Da Universidade De S£O Paulo
Curated by ChEMBL
Affinity DataKi: 2.95E+4nMAssay Description:Competitive inhibition of Trypanosoma cruzi glycosomal GAPDH NAD+ binding site by ITC methodMore data for this Ligand-Target Pair
TargetGlyceraldehyde-3-phosphate dehydrogenase, glycosomal(Trypanosoma cruzi)
Da Universidade De S£O Paulo
Curated by ChEMBL
Da Universidade De S£O Paulo
Curated by ChEMBL
Affinity DataKi: 3.23E+4nMAssay Description:Competitive inhibition of Trypanosoma cruzi glycosomal GAPDH NAD+ binding site by ITC methodMore data for this Ligand-Target Pair
Affinity DataKi: 3.36E+4nM ΔG°: -26.6kJ/mole IC50: 3.58E+4nMpH: 7.0 T: 2°CAssay Description:To test whether GCTs share a common binding pocket on PPA with acarbose, we performed an experiment according to the method of Yonetani and Theorell.More data for this Ligand-Target Pair
TargetGlyceraldehyde-3-phosphate dehydrogenase, glycosomal(Trypanosoma cruzi)
Da Universidade De S£O Paulo
Curated by ChEMBL
Da Universidade De S£O Paulo
Curated by ChEMBL
Affinity DataKi: 5.76E+4nMAssay Description:Competitive inhibition of Trypanosoma cruzi glycosomal GAPDH NAD+ binding site by ITC methodMore data for this Ligand-Target Pair
TargetGlyceraldehyde-3-phosphate dehydrogenase, glycosomal(Trypanosoma cruzi)
Da Universidade De S£O Paulo
Curated by ChEMBL
Da Universidade De S£O Paulo
Curated by ChEMBL
Affinity DataKi: 5.95E+4nMAssay Description:Competitive inhibition of Trypanosoma cruzi glycosomal GAPDH NAD+ binding site by ITC methodMore data for this Ligand-Target Pair
TargetGlyceraldehyde-3-phosphate dehydrogenase, glycosomal(Trypanosoma cruzi)
Da Universidade De S£O Paulo
Curated by ChEMBL
Da Universidade De S£O Paulo
Curated by ChEMBL
Affinity DataKi: 1.05E+5nMAssay Description:Non-competitive inhibition of Trypanosoma cruzi glycosomal GAPDH active site by ITC methodMore data for this Ligand-Target Pair
TargetGlyceraldehyde-3-phosphate dehydrogenase, glycosomal(Trypanosoma cruzi)
Da Universidade De S£O Paulo
Curated by ChEMBL
Da Universidade De S£O Paulo
Curated by ChEMBL
Affinity DataKi: 1.51E+5nMAssay Description:Non-competitive inhibition of Trypanosoma cruzi glycosomal GAPDH active site by ITC methodMore data for this Ligand-Target Pair
Affinity DataKi: 2.04E+5nM ΔG°: -21.9kJ/mole IC50: 8.89E+4nMpH: 7.0 T: 2°CAssay Description:To test whether GCTs share a common binding pocket on PPA with acarbose, we performed an experiment according to the method of Yonetani and Theorell.More data for this Ligand-Target Pair
Affinity DataKi: 2.34E+5nM ΔG°: -21.6kJ/mole IC50: 1.25E+5nMpH: 7.0 T: 2°CAssay Description:To test whether GCTs share a common binding pocket on PPA with acarbose, we performed an experiment according to the method of Yonetani and Theorell.More data for this Ligand-Target Pair
TargetGlyceraldehyde-3-phosphate dehydrogenase, glycosomal(Trypanosoma cruzi)
Da Universidade De S£O Paulo
Curated by ChEMBL
Da Universidade De S£O Paulo
Curated by ChEMBL
Affinity DataKi: 3.05E+5nMAssay Description:Non-competitive inhibition of Trypanosoma cruzi glycosomal GAPDH active site by ITC methodMore data for this Ligand-Target Pair
Affinity DataKi: 3.42E+5nM ΔG°: -20.6kJ/mole IC50: 1.50E+5nMpH: 7.0 T: 2°CAssay Description:To test whether GCTs share a common binding pocket on PPA with acarbose, we performed an experiment according to the method of Yonetani and Theorell.More data for this Ligand-Target Pair
Affinity DataKi: 7.80E+5nM ΔG°: -18.5kJ/mole IC50: 3.61E+5nMpH: 7.0 T: 2°CAssay Description:To test whether GCTs share a common binding pocket on PPA with acarbose, we performed an experiment according to the method of Yonetani and Theorell.More data for this Ligand-Target Pair
Affinity DataKi: 1.01E+6nM ΔG°: -17.8kJ/mole IC50: 3.56E+5nMpH: 7.0 T: 2°CAssay Description:To test whether GCTs share a common binding pocket on PPA with acarbose, we performed an experiment according to the method of Yonetani and Theorell.More data for this Ligand-Target Pair
Affinity DataIC50: 5.30nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as inhibition of ATP-induced ethidium iodide uptake preincubated for 10...More data for this Ligand-Target Pair
Affinity DataIC50: 6.60nMAssay Description:Tested for inhibitory potency against rat liver microsomal squalene synthaseMore data for this Ligand-Target Pair
Affinity DataIC50: 20nMAssay Description:In vitro thromboxane A2 receptor antagonism through inhibition of U-46619 induced platelet aggregation in human whole bloodMore data for this Ligand-Target Pair
Affinity DataIC50: 20nMAssay Description:In vitro thromboxane A2 receptor antagonism through inhibition of U-46619 induced platelet aggregation in human whole bloodMore data for this Ligand-Target Pair
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Instituto De Tecnologia Em F£Rmacos
Curated by ChEMBL
Instituto De Tecnologia Em F£Rmacos
Curated by ChEMBL
Affinity DataIC50: 20nMAssay Description:Tested for inhibitory potency against rat liver microsomal squalene synthaseMore data for this Ligand-Target Pair
Affinity DataIC50: 22nMAssay Description:Antagonist activity at human P2X7R expressed in HEK293 cells assessed as inhibition of ATP-induced ethidium iodide uptake preincubated for 10 mins fo...More data for this Ligand-Target Pair
Affinity DataIC50: 23nMAssay Description:Antagonist activity at P2X7R in Swiss Webster mouse peritoneal macrophages assessed as inhibition of ATP-induced propidium iodide uptake preincubated...More data for this Ligand-Target Pair
Affinity DataIC50: 37nMAssay Description:In vitro thromboxane A2 receptor antagonism through inhibition of U-46619 induced contraction of rat isolated thoracic aortic stripMore data for this Ligand-Target Pair
Affinity DataIC50: 41nMAssay Description:Antagonist activity at P2X7 receptor in Swiss mouse peritoneal macrophages assessed as inhibition of BzATP-induced current at holding potential of -6...More data for this Ligand-Target Pair
Affinity DataIC50: 47nMAssay Description:Antagonist activity at P2X7 receptor in Swiss mouse peritoneal macrophages assessed as inhibition of BzATP-induced current at holding potential of -6...More data for this Ligand-Target Pair
Affinity DataIC50: 48nMAssay Description:Antagonist activity at P2X7R in Swiss Webster mouse peritoneal macrophages assessed as inhibition of ATP-induced propidium iodide uptake preincubated...More data for this Ligand-Target Pair
Affinity DataIC50: 59nMAssay Description:Antagonist activity at P2X7 receptor in Swiss mouse peritoneal macrophages assessed as inhibition of BzATP-induced ethidium iodide uptake after 30 mi...More data for this Ligand-Target Pair
Affinity DataIC50: 63nMAssay Description:In vitro thromboxane A2 receptor antagonism through inhibition of U-46619 induced contraction of rat isolated thoracic aortic stripMore data for this Ligand-Target Pair
Affinity DataIC50: 67nMAssay Description:Tested for inhibitory potency against rat liver microsomal squalene synthaseMore data for this Ligand-Target Pair
Affinity DataIC50: 67nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as inhibition of ATP-induced IL-1beta release preincubated for 30 mins ...More data for this Ligand-Target Pair
Affinity DataIC50: 69nMAssay Description:In vitro thromboxane A2 receptor antagonism through inhibition of U-46619 induced contraction of rat isolated thoracic aortic stripMore data for this Ligand-Target Pair
Affinity DataIC50: 71nMAssay Description:Antagonist activity at human P2X7R expressed in HEK293 cells assessed as inhibition of ATP-induced ethidium iodide uptake preincubated for 10 mins fo...More data for this Ligand-Target Pair
Affinity DataIC50: 81nMAssay Description:Antagonist activity at P2X7 receptor in Swiss mouse peritoneal macrophages assessed as inhibition of ATP-induced current at holding potential of -60 ...More data for this Ligand-Target Pair
Affinity DataIC50: 82nMAssay Description:Evaluated for the antagonistic activity against Serotonin 5-hydroxytryptamine 4 receptor in non-electrically stimulated guinea-pig ileum.More data for this Ligand-Target Pair
Affinity DataIC50: 83nMAssay Description:Antagonist activity at P2X7 receptor in Swiss mouse peritoneal macrophages assessed as inhibition of ATP-induced propidium iodide uptake after 25 min...More data for this Ligand-Target Pair
Affinity DataIC50: 86nMAssay Description:In vitro thromboxane A2 receptor antagonism through inhibition of U-46619 induced platelet aggregation in human whole bloodMore data for this Ligand-Target Pair
Affinity DataIC50: 89nMAssay Description:Tested for inhibitory potency against rat liver microsomal squalene synthaseMore data for this Ligand-Target Pair
Affinity DataIC50: 91nMAssay Description:In vitro thromboxane A2 receptor antagonism through inhibition of U-46619 induced contraction of rat isolated thoracic aortic stripMore data for this Ligand-Target Pair
Affinity DataIC50: 96nMAssay Description:In vitro thromboxane A2 receptor antagonism through inhibition of U-46619 induced contraction of rat isolated thoracic aortic stripMore data for this Ligand-Target Pair
TargetGlyceraldehyde-3-phosphate dehydrogenase(Homo sapiens (Human))
Universidade Federal De Minas Gerais
Curated by ChEMBL
Universidade Federal De Minas Gerais
Curated by ChEMBL
Affinity DataIC50: 100nMAssay Description:Inhibitory concentration of compound against glyceraldehyde-3-phosphate dehydrogenase was determinedMore data for this Ligand-Target Pair
Affinity DataIC50: 103nMAssay Description:Antagonist activity at human P2X7R expressed in HEK293 cells assessed as inhibition of ATP-induced ethidium iodide uptake preincubated for 5 mins fol...More data for this Ligand-Target Pair
Affinity DataIC50: 103nMAssay Description:In vitro thromboxane A2 receptor antagonism through inhibition of U-46619 induced platelet aggregation in human whole bloodMore data for this Ligand-Target Pair
Affinity DataIC50: 103nMAssay Description:In vitro thromboxane A2 receptor antagonism through inhibition of U-46619 induced contraction of rat isolated thoracic aortic stripMore data for this Ligand-Target Pair
Affinity DataIC50: 107nMAssay Description:Antagonist activity at P2X7 receptor in Swiss mouse peritoneal macrophages assessed as inhibition of ATP-induced propidium iodide uptake after 25 min...More data for this Ligand-Target Pair
Affinity DataIC50: 108nMAssay Description:In vitro thromboxane A2 receptor antagonism through inhibition of U-46619 induced contraction of rat isolated thoracic aortic stripMore data for this Ligand-Target Pair
Affinity DataIC50: 109nMAssay Description:Antagonist activity at human P2X7R expressed in HEK293 cells assessed as inhibition of ATP-induced ethidium iodide uptake preincubated for 10 mins fo...More data for this Ligand-Target Pair
Affinity DataIC50: 109nMAssay Description:Antagonist activity at P2X7 receptor in Swiss mouse peritoneal macrophages assessed as inhibition of ATP-induced current at holding potential of -60 ...More data for this Ligand-Target Pair
Affinity DataIC50: 112nMAssay Description:Tested for inhibitory potency against rat liver microsomal squalene synthaseMore data for this Ligand-Target Pair
