Report error Found 635 of ic50 data for polymerid = 1192,50007428,50007429
Affinity DataIC50: 0.140nMAssay Description:Inhibition of carbonic anhydrase-1 in human erythrocyte membranes assessed as reduction in H+ release using CO2 as substrate by bromine thymol blue i...More data for this Ligand-Target Pair
Affinity DataIC50: 0.210nMAssay Description:Inhibition of carbonic anhydrase-1 in human erythrocyte membranes assessed as reduction in H+ release using CO2 as substrate by bromine thymol blue i...More data for this Ligand-Target Pair
Affinity DataIC50: 0.280nMAssay Description:Inhibition of carbonic anhydrase-1 in human erythrocyte membranes assessed as reduction in H+ release using CO2 as substrate by bromine thymol blue i...More data for this Ligand-Target Pair
Affinity DataIC50: 0.288nMAssay Description:Inhibition of human erythrocyte carbonic anhydrase-1More data for this Ligand-Target Pair
Affinity DataIC50: 0.290nMAssay Description:Inhibition of carbonic anhydrase-1 in human erythrocyte membranes assessed as reduction in H+ release using CO2 as substrate by bromine thymol blue i...More data for this Ligand-Target Pair
Affinity DataIC50: 0.290nMAssay Description:Inhibition of carbonic anhydrase-1 in human erythrocyte membranes assessed as reduction in H+ release using CO2 as substrate by bromine thymol blue i...More data for this Ligand-Target Pair
Affinity DataIC50: 0.346nMAssay Description:Inhibition of human erythrocyte carbonic anhydrase-1More data for this Ligand-Target Pair
Affinity DataIC50: 0.450nMAssay Description:Inhibition of carbonic anhydrase-1 in human erythrocyte membranes assessed as reduction in H+ release using CO2 as substrate by bromine thymol blue i...More data for this Ligand-Target Pair
Affinity DataKi: 0.442nM ΔG°: -53.4kJ/mole IC50: 0.466nMpH: 7.4 T: 2°CAssay Description:Esterase activity assay was performed based on the method of by Verpoorte et al. [Verpoorte et al., J. Biol. Chem., 242:4221-4229] as described in pr...More data for this Ligand-Target Pair
Affinity DataKi: 0.475nM ΔG°: -53.2kJ/mole IC50: 0.506nMpH: 7.4 T: 2°CAssay Description:Esterase activity assay was performed based on the method of by Verpoorte et al. [Verpoorte et al., J. Biol. Chem., 242:4221-4229] as described in pr...More data for this Ligand-Target Pair
Affinity DataIC50: 0.518nMAssay Description:Inhibition of human erythrocyte carbonic anhydrase-1More data for this Ligand-Target Pair
Affinity DataIC50: 0.535nMAssay Description:Inhibition of human erythrocyte carbonic anhydrase-1More data for this Ligand-Target Pair
Affinity DataKi: 0.529nM ΔG°: -52.9kJ/mole IC50: 0.537nMpH: 7.4 T: 2°CAssay Description:Esterase activity assay was performed based on the method of by Verpoorte et al. [Verpoorte et al., J. Biol. Chem., 242:4221-4229] as described in pr...More data for this Ligand-Target Pair
Affinity DataIC50: 0.556nMAssay Description:Inhibition of human erythrocyte carbonic anhydrase-1More data for this Ligand-Target Pair
Affinity DataIC50: 0.560nMAssay Description:Inhibition of carbonic anhydrase-1 in human erythrocyte membranes assessed as reduction in H+ release using CO2 as substrate by bromine thymol blue i...More data for this Ligand-Target Pair
Affinity DataIC50: 0.570nMAssay Description:Inhibition of carbonic anhydrase-1 in human erythrocyte membranes assessed as reduction in H+ release using CO2 as substrate by bromine thymol blue i...More data for this Ligand-Target Pair
Affinity DataKi: 0.405nM ΔG°: -53.6kJ/mole IC50: 0.573nMpH: 7.4 T: 2°CAssay Description:Esterase activity assay was performed based on the method of by Verpoorte et al. [Verpoorte et al., J. Biol. Chem., 242:4221-4229] as described in pr...More data for this Ligand-Target Pair
Affinity DataKi: 0.523nM ΔG°: -53.0kJ/mole IC50: 0.579nMpH: 7.4 T: 2°CAssay Description:Esterase activity assay was performed based on the method of by Verpoorte et al. [Verpoorte et al., J. Biol. Chem., 242:4221-4229] as described in pr...More data for this Ligand-Target Pair
Affinity DataKi: 0.501nM ΔG°: -53.1kJ/mole IC50: 0.597nMpH: 7.4 T: 2°CAssay Description:Esterase activity assay was performed based on the method of by Verpoorte et al. [Verpoorte et al., J. Biol. Chem., 242:4221-4229] as described in pr...More data for this Ligand-Target Pair
Affinity DataKi: 0.605nM ΔG°: -52.6kJ/mole IC50: 0.597nMpH: 7.4 T: 2°CAssay Description:Esterase activity assay was performed based on the method of by Verpoorte et al. [Verpoorte et al., J. Biol. Chem., 242:4221-4229] as described in pr...More data for this Ligand-Target Pair
Affinity DataKi: 0.469nM ΔG°: -53.2kJ/mole IC50: 0.606nMpH: 7.4 T: 2°CAssay Description:Esterase activity assay was performed based on the method of by Verpoorte et al. [Verpoorte et al., J. Biol. Chem., 242:4221-4229] as described in pr...More data for this Ligand-Target Pair
Affinity DataKi: 0.549nM ΔG°: -52.9kJ/mole IC50: 0.611nMpH: 7.4 T: 2°CAssay Description:Esterase activity assay was performed based on the method of by Verpoorte et al. [Verpoorte et al., J. Biol. Chem., 242:4221-4229] as described in pr...More data for this Ligand-Target Pair
Affinity DataKi: 0.518nM ΔG°: -53.0kJ/mole IC50: 0.619nMpH: 7.4 T: 2°CAssay Description:Esterase activity assay was performed based on the method of by Verpoorte et al. [Verpoorte et al., J. Biol. Chem., 242:4221-4229] as described in pr...More data for this Ligand-Target Pair
Affinity DataIC50: 0.624nMAssay Description:Inhibition of human erythrocyte carbonic anhydrase-1More data for this Ligand-Target Pair
Affinity DataKi: 0.513nM ΔG°: -53.0kJ/mole IC50: 0.639nMpH: 7.4 T: 2°CAssay Description:Esterase activity assay was performed based on the method of by Verpoorte et al. [Verpoorte et al., J. Biol. Chem., 242:4221-4229] as described in pr...More data for this Ligand-Target Pair
Affinity DataKi: 0.603nM ΔG°: -52.6kJ/mole IC50: 0.650nMpH: 7.4 T: 2°CAssay Description:Esterase activity assay was performed based on the method of by Verpoorte et al. [Verpoorte et al., J. Biol. Chem., 242:4221-4229] as described in pr...More data for this Ligand-Target Pair
Affinity DataKi: 0.595nM ΔG°: -52.7kJ/mole IC50: 0.655nMpH: 7.4 T: 2°CAssay Description:Esterase activity assay was performed based on the method of by Verpoorte et al. [Verpoorte et al., J. Biol. Chem., 242:4221-4229] as described in pr...More data for this Ligand-Target Pair
Affinity DataIC50: 0.677nMAssay Description:Inhibition of human erythrocyte carbonic anhydrase-1More data for this Ligand-Target Pair
Affinity DataIC50: 0.699nMAssay Description:Inhibition of human erythrocyte carbonic anhydrase-1More data for this Ligand-Target Pair
Affinity DataKi: 0.636nM ΔG°: -52.5kJ/mole IC50: 0.711nMpH: 7.4 T: 2°CAssay Description:Esterase activity assay was performed based on the method of by Verpoorte et al. [Verpoorte et al., J. Biol. Chem., 242:4221-4229] as described in pr...More data for this Ligand-Target Pair
Affinity DataIC50: 0.770nMAssay Description:Inhibition of carbonic anhydrase-1 in human erythrocyte membranes assessed as reduction in H+ release using CO2 as substrate by bromine thymol blue i...More data for this Ligand-Target Pair
Affinity DataIC50: 0.903nMAssay Description:Inhibition of human erythrocyte carbonic anhydrase-1More data for this Ligand-Target Pair
Affinity DataKi: 0.747nM ΔG°: -52.1kJ/mole IC50: 0.996nMpH: 7.4 T: 2°CAssay Description:Esterase activity assay was performed based on the method of by Verpoorte et al. [Verpoorte et al., J. Biol. Chem., 242:4221-4229] as described in pr...More data for this Ligand-Target Pair
3D Structure (crystal)
Affinity DataIC50: 1.70nMAssay Description:Inhibition of human erythrocyte carbonic anhydrase-1More data for this Ligand-Target Pair
Affinity DataIC50: 2.10nMAssay Description:Inhibition of full length carbonic anhydrase-1 in human erythrocytesMore data for this Ligand-Target Pair
Affinity DataIC50: 3.10nMAssay Description:Inhibition of full length carbonic anhydrase-1 in human erythrocytesMore data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of human CA1 by stopped-flow assayMore data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of human CA1 by spectrophotometer based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of human CA1 by spectrophotometer based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of human CA1 by spectrophotometer based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of human CA1 by spectrophotometer based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of human CA1 by spectrophotometer based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of human CA1 by spectrophotometer based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of human CA1 by spectrophotometer based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of human CA1More data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of human CA1More data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of human CA1More data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of human CA1More data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of human CA1More data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of human CA1More data for this Ligand-Target Pair
