Compile Data Set for Download or QSAR
maximum 50k data
Found 63 Enz. Inhib. hit(s) with all data for entry = 2753
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24206(2-{4-[2-(azepan-1-yl)ethoxy]phenoxy}-1,3-benzoxazo...)
Affinity DataIC50:  4nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24216(1-{2-[4-(1,3-benzoxazol-2-yloxy)phenoxy]ethyl}-4-p...)
Affinity DataIC50:  6nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24199(2-{4-[2-(pyrrolidin-1-yl)ethoxy]phenoxy}-1,3-benzo...)
Affinity DataIC50:  7nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24224(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenyl]ethyl}pip...)
Affinity DataIC50:  8nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24238(Benzthiazole compound, 33p | N-(1-{[4-(1,3-benzoth...)
Affinity DataIC50:  8nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24212(1-{2-[4-(1,3-benzoxazol-2-yloxy)phenoxy]ethyl}pipe...)
Affinity DataIC50:  9nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24235(3-(1-{[4-(1,3-benzothiazol-2-yloxy)phenyl]methyl}p...)
Affinity DataIC50:  10nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24203(2-{4-[2-(piperidin-1-yl)ethoxy]phenoxy}-1,3-benzox...)
Affinity DataIC50:  11nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24239(1-{[4-(1,3-benzothiazol-2-yloxy)phenyl]methyl}pipe...)
Affinity DataIC50:  11nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24222(3-(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenoxy]ethyl...)
Affinity DataIC50:  11nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24236(Benzthiazole compound, 33n | N-(1-{[4-(1,3-benzoth...)
Affinity DataIC50:  12nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24234(1-(1-{[4-(1,3-benzothiazol-2-yloxy)phenyl]methyl}p...)
Affinity DataIC50:  12nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24227(1-(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenyl]ethyl}...)
Affinity DataIC50:  13nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24218(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenoxy]ethyl}pi...)
Affinity DataIC50:  13nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24215((1-{2-[4-(1,3-benzothiazol-2-yloxy)phenoxy]ethyl}p...)
Affinity DataIC50:  13nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24214((1-{2-[4-(1,3-benzoxazol-2-yloxy)phenoxy]ethyl}pip...)
Affinity DataIC50:  14nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24201(2-{4-[2-(pyrrolidin-1-yl)ethoxy]phenoxy}-1,3-benzo...)
Affinity DataIC50:  14nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24220(1-(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenoxy]ethyl...)
Affinity DataIC50:  16nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24223(2-{4-[2-(piperidin-1-yl)ethyl]phenoxy}-1,3-benzoth...)
Affinity DataIC50:  17nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24233(1-{[4-(1,3-benzothiazol-2-yloxy)phenyl]methyl}pipe...)
Affinity DataIC50:  17nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24237(Benzthiazole compound, 33o | [(1-{[4-(1,3-benzothi...)
Affinity DataIC50:  21nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24240(2-{4-[3-(piperidin-1-yl)propoxy]phenoxy}-1,3-benzo...)
Affinity DataIC50:  27nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24225(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenyl]ethyl}pip...)
Affinity DataIC50:  28nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24228(3-(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenyl]ethyl}...)
Affinity DataIC50:  29nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24213(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenoxy]ethyl}pi...)
Affinity DataIC50:  31nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24232(1-{[4-(1,3-benzothiazol-2-yloxy)phenyl]methyl}pipe...)
Affinity DataIC50:  34nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24229(Benzthiazole compound, 27n | N-(1-{2-[4-(1,3-benzo...)
Affinity DataIC50:  35nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24230(Benzthiazole compound, 27o | [(1-{2-[4-(1,3-benzot...)
Affinity DataIC50:  50nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24204(2-{4-[2-(piperidin-1-yl)ethoxy]phenoxy}-1,3-benzot...)
Affinity DataIC50:  54nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24209(2-{4-[2-(morpholin-4-yl)ethoxy]phenoxy}-1,3-benzox...)
Affinity DataIC50:  58nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24231(2-[4-(piperidin-1-ylmethyl)phenoxy]-1,3-benzothiaz...)
Affinity DataIC50:  59nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24219(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenoxy]ethyl}pi...)
Affinity DataIC50:  66nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24207(2-{4-[2-(azepan-1-yl)ethoxy]phenoxy}-1,3-benzothia...)
Affinity DataIC50:  66nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24217(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenoxy]ethyl}-4...)
Affinity DataIC50:  66nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24221(1-(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenoxy]ethyl...)
Affinity DataIC50:  70nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24202(2-{4-[2-(pyrrolidin-1-yl)ethoxy]phenoxy}-1H-1,3-be...)
Affinity DataIC50:  84nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24241(2-{4-[3-(piperidin-1-yl)propoxy]phenoxy}-1,3-benzo...)
Affinity DataIC50:  87nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24205(2-{4-[2-(piperidin-1-yl)ethoxy]phenoxy}-1H-1,3-ben...)
Affinity DataIC50:  110nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24208(2-{4-[2-(azepan-1-yl)ethoxy]phenoxy}-1H-1,3-benzod...)
Affinity DataIC50:  140nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24210(4-{2-[4-(1,3-benzothiazol-2-yloxy)phenoxy]ethyl}mo...)
Affinity DataIC50:  350nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24228(3-(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenyl]ethyl}...)
Affinity DataIC50:  500nMAssay Description:Compounds were assessed for their ability to displace [3H]astemizole using membranes from HEK-293 cells expressing the hERG K+ channel.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24242(2-{4-[3-(piperidin-1-yl)propoxy]phenoxy}-1H-1,3-be...)
Affinity DataIC50:  710nMT: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24203(2-{4-[2-(piperidin-1-yl)ethoxy]phenoxy}-1,3-benzox...)
Affinity DataIC50:  1.00E+3nMpH: 7.4 T: 2°CAssay Description:Compounds were assessed for their ability to displace [3H]astemizole using membranes from HEK-293 cells expressing the hERG K+ channel.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24227(1-(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenyl]ethyl}...)
Affinity DataIC50:  1.00E+3nMAssay Description:Compounds were assessed for their ability to displace [3H]astemizole using membranes from HEK-293 cells expressing the hERG K+ channel.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24221(1-(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenoxy]ethyl...)
Affinity DataIC50:  1.80E+3nMT: 2°CAssay Description:Compounds were assessed for their ability to displace [3H]astemizole using membranes from HEK-293 cells expressing the hERG K+ channel.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24223(2-{4-[2-(piperidin-1-yl)ethyl]phenoxy}-1,3-benzoth...)
Affinity DataIC50:  2.00E+3nMpH: 7.4 T: 2°CAssay Description:Compounds were assessed for their ability to displace [3H]astemizole using membranes from HEK-293 cells expressing the hERG K+ channel.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24222(3-(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenoxy]ethyl...)
Affinity DataIC50:  2.70E+3nMT: 2°CAssay Description:Compounds were assessed for their ability to displace [3H]astemizole using membranes from HEK-293 cells expressing the hERG K+ channel.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24220(1-(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenoxy]ethyl...)
Affinity DataIC50:  2.70E+3nMT: 2°CAssay Description:Compounds were assessed for their ability to displace [3H]astemizole using membranes from HEK-293 cells expressing the hERG K+ channel.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24211(4-{2-[4-(1H-1,3-benzodiazol-2-yloxy)phenoxy]ethyl}...)
Affinity DataIC50:  3.00E+3nMpH: 7.4 T: 2°CAssay Description:Recombinant human LTA4H was incubated with various concentrations of test compound for 10 min at room temperature in assay buffer, and the substrate,...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM24224(1-{2-[4-(1,3-benzothiazol-2-yloxy)phenyl]ethyl}pip...)
Affinity DataIC50:  3.00E+3nMpH: 7.4 T: 2°CAssay Description:Compounds were assessed for their ability to displace [3H]astemizole using membranes from HEK-293 cells expressing the hERG K+ channel.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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