Compile Data Set for Download or QSAR
Found 115 with Last Name = 'stec' and Initial = 'j'
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50350513(CHEMBL1812069)copy SMILEScopy InChI
Affinity DataKi:  35nMAssay Description:Inhibition of Fragile histidine triad prorein hydrolytic activityMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79GMPubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50350514(CHEMBL1812068)copy SMILEScopy InChI
Affinity DataKi:  35nMAssay Description:Inhibition of Fragile histidine triad prorein hydrolytic activityMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79GMPubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50350515(CHEMBL1812067)copy SMILEScopy InChI
Affinity DataKi:  35nMAssay Description:Inhibition of Fragile histidine triad prorein hydrolytic activityMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79GMPubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50350516(CHEMBL1812066)copy SMILEScopy InChI
Affinity DataKi:  35nMAssay Description:Inhibition of Fragile histidine triad prorein hydrolytic activityMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79GMPubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50350512(CHEMBL1812070)copy SMILEScopy InChI
Affinity DataKi:  35nMAssay Description:Inhibition of Fragile histidine triad prorein hydrolytic activityMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79GMPubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81576(AppppA analog, 6 (X=S))copy SMILEScopy InChI
Affinity DataKi:  35nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81584(AppppA analog, 12 (X=S))copy SMILEScopy InChI
Affinity DataKi:  40nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81586(AppppA analog, 13 (X=S))copy SMILEScopy InChI
Affinity DataKi:  65nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81590(AppppA analog, 15 (X=S))copy SMILEScopy InChI
Affinity DataKi:  78nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81593(AppppA analog, 17 (X=S))copy SMILEScopy InChI
Affinity DataKi:  110nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81575(AppppA analog, 5 (X=S))copy SMILEScopy InChI
Affinity DataKi:  220nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81580(AppppA analog, 9 (X=S))copy SMILEScopy InChI
Affinity DataKi:  230nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81592(AppppA analog, 17 (X=O))copy SMILEScopy InChI
Affinity DataKi:  420nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81588(AppppA analog, 14 (X=S))copy SMILEScopy InChI
Affinity DataKi:  700nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81587(AppppA analog, 14 (X=O))copy SMILEScopy InChI
Affinity DataKi:  900nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81589(AppppA analog, 15 (X=O))copy SMILEScopy InChI
Affinity DataKi:  1.50E+3nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81574(AppppA analog, 5 (X=O))copy SMILEScopy InChI
Affinity DataKi:  1.50E+3nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81583(AppppA analog, 12 (X=O))copy SMILEScopy InChI
Affinity DataKi:  1.50E+3nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81570(AppppA analog, 1 (X=O))copy SMILEScopy InChI
Affinity DataKi:  2.60E+3nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81571(AppppA analog, 2 (X=S))copy SMILEScopy InChI
Affinity DataKi:  2.60E+3nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81591(AppppA analog, 16 (X=S))copy SMILEScopy InChI
Affinity DataKi:  2.70E+3nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81579(AppppA analog, 8 (X=S))copy SMILEScopy InChI
Affinity DataKi:  3.00E+3nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81585(AppppA analog, 13 (X=O))copy SMILEScopy InChI
Affinity DataKi:  3.20E+3nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81581(AppppA analog, 10 (X=S))copy SMILEScopy InChI
Affinity DataKi:  3.30E+3nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81577(AppppA analog, 6 (X=O))copy SMILEScopy InChI
Affinity DataKi:  4.70E+3nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81582(AppppA analog, 11 (X=S))copy SMILEScopy InChI
Affinity DataKi:  5.20E+3nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81578(AppppA analog, 7 (X=S))copy SMILEScopy InChI
Affinity DataKi:  7.60E+4nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81573(AppppA analog, 4 (X=S))copy SMILEScopy InChI
Affinity DataKi:  8.60E+4nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetBis(5'-adenosyl)-triphosphatase(Homo sapiens (Human))
Polish Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM81572(AppppA analog, 3 (X=S))copy SMILEScopy InChI
Affinity DataKi:  8.60E+4nMAssay Description:Inhibition assay using Fhit with ApppBODIPY.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2445JZ9PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM50174768(5‐chloro‐2‐(2‐chloro‐...)copy SMILEScopy InChI
Affinity DataIC50: 3nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM25407(2‐(2,4‐dichlorophenoxy)‐5‐...)copy SMILEScopy InChI
Affinity DataIC50: 8nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM50174760(2‐[4‐(benzylamino)‐2‐chlor...)copy SMILEScopy InChI
Affinity DataIC50: 13nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM8726(5-chloro-2-(2,4-dichlorophenoxy)phenol | CHEMBL849...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Inhibition of Toxoplasma gondii enoyl acyl-carrier protein reductaseMore data for this Ligand-Target Pair
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM8726(5-chloro-2-(2,4-dichlorophenoxy)phenol | CHEMBL849...)copy SMILEScopy InChI
Affinity DataIC50: 15nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM50174774(2‐({[3‐chloro‐4‐(4‐c...)copy SMILEScopy InChI
Affinity DataIC50: 16nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM119865(6‐chloro‐3‐(2,4‐dichloroph...)copy SMILEScopy InChI
Affinity DataIC50: 18nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM50435717(CHEMBL2392450 | N‐{[4‐(2,4‐dichl...)copy SMILEScopy InChI
Affinity DataIC50: 19nMAssay Description:Inhibition of Toxoplasma gondii enoyl acyl-carrier protein reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8GZ7PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM50435717(CHEMBL2392450 | N‐{[4‐(2,4‐dichl...)copy SMILEScopy InChI
Affinity DataIC50: 19nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM119866(3‐chloro‐6‐(2,4‐dichloroph...)copy SMILEScopy InChI
Affinity DataIC50: 23nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM25403(4‐(2,4‐dichlorophenoxy)‐3‐...)copy SMILEScopy InChI
Affinity DataIC50: 24nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM119867(5‐chloro‐2‐[2‐chloro‐...)copy SMILEScopy InChI
Affinity DataIC50: 26nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM50435720(CHEMBL2392447)copy SMILEScopy InChI
Affinity DataIC50: 29nMAssay Description:Inhibition of Toxoplasma gondii enoyl acyl-carrier protein reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8GZ7PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM50431922(5‐chloro‐2‐[2‐chloro‐...)copy SMILEScopy InChI
Affinity DataIC50: 30nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM119869(5‐chloro‐2‐{2‐chloro‐...)copy SMILEScopy InChI
Affinity DataIC50: 31nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM119870(N‐{[3‐chloro‐4‐(4‐ch...)copy SMILEScopy InChI
Affinity DataIC50: 33nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM50435719(CHEMBL2392448)copy SMILEScopy InChI
Affinity DataIC50: 34nMAssay Description:Inhibition of Toxoplasma gondii enoyl acyl-carrier protein reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8GZ7PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM50431923(5‐chloro‐2‐(naphthalen‐2&#...)copy SMILEScopy InChI
Affinity DataIC50: 41nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM119868(2‐{4‐[(4‐butyl‐1,2,3‐...)copy SMILEScopy InChI
Affinity DataIC50: 43nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM50431920(5‐(4‐chloro‐2‐hydroxypheno...)copy SMILEScopy InChI
Affinity DataIC50: 58nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
Johns Hopkins Bloomberg School of Public Health

LigandPNGBDBM119871(N‐{[3‐chloro‐4‐(4‐ch...)copy SMILEScopy InChI
Affinity DataIC50: 100nMpH: 7.5Assay Description:The reaction mixture (100 µL) contained 100 µM crotonyl-CoA, 1 µL DMSO (or compounds dissolved in DMSO), 5 nM TgENR, 100 mM sodium/pot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6J27PubMed
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