Compile Data Set for Download or QSAR

Found 9 hits of Enzyme Inhibition Constant Data   

TargetPurine nucleoside phosphorylase(Toxoplasma gondii)
CNRS UMR 7175

Curated by ChEMBL
LigandPNGBDBM50200328((4S,8R,9aS)-4-benzyl-8-(benzyloxy)-hexahydro-1H-py...)copy SMILEScopy InChI
Affinity DataKi:  8.00E+3nMAssay Description:Inhibition of Toxoplasma gondii purine nucleoside phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2PNDPubMed
TargetGroup 10 secretory phospholipase A2(Homo sapiens (Human))
CNRS UMR 7175

Curated by ChEMBL
LigandPNGBDBM50200327((E)-4-(6-Benzyl-1-methyl-4,7-dioxo-[1,3,5]triazepa...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human group 10 sPLA2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2PNDPubMed
TargetPhospholipase A2 group V(Homo sapiens (Human))
CNRS UMR 7175

Curated by ChEMBL
LigandPNGBDBM50200324((4S,7S)-4,7-dibenzyl-5-methyl-1,3,5-triazepane-2,6...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of human group 5 sPLA2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2PNDPubMed
TargetPhospholipase A2 group V(Homo sapiens (Human))
CNRS UMR 7175

Curated by ChEMBL
LigandPNGBDBM50200326(((S)-7-benzyl-3-tert-butoxycarbonylmethyl-5-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of human group 5 sPLA2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2PNDPubMed
TargetGroup 10 secretory phospholipase A2(Homo sapiens (Human))
CNRS UMR 7175

Curated by ChEMBL
LigandPNGBDBM50200325((S)-tert-butyl 2-(6-isopropyl-1-methyl-4,7-dioxo-1...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of human group 10 sPLA2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2PNDPubMed
TargetGroup 10 secretory phospholipase A2(Homo sapiens (Human))
CNRS UMR 7175

Curated by ChEMBL
LigandPNGBDBM50200326(((S)-7-benzyl-3-tert-butoxycarbonylmethyl-5-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of human group 10 sPLA2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2PNDPubMed
TargetPhospholipase A2 group V(Homo sapiens (Human))
CNRS UMR 7175

Curated by ChEMBL
LigandPNGBDBM50200325((S)-tert-butyl 2-(6-isopropyl-1-methyl-4,7-dioxo-1...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of human group 5 sPLA2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2PNDPubMed
TargetPhospholipase A2 group V(Homo sapiens (Human))
CNRS UMR 7175

Curated by ChEMBL
LigandPNGBDBM50200327((E)-4-(6-Benzyl-1-methyl-4,7-dioxo-[1,3,5]triazepa...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of human group 5 sPLA2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2PNDPubMed
TargetGroup 10 secretory phospholipase A2(Homo sapiens (Human))
CNRS UMR 7175

Curated by ChEMBL
LigandPNGBDBM50200324((4S,7S)-4,7-dibenzyl-5-methyl-1,3,5-triazepane-2,6...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of human group 10 sPLA2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2PNDPubMed
* indicates data uncertainty>20%