Compile Data Set for Download or QSAR
Found 12 with Last Name = 'therisod' and Initial = 'h'
TargetBeta-mannosidase(Homo sapiens (Human))
S.E.S.N.A.B., Pole Sciences et Technologie, Universit� de La Rochelle. therisod@icmo.u-psud.fr

Curated by ChEMBL
LigandPNGBDBM50070029((2Z)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-...)copy SMILEScopy InChI
Affinity DataKi:  25nMAssay Description:The compound was tested for its inhibitory activity against beta-mannosidaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PN9642PubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
S.E.S.N.A.B., Pole Sciences et Technologie, Universit� de La Rochelle. therisod@icmo.u-psud.fr

Curated by ChEMBL
LigandPNGBDBM50070029((2Z)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-...)copy SMILEScopy InChI
Affinity DataKi:  2.50E+3nMAssay Description:The compound was tested for its inhibitory activity against beta-glucosidaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PN9642PubMed
TargetTriosephosphate isomerase(Homo sapiens (Human))
UMR 8182

Curated by ChEMBL
LigandPNGBDBM50167777(2-(hydroxyamino)-2-oxoethyl dihydrogen phosphate |...)copy SMILEScopy InChI
Affinity DataKi:  3.00E+3nMAssay Description:Inhibition of triosephosphate isomeraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2639QK7PubMed
TargetTriosephosphate isomerase(Homo sapiens (Human))
UMR 8182

Curated by ChEMBL
LigandPNGBDBM50167775((Z)-2-amino-2-(hydroxyimino)ethyl hydrogen phospha...)copy SMILEScopy InChI
Affinity DataKi:  4.50E+3nMAssay Description:Inhibition of triosephosphate isomeraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2639QK7PubMed
TargetBeta-mannosidase(Homo sapiens (Human))
S.E.S.N.A.B., Pole Sciences et Technologie, Universit� de La Rochelle. therisod@icmo.u-psud.fr

Curated by ChEMBL
LigandPNGBDBM50070028(3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-...)copy SMILEScopy InChI
Affinity DataKi:  1.00E+4nMAssay Description:The compound was tested for its inhibitory activity against beta-mannosidaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PN9642PubMed
TargetBeta-mannosidase(Homo sapiens (Human))
S.E.S.N.A.B., Pole Sciences et Technologie, Universit� de La Rochelle. therisod@icmo.u-psud.fr

Curated by ChEMBL
LigandPNGBDBM50366566(CHEMBL610071)copy SMILEScopy InChI
Affinity DataKi:  1.70E+4nMAssay Description:The compound was tested for its inhibitory activity against beta-mannosidaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PN9642PubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
S.E.S.N.A.B., Pole Sciences et Technologie, Universit� de La Rochelle. therisod@icmo.u-psud.fr

Curated by ChEMBL
LigandPNGBDBM50366565(GLUCONOLACTONE)copy SMILEScopy InChI
Affinity DataKi:  3.00E+4nMAssay Description:The compound was tested for its inhibitory activity against beta-glucosidaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PN9642PubMed
TargetLysosomal alpha-glucosidase(Homo sapiens (Human))
S.E.S.N.A.B., Pole Sciences et Technologie, Universit� de La Rochelle. therisod@icmo.u-psud.fr

Curated by ChEMBL
LigandPNGBDBM50070029((2Z)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-...)copy SMILEScopy InChI
Affinity DataKi:  7.50E+4nMAssay Description:The compound was tested for its inhibitory activity against Alpha-glucosidaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PN9642PubMed
TargetTriosephosphate isomerase(Homo sapiens (Human))
UMR 8182

Curated by ChEMBL
LigandPNGBDBM50167772(2-hydrazinyl-2-oxoethyl hydrogen phosphate | CHEMB...)copy SMILEScopy InChI
Affinity DataKi:  1.11E+5nMAssay Description:Inhibition of triosephosphate isomeraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2639QK7PubMed
TargetTriosephosphate isomerase(Homo sapiens (Human))
UMR 8182

Curated by ChEMBL
LigandPNGBDBM50167776((2-Hydroxycarbamoyl-ethyl)-phosphonic acid | 3-(hy...)copy SMILEScopy InChI
Affinity DataKi:  1.60E+5nMAssay Description:Inhibition of triosephosphate isomeraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2639QK7PubMed
TargetTriosephosphate isomerase(Homo sapiens (Human))
UMR 8182

Curated by ChEMBL
LigandPNGBDBM50198029(CHEMBL390655 | hydrogen [1-azaniumyl-2-(hydroxycar...)copy SMILEScopy InChI
Affinity DataKi: >5.00E+5nMAssay Description:Inhibition of triosephosphate isomeraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2639QK7PubMed
TargetTriosephosphate isomerase(Homo sapiens (Human))
UMR 8182

Curated by ChEMBL
LigandPNGBDBM50198028(hydrogen 1-hydroxy-3-(hydroxyamino)-3-oxopropylpho...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of triosephosphate isomeraseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2639QK7PubMed