Compile Data Set for Download or QSAR
Found 18 with Last Name = 'campitelli' and Initial = 'mr'
TargetMyosin light chain kinase, smooth muscle(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM15236(3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-chr...)copy SMILEScopy InChI
Affinity DataKi:  1.70E+3nMAssay Description:Inhibition of MLCKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GHFPubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM59087(CHEMBL258765 | Fasca-plysi | Fascaplysin)copy SMILEScopy InChI
Affinity DataIC50: 350nMAssay Description:Inhibition of CDK4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GHFPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM19459(5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 740nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GHFPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM50241222(CHEMBL242740 | Tectorigenin | psi-tectorigenin)copy SMILEScopy InChI
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GHFPubMed
TargetCyclin-dependent kinase 6(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM59087(CHEMBL258765 | Fasca-plysi | Fascaplysin)copy SMILEScopy InChI
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of CDK6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GHFPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM50042949((E)-1-(2,4-dihydroxyphenyl)-3-(3,4-dihydroxyphenyl...)copy SMILEScopy InChI
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GHFPubMed
TargetMyosin light chain kinase, smooth muscle(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM50045936((E)-4-(3,5-dihydroxystyryl)benzene-1,2-diol | (E)-...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of MLCKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GHFPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM7460(2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chrome...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of LCKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GHFPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM50042949((E)-1-(2,4-dihydroxyphenyl)-3-(3,4-dihydroxyphenyl...)copy SMILEScopy InChI
Affinity DataIC50: 6.50E+4nMAssay Description:Inhibition of c-SrcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GHFPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM50045936((E)-4-(3,5-dihydroxystyryl)benzene-1,2-diol | (E)-...)copy SMILEScopy InChI
Affinity DataIC50: 8.20E+4nMAssay Description:Inhibition of LCKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GHFPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM50250286(CHEMBL490510 | Marein)copy SMILEScopy InChI
Affinity DataIC50: 1.90E+7nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GHFPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM23446(3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)prop...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+7nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GHFPubMed
TargetCathepsin B(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50391540(CHEMBL2147469)copy SMILEScopy InChI
Affinity DataEC50:  200nMAssay Description:Inhibition of cathepsin B using Z-Phe-Arg-MCA as substrate incubated for 10 mins prior to substrate addition measured after 30 mins by fluorimetric a...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z03979PubMed
TargetPlasminogen(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50391540(CHEMBL2147469)copy SMILEScopy InChI
Affinity DataEC50:  4.90E+3nMAssay Description:Inhibition of plasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z03979PubMed
TargetProthrombin(Bos taurus (Bovine))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50391541(CHEMBL2147467)copy SMILEScopy InChI
Affinity DataEC50:  4.90E+3nMAssay Description:Inhibition of bovine thrombin using Bz-Phe-Val-Arg-pNA as substrate incubated for 5 mins prior to substrate addition measured after 30 mins by fluori...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z03979PubMed
TargetProthrombin(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50391540(CHEMBL2147469)copy SMILEScopy InChI
Affinity DataEC50:  7.50E+3nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z03979PubMed
TargetCathepsin B(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50391541(CHEMBL2147467)copy SMILEScopy InChI
Affinity DataEC50:  700nMAssay Description:Inhibition of cathepsin B using Z-Phe-Arg-MCA as substrate incubated for 10 mins prior to substrate addition measured after 30 mins by fluorimetric a...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z03979PubMed
TargetProthrombin(Bos taurus (Bovine))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50391540(CHEMBL2147469)copy SMILEScopy InChI
Affinity DataEC50:  2.10E+3nMAssay Description:Inhibition of bovine thrombin using Bz-Phe-Val-Arg-pNA as substrate incubated for 5 mins prior to substrate addition measured after 30 mins by fluori...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z03979PubMed