Compile Data Set for Download or QSAR
Found 110 with Last Name = 'simeon' and Initial = 'c'
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Novartis Pharma AG

Curated by ChEMBL
LigandPNGBDBM50192018(CHEMBL3350037)copy SMILEScopy InChI
Affinity DataKi:  0.501nMAssay Description:Binding affinity for SSTR2 receptors of rat cortex membranes was determined by using [125I][Tyr3]-octreotide radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DB834VPubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Novartis Pharma AG

Curated by ChEMBL
LigandPNGBDBM50215551(CHEMBL410194)copy SMILEScopy InChI
Affinity DataKi:  1.30nMAssay Description:Binding affinity for SSTR2 receptors of rat cortex membranes was determined by using [125I][Tyr3]-octreotide radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DB834VPubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Novartis Pharma AG

Curated by ChEMBL
LigandPNGBDBM50215550(CHEMBL407643)copy SMILEScopy InChI
Affinity DataKi:  3.20nMAssay Description:Binding affinity for SSTR2 receptors of rat cortex membranes was determined by using [125I][Tyr3]-octreotide radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DB834VPubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Novartis Pharma AG

Curated by ChEMBL
LigandPNGBDBM50192018(CHEMBL3350037)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Binding affinity for SSTR2 receptors of rat cortex membranes was determined by using Y-labelled SMT487 radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DB834VPubMed
TargetMitogen-activated protein kinase 15(Homo sapiens (Human))TBA
LigandPNGBDBM50548060(CHEMBL4762609)copy SMILES
Affinity DataIC50: 110nMAssay Description:Inhibition of human ERK8 (2 to 544 residues) incubated for 5 mins in presence of [gamma33P]ATP by scintillation counting analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7MWDPubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50384600(CHEMBL2036792 | US9744172, Compound UNC00000563A)copy SMILEScopy InChI
Affinity DataIC50: 114nMAssay Description:Inhibition of CDK2 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZC867RPubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50384600(CHEMBL2036792 | US9744172, Compound UNC00000563A)copy SMILEScopy InChI
Affinity DataIC50: 199nMAssay Description:Inhibition of CDK4 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZC867RPubMed
TargetGlycylpeptide N-tetradecanoyltransferase 1(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464067(CHEMBL4251359)copy SMILEScopy InChI
Affinity DataIC50: 340nMAssay Description:Inhibition of human NMT1 using [3H]-myristoyl-coA/biotinylated CAP5.5 as substrate after 15 mins by scintillation proximity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetMitogen-activated protein kinase 11(Homo sapiens (Human))TBA
LigandPNGBDBM50548060(CHEMBL4762609)copy SMILES
Affinity DataIC50: 550nMAssay Description:Inhibition of human p38beta MAPK (1 to 364 residues) incubated for 5 mins in presence of [gamma33P]ATP by scintillation counting analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7MWDPubMed
TargetGlycylpeptide N-tetradecanoyltransferase 1(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464069(CHEMBL4237767)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of human NMT1 using [3H]-myristoyl-coA/biotinylated CAP5.5 as substrate after 15 mins by scintillation proximity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464090(CHEMBL4242822)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of human ERG by patch clamp assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464077(CHEMBL4237244)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of human ERG by patch clamp assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464053(CHEMBL4249236)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of human ERG by patch clamp assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464095(CHEMBL4247729)copy SMILEScopy InChI
Affinity DataIC50: 3.10E+3nMAssay Description:Inhibition of human ERG by patch clamp assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464049(CHEMBL4243933)copy SMILEScopy InChI
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibition of human ERG by patch clamp assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464082(CHEMBL4240867)copy SMILEScopy InChI
Affinity DataIC50: 3.70E+3nMAssay Description:Inhibition of human ERG by patch clamp assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50542902(CHEMBL4645906)copy SMILEScopy InChI
Affinity DataIC50: 3.98E+3nMAssay Description:Inhibition of MAOA (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PK0KQ4PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50613723(CHEMBL5268330)copy SMILES
Affinity DataIC50: 5.00E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464085(CHEMBL4243499)copy SMILEScopy InChI
Affinity DataIC50: 5.60E+3nMAssay Description:Inhibition of human ERG by patch clamp assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464054(CHEMBL4246475)copy SMILEScopy InChI
Affinity DataIC50: 6.00E+3nMAssay Description:Inhibition of human ERG by patch clamp assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50613719(CHEMBL5281165)copy SMILES
Affinity DataIC50: 6.00E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50517286(CHEMBL4516798)copy SMILEScopy InChI
Affinity DataIC50: 6.31E+3nMAssay Description:Inhibition of CYP3A4 in human liver microsomes using midazolam as substrate preincubated for 20 mins followed by substrate addition and measured afte...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZC867RPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464048(CHEMBL4250740)copy SMILEScopy InChI
Affinity DataIC50: 6.70E+3nMAssay Description:Inhibition of human ERG by patch clamp assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50613721(CHEMBL5275547)copy SMILES
Affinity DataIC50: 7.00E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetCytochrome P450 1A2(Homo sapiens (Human))TBA
LigandPNGBDBM50613725(CHEMBL5268278)copy SMILES
Affinity DataIC50: 1.00E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetCytochrome P450 2C19(Homo sapiens (Human))TBA
LigandPNGBDBM50613725(CHEMBL5268278)copy SMILES
Affinity DataIC50: 1.00E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetCytochrome P450 2C9(Homo sapiens (Human))TBA
LigandPNGBDBM50613725(CHEMBL5268278)copy SMILES
Affinity DataIC50: 1.00E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetCytochrome P450 2D6(Homo sapiens (Human))TBA
LigandPNGBDBM50613725(CHEMBL5268278)copy SMILES
Affinity DataIC50: 1.00E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50613725(CHEMBL5268278)copy SMILES
Affinity DataIC50: 1.00E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50517286(CHEMBL4516798)copy SMILEScopy InChI
Affinity DataIC50: 1.75E+4nMAssay Description:Inhibition of human ERG by patch clamp assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZC867RPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50613720(CHEMBL5283073)copy SMILES
Affinity DataIC50: 1.80E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50517285(CHEMBL4572962)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of human CDK4 by kinobeads-based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZC867RPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50613716(CHEMBL5283476)copy SMILES
Affinity DataIC50: 2.30E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50613725(CHEMBL5268278)copy SMILES
Affinity DataIC50: 2.40E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50613718(CHEMBL5286709)copy SMILES
Affinity DataIC50: 3.00E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50517287(CHEMBL4563818)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human ERG by patch clamp assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZC867RPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50517285(CHEMBL4572962)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human ERG by patch clamp assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZC867RPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50613726(CHEMBL5272922)copy SMILES
Affinity DataIC50: 3.00E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50613724(CHEMBL5268485)copy SMILES
Affinity DataIC50: 3.60E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetGlycylpeptide N-tetradecanoyltransferase 1(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464096(CHEMBL4241923)copy SMILEScopy InChI
Affinity DataIC50: 3.60E+4nMAssay Description:Inhibition of human NMT1 using [3H]-myristoyl-coA/biotinylated CAP5.5 as substrate after 15 mins by scintillation proximity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50517285(CHEMBL4572962)copy SMILEScopy InChI
Affinity DataIC50: 3.98E+4nMAssay Description:Inhibition of CYP3A4 in human liver microsomes using midazolam as substrate preincubated for 20 mins followed by substrate addition and measured afte...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZC867RPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50517287(CHEMBL4563818)copy SMILEScopy InChI
Affinity DataIC50: 3.98E+4nMAssay Description:Inhibition of CYP3A4 in human liver microsomes using midazolam as substrate preincubated for 20 mins followed by substrate addition and measured afte...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZC867RPubMed
TargetGlycylpeptide N-tetradecanoyltransferase 1(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464062(CHEMBL4248236)copy SMILEScopy InChI
Affinity DataIC50: 4.10E+4nMAssay Description:Inhibition of human NMT1 using [3H]-myristoyl-coA/biotinylated CAP5.5 as substrate after 15 mins by scintillation proximity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetGlycylpeptide N-tetradecanoyltransferase 1(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464073(CHEMBL4250899)copy SMILEScopy InChI
Affinity DataIC50: 4.90E+4nMAssay Description:Inhibition of human NMT1 using [3H]-myristoyl-coA/biotinylated CAP5.5 as substrate after 15 mins by scintillation proximity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetGlycylpeptide N-tetradecanoyltransferase 1(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464094(CHEMBL4245730)copy SMILEScopy InChI
Affinity DataIC50: 6.40E+4nMAssay Description:Inhibition of human NMT1 using [3H]-myristoyl-coA/biotinylated CAP5.5 as substrate after 15 mins by scintillation proximity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetGlycylpeptide N-tetradecanoyltransferase 1(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464080(CHEMBL4249039)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human NMT1 using [3H]-myristoyl-coA/biotinylated CAP5.5 as substrate after 15 mins by scintillation proximity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetGlycylpeptide N-tetradecanoyltransferase 1(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464072(CHEMBL4250444)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human NMT1 using [3H]-myristoyl-coA/biotinylated CAP5.5 as substrate after 15 mins by scintillation proximity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetGlycylpeptide N-tetradecanoyltransferase 1(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464071(CHEMBL4250235)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human NMT1 using [3H]-myristoyl-coA/biotinylated CAP5.5 as substrate after 15 mins by scintillation proximity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetGlycylpeptide N-tetradecanoyltransferase 1(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464070(CHEMBL4247869)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human NMT1 using [3H]-myristoyl-coA/biotinylated CAP5.5 as substrate after 15 mins by scintillation proximity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
TargetGlycylpeptide N-tetradecanoyltransferase 1(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50464068(CHEMBL4240800)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human NMT1 using [3H]-myristoyl-coA/biotinylated CAP5.5 as substrate after 15 mins by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7CR1PubMed
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