Compile Data Set for Download or QSAR
Found 33 with Last Name = 'peterson' and Initial = 'jm'
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449332(CHEMBL3126041)copy SMILEScopy InChI
Affinity DataKi:  2nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449331(CHEMBL3126043)copy SMILEScopy InChI
Affinity DataKi:  3nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449330(CHEMBL3126045)copy SMILEScopy InChI
Affinity DataKi:  4nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449329(CHEMBL3126046)copy SMILEScopy InChI
Affinity DataKi:  5nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449328(CHEMBL3126047)copy SMILEScopy InChI
Affinity DataKi:  5nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449327(CHEMBL3126039)copy SMILEScopy InChI
Affinity DataKi:  5nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449326(CHEMBL3126040)copy SMILEScopy InChI
Affinity DataKi:  6nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449325(CHEMBL3126044)copy SMILEScopy InChI
Affinity DataKi:  7nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449323(CHEMBL3126053)copy SMILEScopy InChI
Affinity DataKi:  8nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449324(CHEMBL3126042)copy SMILEScopy InChI
Affinity DataKi:  8nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449321(CHEMBL3126052)copy SMILEScopy InChI
Affinity DataKi:  9nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449322(CHEMBL3126048)copy SMILEScopy InChI
Affinity DataKi:  9nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449320(CHEMBL3126050)copy SMILEScopy InChI
Affinity DataKi:  10nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449319(CHEMBL3126049)copy SMILEScopy InChI
Affinity DataKi:  12nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449318(CHEMBL3126051)copy SMILEScopy InChI
Affinity DataKi:  41nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449317(CHEMBL3126054)copy SMILEScopy InChI
Affinity DataKi:  720nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lundbeck Research USA, Inc.

Curated by ChEMBL
LigandPNGBDBM50449316(CHEMBL3126038)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [125I]PYY from human NPY5 receptor transfected in LM(tk-) cell membranes after 120 mins by solid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HT1PubMed
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528667(US11197877, Compound 43)copy SMILES
Affinity DataIC50: 106nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528668(US11197877, Compound 44)copy SMILES
Affinity DataIC50: 136nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528653(US11197877, Compound 17)copy SMILES
Affinity DataIC50: 150nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528655(US11197877, Compound 18)copy SMILES
Affinity DataIC50: 170nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528656(US11197877, Compound 24)copy SMILES
Affinity DataIC50: 190nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528669(US11197877, Compound 46)copy SMILES
Affinity DataIC50: 192nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528659(US11197877, Compound 20)copy SMILES
Affinity DataIC50: 240nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528664(US11197877, Compound 34)copy SMILES
Affinity DataIC50: 340nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528665(US11197877, Compound 36)copy SMILES
Affinity DataIC50: 510nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528660(US11197877, Compound 21)copy SMILES
Affinity DataIC50: 520nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528658(US11197877, Compound 19)copy SMILES
Affinity DataIC50: 580nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528657(US11197877, Compound 25)copy SMILES
Affinity DataIC50: 660nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528666(US11197877, Compound 35)copy SMILES
Affinity DataIC50: 720nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528663(US11197877, Compound 33)copy SMILES
Affinity DataIC50: 2.12E+3nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528662(US11197877, Compound 31)copy SMILES
Affinity DataIC50: 2.36E+3nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent
TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528661(US11197877, Compound 30)copy SMILES
Affinity DataIC50: 2.78E+3nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent