Compile Data Set for Download or QSAR
Report error Found 17 of affinity data for UniProtKB/TrEMBL: Q01973
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625771(CHEMBL5397768)
Affinity DataKd:  3nMAssay Description:Binding affinity to full length human His-tagged ROR1 (937 residues ) assessed as dissociation constant by SPR analysisMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625772(CHEMBL5411958)
Affinity DataKd:  22nMAssay Description:Binding affinity to full length human His-tagged ROR1 (937 residues ) assessed as dissociation constant by SPR analysisMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625773(CHEMBL5415252)
Affinity DataKd:  34nMAssay Description:Binding affinity to full length human His-tagged ROR1 (937 residues ) assessed as dissociation constant by SPR analysisMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625770(CHEMBL5416192)
Affinity DataKd:  11nMAssay Description:Binding affinity to full length human His-tagged ROR1 (937 residues ) assessed as dissociation constant by SPR analysisMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625784(CHEMBL5428267)
Affinity DataIC50: 2.20nMAssay Description:Binding affinity to human ROR1 expressed in HEK293 cells by cell based assayMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625783(CHEMBL5399065)
Affinity DataIC50: 5.20nMAssay Description:Binding affinity to human ROR1 expressed in HEK293 cells by cell based assayMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625782(CHEMBL5397895)
Affinity DataIC50: 5.30nMAssay Description:Binding affinity to human ROR1 expressed in HEK293 cells by cell based assayMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625781(CHEMBL5427174)
Affinity DataIC50: 6.30nMAssay Description:Binding affinity to human ROR1 expressed in HEK293 cells by cell based assayMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625779(CHEMBL5437151)
Affinity DataIC50: 7.20nMAssay Description:Binding affinity to human ROR1 expressed in HEK293 cells by cell based assayMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625780(CHEMBL5408107)
Affinity DataIC50: 7.20nMAssay Description:Binding affinity to human ROR1 expressed in HEK293 cells by cell based assayMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625778(CHEMBL5410563)
Affinity DataIC50: 8.60nMAssay Description:Binding affinity to human ROR1 expressed in HEK293 cells by cell based assayMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625777(CHEMBL5424562)
Affinity DataIC50: 9.90nMAssay Description:Binding affinity to human ROR1 expressed in HEK293 cells by cell based assayMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625776(CHEMBL5396415)
Affinity DataIC50: 10nMAssay Description:Binding affinity to human ROR1 expressed in HEK293 cells by cell based assayMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625775(CHEMBL5422581)
Affinity DataIC50: 12nMAssay Description:Binding affinity to human ROR1 expressed in HEK293 cells by cell based assayMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625770(CHEMBL5416192)
Affinity DataIC50: 13nMAssay Description:Binding affinity to human ROR1 expressed in HEK293 cells by cell based assayMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625774(CHEMBL5427967)
Affinity DataIC50: 14nMAssay Description:Binding affinity to human ROR1 expressed in HEK293 cells by cell based assayMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University

Curated by ChEMBL
LigandPNGBDBM50625772(CHEMBL5411958)
Affinity DataIC50: 66nMAssay Description:Binding affinity to ROR1 (unknown origin)More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
PubMed