BDBM50625770 CHEMBL5416192
SMILES CC(C)C[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2ccccc2)NC(=O)CSC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccccc2)N(C)C(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H](NC1=O)C(C)C)C(=O)NCC(N)=O
InChI Key InChIKey=ILLCRYUBFFYODW-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 50625770
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University
Curated by ChEMBL
Princeton University
Curated by ChEMBL
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 InfoSimilars
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University
Curated by ChEMBL
Princeton University
Curated by ChEMBL
Affinity DataIC50: 13nMAssay Description:Binding affinity to human ROR1 expressed in HEK293 cells by cell based assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
TargetTyrosine-protein kinase transmembrane receptor ROR2(Homo sapiens)
Princeton University
Curated by ChEMBL
Princeton University
Curated by ChEMBL
Affinity DataKd: 43nMAssay Description:Binding affinity to full length human His-tagged ROR2 (943 residues ) assessed as dissociation constant by SPR analysisMore data for this Ligand-Target Pair
Ligand InfoSimilars
