BDBM50625771 CHEMBL5397768
SMILES CN1CC(=O)N[C@@H](CO)C(=O)N[C@@H](Cc2ccc(cc2)-c2ccccc2)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(=O)N[C@@H](CSCC(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](Cc2ccc(O)cc2)C1=O)C(=O)NCC(N)=O
InChI Key InChIKey=CTCKWRVXWBIVLC-UHFFFAOYSA-N
Data 2 Kd
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 50625771
TargetInactive tyrosine-protein kinase transmembrane receptor ROR1(Homo sapiens)
Princeton University
Curated by ChEMBL
Princeton University
Curated by ChEMBL
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 InfoSimilars
TargetTyrosine-protein kinase transmembrane receptor ROR2(Homo sapiens)
Princeton University
Curated by ChEMBL
Princeton University
Curated by ChEMBL
Affinity DataKd: >100nMAssay 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
