BDBM50525146 CHEMBL4462272
SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H]1CSSC[C@H](NC(=O)[C@H](CS)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](CS)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC1=O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O
InChI Key InChIKey=DYVWVNCGFIBINN-UHFFFAOYSA-N
Data 2 Kd
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 50525146
TargetTumor necrosis factor ligand superfamily member 11(Human)
Shanghai Jiaotong University School of Medicine
Curated by ChEMBL
Shanghai Jiaotong University School of Medicine
Curated by ChEMBL
Affinity DataKd: 1.73E+4nMAssay Description:Binding affinity to human RANKL by surface plasmon resonance analysisMore data for this Ligand-Target Pair
TargetTumor necrosis factor ligand superfamily member 11(Mouse)
Shanghai Jiaotong University School of Medicine
Curated by ChEMBL
Shanghai Jiaotong University School of Medicine
Curated by ChEMBL
Affinity DataKd: 1.73E+4nMAssay Description:Binding affinity to mouse N-terminal His6-Trx-tagged RANKL ectodomain (157 to 316 residues) expressed in Escherichia coli BL21 (DE3) by isothermal ti...More data for this Ligand-Target Pair