Reaction Details Report a problem with these data
Target
Programmed cell death 1 ligand 1
Ligand
BDBM365921
Substrate
n/a
Meas. Tech.
Homogenous Time-Resolved Fluorescence (HTRF) Binding Assay
IC50
53±n/a nM
Citation
 Chupak, LS; Zheng, X Compounds useful as immunomodulators US Patent  US9872852 Publication Date 1/23/2018 
Target
Name:
Programmed cell death 1 ligand 1
Synonyms:
B7 homolog 1 | B7-H1 | B7H1 | B7H1 | CD274 | CD_antigen=CD274 | PD-L1 | PD1L1_HUMAN | PDCD1 ligand 1 | PDCD1L1 | PDCD1LG1 | PDL1 | Programmed cell death 1 ligand 1 | Programmed death ligand 1
Type:
PROTEIN
Mol. Mass.:
33278.49
Organism:
Homo sapiens (Human)
Description:
ChEMBL_109807
Residue:
290
Sequence:
MRIFAVFIFMTYWHLLNAFTVTVPKDLYVVEYGSNMTIECKFPVEKQLDLAALIVYWEMEDKNIIQFVHGEEDLKVQHSSYRQRARLLKDQLSLGNAALQITDVKLQDAGVYRCMISYGGADYKRITVKVNAPYNKINQRILVVDPVTSEHELTCQAEGYPKAEVIWTSSDHQVLSGKTTTTNSKREEKLFNVTSTLRINTTTNEIFYCTFRRLDPEENHTAELVIPELPLAHPPNERTHLVILGAILLCLGVALTFIFRLRKGRMMDVKKCGIQDTNSKKQSDTHLEET
  
Inhibitor
Name:
BDBM365921
Synonyms:
({2,6-dimethoxy-4-[(2-methyl-3- phenylphenyl)methoxy]phenyl} methyl)[3-(1H-imidazol-1- yl)propyl]amine | US9872852, Example 173
Type:
Small organic molecule
Emp. Form.:
C29H33N3O3
Mol. Mass.:
471.5906
SMILES:
COc1cc(OCc2cccc(c2C)-c2ccccc2)cc(OC)c1CNCCCn1ccnc1
Structure:
Search PDB for entries with ligand similarity: