BindingDB logo
myBDB logout

null

SMILES: O[C@H]1CCC[C@@H]1NCc1cc(Cl)c(O[C@H]2CCc3c2cccc3-c2cccc(OCCCN3CC4(C3)CC(F)(F)C4)c2Cl)cc1OCc1cncc(c1)C#N

InChI Key: InChIKey=YBFJIKBTCKTWAG-FSEITFBQSA-N

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 482546   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Programmed cell death 1 ligand 1


(Homo sapiens (Human))
BDBM482546
PNG
(US10919852, Compound TABLE 1.245 | US11708326, Com...)
Show SMILES O[C@H]1CCC[C@@H]1NCc1cc(Cl)c(O[C@H]2CCc3c2cccc3-c2cccc(OCCCN3CC4(C3)CC(F)(F)C4)c2Cl)cc1OCc1cncc(c1)C#N |r|
Show InChI InChI=1S/C43H44Cl2F2N4O4/c44-34-16-29(21-50-35-8-3-9-36(35)52)39(54-22-28-15-27(18-48)19-49-20-28)17-40(34)55-37-12-11-31-30(5-1-6-32(31)37)33-7-2-10-38(41(33)45)53-14-4-13-51-25-42(26-51)23-43(46,47)24-42/h1-2,5-7,10,15-17,19-20,35-37,50,52H,3-4,8-9,11-14,21-26H2/t35-,36-,37-/m0/s1
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/a<5n/an/an/an/an/an/a


TBA



Citation and Details

BindingDB Entry DOI: 10.7270/Q22N56DJ
More data for this
Ligand-Target Pair
Programmed cell death protein 1


(Homo sapiens)
BDBM482546
PNG
(US10919852, Compound TABLE 1.245 | US11708326, Com...)
Show SMILES O[C@H]1CCC[C@@H]1NCc1cc(Cl)c(O[C@H]2CCc3c2cccc3-c2cccc(OCCCN3CC4(C3)CC(F)(F)C4)c2Cl)cc1OCc1cncc(c1)C#N |r|
Show InChI InChI=1S/C43H44Cl2F2N4O4/c44-34-16-29(21-50-35-8-3-9-36(35)52)39(54-22-28-15-27(18-48)19-49-20-28)17-40(34)55-37-12-11-31-30(5-1-6-32(31)37)33-7-2-10-38(41(33)45)53-14-4-13-51-25-42(26-51)23-43(46,47)24-42/h1-2,5-7,10,15-17,19-20,35-37,50,52H,3-4,8-9,11-14,21-26H2/t35-,36-,37-/m0/s1
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a<5n/an/an/an/an/an/a



ChemoCentryx, Inc.

US Patent


Assay Description
96 Well plates were coated with 1 g/mL of human PD-L1 (obtained from R&D) in PBS overnight at 4° C. The wells were then blocked with 2% BSA in PBS (W...


US Patent US10919852 (2021)


BindingDB Entry DOI: 10.7270/Q2RF5Z3R
More data for this
Ligand-Target Pair