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SMILES: CC1CCC(C)N1CCCOc1cccc(c1C)-c1cccc2[C@H](CCc12)Oc1cc(OCc2cc(cc(c2)C#N)C#N)c(CN[C@H]2CCC(=O)NC2)cc1Cl

InChI Key: InChIKey=MBVAGARUTDXBQO-KVHSLDQSSA-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 = 482605   
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))
BDBM482605
PNG
(US10919852, Compound TABLE 1.304 | US11708326, Com...)
Show SMILES CC1CCC(C)N1CCCOc1cccc(c1C)-c1cccc2[C@H](CCc12)Oc1cc(OCc2cc(cc(c2)C#N)C#N)c(CN[C@H]2CCC(=O)NC2)cc1Cl |r|
Show InChI InChI=1S/C46H50ClN5O4/c1-29-11-12-30(2)52(29)17-6-18-54-42-10-5-7-37(31(42)3)38-8-4-9-40-39(38)14-15-43(40)56-45-23-44(55-28-34-20-32(24-48)19-33(21-34)25-49)35(22-41(45)47)26-50-36-13-16-46(53)51-27-36/h4-5,7-10,19-23,29-30,36,43,50H,6,11-18,26-28H2,1-3H3,(H,51,53)/t29?,30?,36-,43-/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)
BDBM482605
PNG
(US10919852, Compound TABLE 1.304 | US11708326, Com...)
Show SMILES CC1CCC(C)N1CCCOc1cccc(c1C)-c1cccc2[C@H](CCc12)Oc1cc(OCc2cc(cc(c2)C#N)C#N)c(CN[C@H]2CCC(=O)NC2)cc1Cl |r|
Show InChI InChI=1S/C46H50ClN5O4/c1-29-11-12-30(2)52(29)17-6-18-54-42-10-5-7-37(31(42)3)38-8-4-9-40-39(38)14-15-43(40)56-45-23-44(55-28-34-20-32(24-48)19-33(21-34)25-49)35(22-41(45)47)26-50-36-13-16-46(53)51-27-36/h4-5,7-10,19-23,29-30,36,43,50H,6,11-18,26-28H2,1-3H3,(H,51,53)/t29?,30?,36-,43-/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