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SMILES: Cc1c(OCCCN2CCCCC2)cccc1-c1cccc2[C@H](CCc12)Oc1cc(OCc2cncc(c2)C#N)c(CNC[C@@H]2CCC(=O)N2)cc1Cl

InChI Key: InChIKey=FHGZZFPLNXNVGT-QQLMSYFVSA-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 = 482569   
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))
BDBM482569
PNG
(US10919852, Compound TABLE 1.268 | US11708326, Com...)
Show SMILES Cc1c(OCCCN2CCCCC2)cccc1-c1cccc2[C@H](CCc12)Oc1cc(OCc2cncc(c2)C#N)c(CNC[C@@H]2CCC(=O)N2)cc1Cl |r|
Show InChI InChI=1S/C43H48ClN5O4/c1-29-34(8-6-11-39(29)51-19-7-18-49-16-3-2-4-17-49)35-9-5-10-37-36(35)13-14-40(37)53-42-22-41(52-28-31-20-30(23-45)24-46-25-31)32(21-38(42)44)26-47-27-33-12-15-43(50)48-33/h5-6,8-11,20-22,24-25,33,40,47H,2-4,7,12-19,26-28H2,1H3,(H,48,50)/t33-,40-/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)
BDBM482569
PNG
(US10919852, Compound TABLE 1.268 | US11708326, Com...)
Show SMILES Cc1c(OCCCN2CCCCC2)cccc1-c1cccc2[C@H](CCc12)Oc1cc(OCc2cncc(c2)C#N)c(CNC[C@@H]2CCC(=O)N2)cc1Cl |r|
Show InChI InChI=1S/C43H48ClN5O4/c1-29-34(8-6-11-39(29)51-19-7-18-49-16-3-2-4-17-49)35-9-5-10-37-36(35)13-14-40(37)53-42-22-41(52-28-31-20-30(23-45)24-46-25-31)32(21-38(42)44)26-47-27-33-12-15-43(50)48-33/h5-6,8-11,20-22,24-25,33,40,47H,2-4,7,12-19,26-28H2,1H3,(H,48,50)/t33-,40-/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