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SMILES: COc1ccccc1-c1oc2ncnc(N[C@H](CO)c3ccccc3)c2c1-c1cccc(NC(=O)C=C)c1

InChI Key: InChIKey=PDGXQCBYLSUPPW-HSZRJFAPSA-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 8 hits for monomerid = 50530618   
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
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50530618
PNG
(CHEMBL4559807)
Show SMILES COc1ccccc1-c1oc2ncnc(N[C@H](CO)c3ccccc3)c2c1-c1cccc(NC(=O)C=C)c1 |r|
Show InChI InChI=1S/C30H26N4O4/c1-3-25(36)33-21-13-9-12-20(16-21)26-27-29(34-23(17-35)19-10-5-4-6-11-19)31-18-32-30(27)38-28(26)22-14-7-8-15-24(22)37-2/h3-16,18,23,35H,1,17H2,2H3,(H,33,36)(H,31,32,34)/t23-/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
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PC cid
PC sid
UniChem
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PubMed
n/an/a 24n/an/an/an/an/an/a



National Health Research Institutes

Curated by ChEMBL


Assay Description
Inhibition of GST-tagged human EGFR kinase domain (696 to 1022 residues) using poly(Glu, Tyr) 4:1 substrate incubated for 60 mins by kinase-Glo plus ...


J Med Chem 62: 10108-10123 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00722
BindingDB Entry DOI: 10.7270/Q21V5JFW
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50530618
PNG
(CHEMBL4559807)
Show SMILES COc1ccccc1-c1oc2ncnc(N[C@H](CO)c3ccccc3)c2c1-c1cccc(NC(=O)C=C)c1 |r|
Show InChI InChI=1S/C30H26N4O4/c1-3-25(36)33-21-13-9-12-20(16-21)26-27-29(34-23(17-35)19-10-5-4-6-11-19)31-18-32-30(27)38-28(26)22-14-7-8-15-24(22)37-2/h3-16,18,23,35H,1,17H2,2H3,(H,33,36)(H,31,32,34)/t23-/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 24n/an/an/an/an/an/a



National Health Research Institutes

Curated by ChEMBL


Assay Description
Inhibition of GST-tagged human EGFR kinase domain (696 to 1022 residues) using poly(Glu, Tyr) 4:1 substrate incubated for 60 mins by kinase-Glo plus ...


J Med Chem 62: 10108-10123 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00722
BindingDB Entry DOI: 10.7270/Q21V5JFW
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50530618
PNG
(CHEMBL4559807)
Show SMILES COc1ccccc1-c1oc2ncnc(N[C@H](CO)c3ccccc3)c2c1-c1cccc(NC(=O)C=C)c1 |r|
Show InChI InChI=1S/C30H26N4O4/c1-3-25(36)33-21-13-9-12-20(16-21)26-27-29(34-23(17-35)19-10-5-4-6-11-19)31-18-32-30(27)38-28(26)22-14-7-8-15-24(22)37-2/h3-16,18,23,35H,1,17H2,2H3,(H,33,36)(H,31,32,34)/t23-/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 157n/an/an/an/an/an/a



National Health Research Institutes

Curated by ChEMBL


Assay Description
Inhibition of GST-tagged human EGFR kinase domain I858R/T790M mutant (696 to 1022 residues) using EGFR L858R/T790M substrate peptide incubated for 12...


J Med Chem 62: 10108-10123 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00722
BindingDB Entry DOI: 10.7270/Q21V5JFW
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50530618
PNG
(CHEMBL4559807)
Show SMILES COc1ccccc1-c1oc2ncnc(N[C@H](CO)c3ccccc3)c2c1-c1cccc(NC(=O)C=C)c1 |r|
Show InChI InChI=1S/C30H26N4O4/c1-3-25(36)33-21-13-9-12-20(16-21)26-27-29(34-23(17-35)19-10-5-4-6-11-19)31-18-32-30(27)38-28(26)22-14-7-8-15-24(22)37-2/h3-16,18,23,35H,1,17H2,2H3,(H,33,36)(H,31,32,34)/t23-/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 157n/an/an/an/an/an/a



National Health Research Institutes

Curated by ChEMBL


Assay Description
Inhibition of GST-tagged human EGFR kinase domain I858R/T790M mutant (696 to 1022 residues) using EGFR L858R/T790M substrate peptide incubated for 12...


J Med Chem 62: 10108-10123 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00722
BindingDB Entry DOI: 10.7270/Q21V5JFW
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50530618
PNG
(CHEMBL4559807)
Show SMILES COc1ccccc1-c1oc2ncnc(N[C@H](CO)c3ccccc3)c2c1-c1cccc(NC(=O)C=C)c1 |r|
Show InChI InChI=1S/C30H26N4O4/c1-3-25(36)33-21-13-9-12-20(16-21)26-27-29(34-23(17-35)19-10-5-4-6-11-19)31-18-32-30(27)38-28(26)22-14-7-8-15-24(22)37-2/h3-16,18,23,35H,1,17H2,2H3,(H,33,36)(H,31,32,34)/t23-/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 0.145n/an/an/an/an/an/a



National Health Research Institutes

Curated by ChEMBL


Assay Description
Inhibition of GST-tagged human EGFR A763_Y764insFHEA mutant using poly(Glu, Tyr) 4:1 substrate incubated for 120 mins by kinase-Glo plus luminescent ...


J Med Chem 62: 10108-10123 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00722
BindingDB Entry DOI: 10.7270/Q21V5JFW
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50530618
PNG
(CHEMBL4559807)
Show SMILES COc1ccccc1-c1oc2ncnc(N[C@H](CO)c3ccccc3)c2c1-c1cccc(NC(=O)C=C)c1 |r|
Show InChI InChI=1S/C30H26N4O4/c1-3-25(36)33-21-13-9-12-20(16-21)26-27-29(34-23(17-35)19-10-5-4-6-11-19)31-18-32-30(27)38-28(26)22-14-7-8-15-24(22)37-2/h3-16,18,23,35H,1,17H2,2H3,(H,33,36)(H,31,32,34)/t23-/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 0.636n/an/an/an/an/an/a



National Health Research Institutes

Curated by ChEMBL


Assay Description
Inhibition of GST-tagged human EGFR D770_N771insNPG mutant using poly(Glu, Tyr) 4:1 substrate incubated for 120 mins by kinase-Glo plus luminescent k...


J Med Chem 62: 10108-10123 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00722
BindingDB Entry DOI: 10.7270/Q21V5JFW
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50530618
PNG
(CHEMBL4559807)
Show SMILES COc1ccccc1-c1oc2ncnc(N[C@H](CO)c3ccccc3)c2c1-c1cccc(NC(=O)C=C)c1 |r|
Show InChI InChI=1S/C30H26N4O4/c1-3-25(36)33-21-13-9-12-20(16-21)26-27-29(34-23(17-35)19-10-5-4-6-11-19)31-18-32-30(27)38-28(26)22-14-7-8-15-24(22)37-2/h3-16,18,23,35H,1,17H2,2H3,(H,33,36)(H,31,32,34)/t23-/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 0.145n/an/an/an/an/an/a



National Health Research Institutes

Curated by ChEMBL


Assay Description
Inhibition of GST-tagged human EGFR A763_Y764insFHEA mutant using poly(Glu, Tyr) 4:1 substrate incubated for 120 mins by kinase-Glo plus luminescent ...


J Med Chem 62: 10108-10123 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00722
BindingDB Entry DOI: 10.7270/Q21V5JFW
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50530618
PNG
(CHEMBL4559807)
Show SMILES COc1ccccc1-c1oc2ncnc(N[C@H](CO)c3ccccc3)c2c1-c1cccc(NC(=O)C=C)c1 |r|
Show InChI InChI=1S/C30H26N4O4/c1-3-25(36)33-21-13-9-12-20(16-21)26-27-29(34-23(17-35)19-10-5-4-6-11-19)31-18-32-30(27)38-28(26)22-14-7-8-15-24(22)37-2/h3-16,18,23,35H,1,17H2,2H3,(H,33,36)(H,31,32,34)/t23-/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 0.636n/an/an/an/an/an/a



National Health Research Institutes

Curated by ChEMBL


Assay Description
Inhibition of GST-tagged human EGFR D770_N771insNPG mutant using poly(Glu, Tyr) 4:1 substrate incubated for 120 mins by kinase-Glo plus luminescent k...


J Med Chem 62: 10108-10123 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00722
BindingDB Entry DOI: 10.7270/Q21V5JFW
More data for this
Ligand-Target Pair