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SMILES: COc1cc(N(C)CCN(C)C)c(NC(=O)C=C)cc1Nc1nc(C)cc(n1)-c1cn(C)c2ccccc12

InChI Key: InChIKey=MFMJUEMNPKCWHW-UHFFFAOYSA-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 4 hits for monomerid = 50529689   
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))
BDBM50529689
PNG
(CHEMBL4557005)
Show SMILES COc1cc(N(C)CCN(C)C)c(NC(=O)C=C)cc1Nc1nc(C)cc(n1)-c1cn(C)c2ccccc12
Show InChI InChI=1S/C29H35N7O2/c1-8-28(37)31-23-16-24(27(38-7)17-26(23)35(5)14-13-34(3)4)33-29-30-19(2)15-22(32-29)21-18-36(6)25-12-10-9-11-20(21)25/h8-12,15-18H,1,13-14H2,2-7H3,(H,31,37)(H,30,32,33)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 93n/an/an/an/an/an/a



Jiangxi Science & Technology Normal University

Curated by ChEMBL


Assay Description
Inhibition of EGFR T790M/L858R double mutant (unknown origin) using substrate-biotin by ELISA-based mobility shift assay


Eur J Med Chem 163: 367-380 (2019)


Article DOI: 10.1016/j.ejmech.2018.11.069
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50529689
PNG
(CHEMBL4557005)
Show SMILES COc1cc(N(C)CCN(C)C)c(NC(=O)C=C)cc1Nc1nc(C)cc(n1)-c1cn(C)c2ccccc12
Show InChI InChI=1S/C29H35N7O2/c1-8-28(37)31-23-16-24(27(38-7)17-26(23)35(5)14-13-34(3)4)33-29-30-19(2)15-22(32-29)21-18-36(6)25-12-10-9-11-20(21)25/h8-12,15-18H,1,13-14H2,2-7H3,(H,31,37)(H,30,32,33)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 1.34E+3n/an/an/an/an/an/a



Jiangxi Science & Technology Normal University

Curated by ChEMBL


Assay Description
Inhibition of wild-type EGFR (unknown origin) using substrate-biotin by ELISA-based mobility shift assay


Eur J Med Chem 163: 367-380 (2019)


Article DOI: 10.1016/j.ejmech.2018.11.069
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50529689
PNG
(CHEMBL4557005)
Show SMILES COc1cc(N(C)CCN(C)C)c(NC(=O)C=C)cc1Nc1nc(C)cc(n1)-c1cn(C)c2ccccc12
Show InChI InChI=1S/C29H35N7O2/c1-8-28(37)31-23-16-24(27(38-7)17-26(23)35(5)14-13-34(3)4)33-29-30-19(2)15-22(32-29)21-18-36(6)25-12-10-9-11-20(21)25/h8-12,15-18H,1,13-14H2,2-7H3,(H,31,37)(H,30,32,33)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 93n/an/an/an/an/an/a



Jiangxi Science & Technology Normal University

Curated by ChEMBL


Assay Description
Inhibition of EGFR T790M/L858R double mutant (unknown origin) using substrate-biotin by ELISA-based mobility shift assay


Eur J Med Chem 163: 367-380 (2019)


Article DOI: 10.1016/j.ejmech.2018.11.069
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50529689
PNG
(CHEMBL4557005)
Show SMILES COc1cc(N(C)CCN(C)C)c(NC(=O)C=C)cc1Nc1nc(C)cc(n1)-c1cn(C)c2ccccc12
Show InChI InChI=1S/C29H35N7O2/c1-8-28(37)31-23-16-24(27(38-7)17-26(23)35(5)14-13-34(3)4)33-29-30-19(2)15-22(32-29)21-18-36(6)25-12-10-9-11-20(21)25/h8-12,15-18H,1,13-14H2,2-7H3,(H,31,37)(H,30,32,33)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 1.34E+3n/an/an/an/an/an/a



Jiangxi Science & Technology Normal University

Curated by ChEMBL


Assay Description
Inhibition of wild-type EGFR (unknown origin) using substrate-biotin by ELISA-based mobility shift assay


Eur J Med Chem 163: 367-380 (2019)


Article DOI: 10.1016/j.ejmech.2018.11.069
More data for this
Ligand-Target Pair