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BDBM4355 (2E)-2-cyano-3-(4-hydroxyphenyl)prop-2-enamide::CHEMBL308048::benzylidenemalononitrile (BMN) deriv. 39

SMILES: NC(=O)C(=C\c1ccc(O)cc1)\C#N

InChI Key: InChIKey=ILLYSIXRHPOKIQ-VMPITWQZSA-N

Data: 1 KI  3 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 4355   
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
Prothrombin


(Homo sapiens (Human))
BDBM4355
PNG
((2E)-2-cyano-3-(4-hydroxyphenyl)prop-2-enamide | C...)
Show SMILES NC(=O)C(=C\c1ccc(O)cc1)\C#N
Show InChI InChI=1S/C10H8N2O2/c11-6-8(10(12)14)5-7-1-3-9(13)4-2-7/h1-5,13H,(H2,12,14)/b8-5+
PDB

UniProtKB/SwissProt

antibodypedia
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CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
1.02E+5n/an/an/an/an/an/an/an/a



University of Heidelberg

Curated by ChEMBL


Assay Description
Inhibition of human thrombin using Boc-VPR-AMC as substrate compound preincubated for 15 mins before substrate addition measured up to 10 mins by spe...


Bioorg Med Chem 19: 7318-37 (2011)


Article DOI: 10.1016/j.bmc.2011.10.061
BindingDB Entry DOI: 10.7270/Q2474B8H
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM4355
PNG
((2E)-2-cyano-3-(4-hydroxyphenyl)prop-2-enamide | C...)
Show SMILES NC(=O)C(=C\c1ccc(O)cc1)\C#N
Show InChI InChI=1S/C10H8N2O2/c11-6-8(10(12)14)5-7-1-3-9(13)4-2-7/h1-5,13H,(H2,12,14)/b8-5+
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
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CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 8n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of EGFR in human A431 cells


J Nat Prod 55: 1529-1560 (1992)


Article DOI: 10.1021/np50089a001
BindingDB Entry DOI: 10.7270/Q2J966CC
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM4355
PNG
((2E)-2-cyano-3-(4-hydroxyphenyl)prop-2-enamide | C...)
Show SMILES NC(=O)C(=C\c1ccc(O)cc1)\C#N
Show InChI InChI=1S/C10H8N2O2/c11-6-8(10(12)14)5-7-1-3-9(13)4-2-7/h1-5,13H,(H2,12,14)/b8-5+
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 8.00E+5n/an/an/an/an/an/a



Hebrew University of Jerusalem



Assay Description
The activity of EGFR, preactivated with EGF, is measured by its ability to transfer terminal phosphate from [gamma-32P]ATP to poly(GAT) substrate.


J Med Chem 32: 2344-52 (1989)


Article DOI: 10.1021/jm00130a020
BindingDB Entry DOI: 10.7270/Q2G44NHF
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM4355
PNG
((2E)-2-cyano-3-(4-hydroxyphenyl)prop-2-enamide | C...)
Show SMILES NC(=O)C(=C\c1ccc(O)cc1)\C#N
Show InChI InChI=1S/C10H8N2O2/c11-6-8(10(12)14)5-7-1-3-9(13)4-2-7/h1-5,13H,(H2,12,14)/b8-5+
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 1.00E+6n/an/an/an/an/an/a



National Cancer Institute

Curated by ChEMBL


Assay Description
Ability to inhibit autophosphorylation of immunopurified p56Ick


J Med Chem 36: 425-32 (1993)


BindingDB Entry DOI: 10.7270/Q2CV4GTQ
More data for this
Ligand-Target Pair