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BDBM50384916 CHEMBL2036504

SMILES: CCOC(=O)c1c(C)nc2ccccc2c1SCCC#N

InChI Key: InChIKey=MISVWQNQFNWNCR-UHFFFAOYSA-N

Data: 2 KI

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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50384916   
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
Myristoyl-CoA:protein N-myristoyltransferase (Nmt)


(Homo sapiens (Human))
BDBM50384916
PNG
(CHEMBL2036504)
Show SMILES CCOC(=O)c1c(C)nc2ccccc2c1SCCC#N
Show InChI InChI=1S/C16H16N2O2S/c1-3-20-16(19)14-11(2)18-13-8-5-4-7-12(13)15(14)21-10-6-9-17/h4-5,7-8H,3,6,10H2,1-2H3
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MMDB

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PC cid
PC sid
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Similars

Article
PubMed
1.08E+4n/an/an/an/an/an/an/an/a



Imperial College London

Curated by ChEMBL


Assay Description
Inhibition of human N-myristoyltransferase 1 using human pp60Src92-16 amino acids) as substrate


J Med Chem 55: 3578-82 (2012)


Article DOI: 10.1021/jm300040p
BindingDB Entry DOI: 10.7270/Q2BC40KN
More data for this
Ligand-Target Pair
Peptide N-myristoyltransferase 2


(Homo sapiens (Human))
BDBM50384916
PNG
(CHEMBL2036504)
Show SMILES CCOC(=O)c1c(C)nc2ccccc2c1SCCC#N
Show InChI InChI=1S/C16H16N2O2S/c1-3-20-16(19)14-11(2)18-13-8-5-4-7-12(13)15(14)21-10-6-9-17/h4-5,7-8H,3,6,10H2,1-2H3
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
4.15E+4n/an/an/an/an/an/an/an/a



Imperial College London

Curated by ChEMBL


Assay Description
Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrate


J Med Chem 55: 3578-82 (2012)


Article DOI: 10.1021/jm300040p
BindingDB Entry DOI: 10.7270/Q2BC40KN
More data for this
Ligand-Target Pair