BDBM50218688 CHEMBL416300

SMILES CCOC(=O)c1oc2cccc(OCCCNC(C)C)c2c1C

InChI Key InChIKey=AOKNIRNUINXDSR-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50218688   

TargetBeta-1/Beta-2/Beta-3 adrenergic receptor(Human)
Nippon Roche Research Center

Curated by ChEMBL
LigandPNGBDBM50218688(CHEMBL416300)
Affinity DataIC50: 3.80E+4nMAssay Description:Compound was evaluated for its Beta adrenergic receptor blocking actionMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2018
Entry Details Article
PubMed
TargetGlycylpeptide N-tetradecanoyltransferase 1/2(Human)
Nippon Roche Research Center

Curated by ChEMBL
LigandPNGBDBM50218688(CHEMBL416300)
Affinity DataIC50: 3.80E+5nMAssay Description:Inhibitory activity against human N-myristoyltransferase (HsNmt)More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2018
Entry Details Article
PubMed
TargetGlycylpeptide N-tetradecanoyltransferase 1/2(Human)
Nippon Roche Research Center

Curated by ChEMBL
LigandPNGBDBM50218688(CHEMBL416300)
Affinity DataIC50: 4.40E+3nMAssay Description:Inhibitory activity against Candida albicans N-myristoyltransferase (CaNmt)More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2018
Entry Details Article
PubMed