BDBM50336283 3-[3'-(4-cyclopent-2'''-en-1'''-ylphenoxy)-2'-hydroxypropyl]-5,5-dimethylimidazolidine-2,4-dione::CHEMBL1669811

SMILES CC1(C)NC(=O)N(CC(O)COc2ccc(cc2)C2CCCC2)C1=O

InChI Key InChIKey=WULAWOWBKGPGCA-UHFFFAOYSA-N

Data  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50336283   

TargetArylamine N-acetyltransferase(Mycobacterium smegmatis)
University Of Oxford

Curated by ChEMBL
LigandPNGBDBM50336283(3-[3'-(4-cyclopent-2'''-en-1'''-ylphenoxy)-2'-hydr...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Mycobacterium smegmatis NAT using isoniazed substrate by acetyl-coA hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetArylamine N-acetyltransferase(Pseudomonas aeruginosa)
University Of Oxford

Curated by ChEMBL
LigandPNGBDBM50336283(3-[3'-(4-cyclopent-2'''-en-1'''-ylphenoxy)-2'-hydr...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Pseudomonas aeruginosa NAT using 5-aminosalicylate substrate by acetyl-coA hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetArylamine N-acetyltransferase(Pseudomonas aeruginosa)
University Of Oxford

Curated by ChEMBL
LigandPNGBDBM50336283(3-[3'-(4-cyclopent-2'''-en-1'''-ylphenoxy)-2'-hydr...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Pseudomonas aeruginosa NAT using isoniazed substrate by acetyl-coA hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetArylamine N-acetyltransferase(Mycobacterium smegmatis)
University Of Oxford

Curated by ChEMBL
LigandPNGBDBM50336283(3-[3'-(4-cyclopent-2'''-en-1'''-ylphenoxy)-2'-hydr...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Mycobacterium smegmatis NAT using 5-aminosalicylate substrate by acetyl-coA hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed