BDBM50439659 CHEMBL2419824::US9353075, 1

SMILES CCCCCOC(=O)N[C@@H]1[C@H](C)OC1=O

InChI Key InChIKey=HZDBYMSLJOAPIN-JGVFFNPUSA-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 = 50439659   

TargetN-acylethanolamine-hydrolyzing acid amidase(Rattus norvegicus (Rat))
University Of California

US Patent
LigandPNGBDBM50439659(CHEMBL2419824 | US9353075, 1)
Affinity DataIC50:  670nMpH: 7.4Assay Description:Lysosomal NAAA protein preparation were obtained by homogenizing male Sprague-Dawley rat lungs (Charles River) in 20 mM Tris-HCl buffer pH 7.4 contai...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetN-acylethanolamine-hydrolyzing acid amidase(Rattus norvegicus (Rat))
University Of California

US Patent
LigandPNGBDBM50439659(CHEMBL2419824 | US9353075, 1)
Affinity DataIC50:  760nMAssay Description:Inhibition of Sprague Dawley rat lung native NAAA enzyme using heptadecenoylethanolamide as substrate preincubated for 30 mins followed by substrate ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-acylethanolamine-hydrolyzing acid amidase(Rattus norvegicus (Rat))
University Of California

US Patent
LigandPNGBDBM50439659(CHEMBL2419824 | US9353075, 1)
Affinity DataIC50:  460nMAssay Description:Inhibition of NAAA in Sprague-Dawley rat lung assessed as inhibition of hydrolysis of 10-cis-heptadecenoylethanolamide by UPLC/MS methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-acylethanolamine-hydrolyzing acid amidase(Rattus norvegicus (Rat))
University Of California

US Patent
LigandPNGBDBM50439659(CHEMBL2419824 | US9353075, 1)
Affinity DataIC50:  460nMAssay Description:Inhibition of NAAA in Sprague-Dawley rat lung assessed as inhibition of hydrolysis of 10-cis-heptadecenoylethanolamide by UPLC/MS methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed