BDBM319789 US10174015, Compound 2

SMILES O=C(CCCCCc1ccccc1)N1CCOC1=O

InChI Key InChIKey=OXZXDYAGMMUIBN-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 319789   

TargetN-acylethanolamine-hydrolyzing acid amidase(Homo sapiens (Human))
Xiamen University

US Patent
LigandPNGBDBM319789(US10174015, Compound 2)
Affinity DataIC50:  210nMAssay Description:In the Experimental example, endocannabinoid hydrolases used were Fatty Acid Amide Hydrolase (FAAH) and N-acylethanolamide hydrolyzing acid amidase (...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetAcid ceramidase(Rattus norvegicus (Rat))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM319789(US10174015, Compound 2)
Affinity DataIC50:  270nMAssay Description:Inhibition of rat acid ceramidase expressed in HEK293 cells using N-lauroylceramide as substrate after 30 mins by LC-MS analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Xiamen University

US Patent
LigandPNGBDBM319789(US10174015, Compound 2)
Affinity DataIC50: >1.00E+5nMAssay Description:In the Experimental example, endocannabinoid hydrolases used were Fatty Acid Amide Hydrolase (FAAH) and N-acylethanolamide hydrolyzing acid amidase (...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent