TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Concordia University Wisconsin
Curated by ChEMBL
Concordia University Wisconsin
Curated by ChEMBL
Affinity DataIC50: 1.03E+4nMAssay Description:Inhibition of recombinant human FAAH using N-arachidonyl-7-amino-4-methylcoumarin as substrate preincubated for 20 mins followed by substrate additio...More data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Concordia University Wisconsin
Curated by ChEMBL
Concordia University Wisconsin
Curated by ChEMBL
Affinity DataIC50: 1.08E+4nMAssay Description:Inhibition of recombinant human FAAH using N-arachidonyl-7-amino-4-methylcoumarin as substrate preincubated for 20 mins followed by substrate additio...More data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Concordia University Wisconsin
Curated by ChEMBL
Concordia University Wisconsin
Curated by ChEMBL
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of recombinant human FAAH using N-arachidonyl-7-amino-4-methylcoumarin as substrate preincubated for 20 mins followed by substrate additio...More data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Concordia University Wisconsin
Curated by ChEMBL
Concordia University Wisconsin
Curated by ChEMBL
Affinity DataIC50: 1.37E+4nMAssay Description:Inhibition of recombinant human FAAH using N-arachidonyl-7-amino-4-methylcoumarin as substrate preincubated for 20 mins followed by substrate additio...More data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Concordia University Wisconsin
Curated by ChEMBL
Concordia University Wisconsin
Curated by ChEMBL
Affinity DataIC50: 1.67E+4nMAssay Description:Inhibition of recombinant human FAAH using N-arachidonyl-7-amino-4-methylcoumarin as substrate preincubated for 20 mins followed by substrate additio...More data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Concordia University Wisconsin
Curated by ChEMBL
Concordia University Wisconsin
Curated by ChEMBL
Affinity DataIC50: 4.18E+4nMAssay Description:Inhibition of recombinant human FAAH using N-arachidonyl-7-amino-4-methylcoumarin as substrate preincubated for 20 mins followed by substrate additio...More data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Concordia University Wisconsin
Curated by ChEMBL
Concordia University Wisconsin
Curated by ChEMBL
Affinity DataIC50: 5.00E+5nMAssay Description:Inhibition of recombinant human FAAH using N-arachidonyl-7-amino-4-methylcoumarin as substrate preincubated for 20 mins followed by substrate additio...More data for this Ligand-Target Pair