BDBM50157120 (9Z)-1-(5-pyridin-2-yl-1,3,4-oxadiazol-2-yl)octadec-9-en-1-one::(Z)-1-(5-(pyridin-2-yl)-1,3,4-oxadiazol-2-yl)octadec-9-en-1-one::(Z)-1-(5-Pyridin-2-yl-[1,3,4]oxadiazol-2-yl)-octadec-9-en-1-one::1-(5-(pyridin-2-yl)-1,3,4-oxadiazol-2-yl)octadec-9-en-1-one::1-(5-Pyridin-2-yl-[1,3,4]oxadiazol-2-yl)-octadec-9-en-1-one::CHEMBL178563
SMILES: CCCCCCCC\C=C/CCCCCCCC(=O)c1nnc(o1)-c1ccccn1
InChI Key: InChIKey=SUSLQAWJWPTQHX-KTKRTIGZSA-N
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Fatty-acid amide hydrolase 1 (aa 30-579) (Rattus norvegicus (rat)) | BDBM50157120 ((9Z)-1-(5-pyridin-2-yl-1,3,4-oxadiazol-2-yl)octade...) | PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid PDB UniChem Patents Similars | Article PubMed | 3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute Curated by ChEMBL | Assay Description Binding affinity against purified rat Fatty-acid amide hydrolase (FAAH) expressed in Escherichia coli | Bioorg Med Chem Lett 15: 103-6 (2004) Article DOI: 10.1016/j.bmcl.2004.10.025 BindingDB Entry DOI: 10.7270/Q2MC8ZGW | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Anandamide amidohydrolase (Mus musculus (mouse)) | BDBM50157120 ((9Z)-1-(5-pyridin-2-yl-1,3,4-oxadiazol-2-yl)octade...) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid PDB UniChem Patents Similars | PDB Article PubMed | 3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute Curated by ChEMBL | Assay Description Inhibitor affinity of the compound towards enzymes of class serine hydrolase was determined using biotin or fluorescent as radioligand (FP-biotin or ... | Bioorg Med Chem Lett 15: 1423-8 (2005) Article DOI: 10.1016/j.bmcl.2004.12.085 BindingDB Entry DOI: 10.7270/Q2PK0FNK | |||||||||||
More data for this Ligand-Target Pair | 3D Structure (crystal) | ||||||||||||
Fatty-acid amide hydrolase 1 (aa 30-579) (Rattus norvegicus (rat)) | BDBM50157120 ((9Z)-1-(5-pyridin-2-yl-1,3,4-oxadiazol-2-yl)octade...) | PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid PDB UniChem Patents Similars | Article PubMed | 3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Institute for Chemical Biology Curated by ChEMBL | Assay Description Inhibition of rat FAAH expressed in Escherichia coli | J Med Chem 51: 4392-403 (2008) Article DOI: 10.1021/jm800136b BindingDB Entry DOI: 10.7270/Q26D5TW3 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Fatty-acid amide hydrolase 1 (aa 30-579) (Rattus norvegicus (rat)) | BDBM50157120 ((9Z)-1-(5-pyridin-2-yl-1,3,4-oxadiazol-2-yl)octade...) | PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid PDB UniChem Patents Similars | Article PubMed | 3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL | Assay Description Inhibition of rat FAAH | Bioorg Med Chem 16: 1562-95 (2008) Article DOI: 10.1016/j.bmc.2007.11.015 BindingDB Entry DOI: 10.7270/Q21J9BNH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Acyl-CoA: cholesterol acyltransferase (ACAT) (Homo sapiens (Human)) | BDBM50157120 ((9Z)-1-(5-pyridin-2-yl-1,3,4-oxadiazol-2-yl)octade...) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet | CHEMBL PC cid PC sid PDB UniChem Patents Similars | Article PubMed | n/a | n/a | 2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute Curated by ChEMBL | Assay Description Inhibitory concentration of triacylgylcerol hydrolase using FP-Rh radioligand | Bioorg Med Chem Lett 15: 1423-8 (2005) Article DOI: 10.1016/j.bmcl.2004.12.085 BindingDB Entry DOI: 10.7270/Q2PK0FNK | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Fatty-acid amide hydrolase 1 (Homo sapiens (Human)) | BDBM50157120 ((9Z)-1-(5-pyridin-2-yl-1,3,4-oxadiazol-2-yl)octade...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid PDB UniChem Patents Similars | PDB Article PubMed | n/a | n/a | 4 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute Curated by ChEMBL | Assay Description Inhibitory concentration of fatty acid amide hydrolase using FP-Rh radioligand | Bioorg Med Chem Lett 15: 1423-8 (2005) Article DOI: 10.1016/j.bmcl.2004.12.085 BindingDB Entry DOI: 10.7270/Q2PK0FNK | |||||||||||
More data for this Ligand-Target Pair | 3D Structure (crystal) |