Reaction Details |
| Report a problem with these data |
Target | Fatty-acid amide hydrolase 1 |
---|
Ligand | BDBM26144 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_68777 (CHEMBL686015) |
---|
Ki | 5000±n/a nM |
---|
Citation | van der Stelt, M; van Kuik, JA; Bari, M; van Zadelhoff, G; Leeflang, BR; Veldink, GA; Finazzi-Agrò, A; Vliegenthart, JF; Maccarrone, M Oxygenated metabolites of anandamide and 2-arachidonoylglycerol: conformational analysis and interaction with cannabinoid receptors, membrane transporter, and fatty acid amide hydrolase. J Med Chem45:3709-20 (2002) [PubMed] |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Fatty-acid amide hydrolase 1 |
---|
Name: | Fatty-acid amide hydrolase 1 |
Synonyms: | Anandamide amidohydrolase | Anandamide amidohydrolase 1 | FAAH | FAAH1 | FAAH1_HUMAN | Fatty Acid Amide Hydrolase (FAAH) | Fatty-acid amide hydrolase (FAAH) | Fatty-acid amide hydrolase 1 | Oleamide hydrolase 1 |
Type: | Protein |
Mol. Mass.: | 63071.19 |
Organism: | Homo sapiens (Human) |
Description: | O00519 |
Residue: | 579 |
Sequence: | MVQYELWAALPGASGVALACCFVAAAVALRWSGRRTARGAVVRARQRQRAGLENMDRAAQ
RFRLQNPDLDSEALLALPLPQLVQKLHSRELAPEAVLFTYVGKAWEVNKGTNCVTSYLAD
CETQLSQAPRQGLLYGVPVSLKECFTYKGQDSTLGLSLNEGVPAECDSVVVHVLKLQGAV
PFVHTNVPQSMFSYDCSNPLFGQTVNPWKSSKSPGGSSGGEGALIGSGGSPLGLGTDIGG
SIRFPSSFCGICGLKPTGNRLSKSGLKGCVYGQEAVRLSVGPMARDVESLALCLRALLCE
DMFRLDPTVPPLPFREEVYTSSQPLRVGYYETDNYTMPSPAMRRAVLETKQSLEAAGHTL
VPFLPSNIPHALETLSTGGLFSDGGHTFLQNFKGDFVDPCLGDLVSILKLPQWLKGLLAF
LVKPLLPRLSAFLSNMKSRSAGKLWELQHEIEVYRKTVIAQWRALDLDVVLTPMLAPALD
LNAPGRATGAVSYTMLYNCLDFPAGVVPVTTVTAEDEAQMEHYRGYFGDIWDKMLQKGMK
KSVGLPVAVQCVALPWQEELCLRFMREVERLMTPEKQSS
|
|
|
BDBM26144 |
---|
n/a |
---|
Name | BDBM26144 |
Synonyms: | 1,3-dihydroxypropan-2-yl (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoate | 2-Arachidonoylmonoglycerol (2-AG) | 2-arachidonoylglycerol (2-AG) | 2-arachidonyl-glycerol | CHEMBL122972 |
Type | Endocannabinoids |
Emp. Form. | C23H38O4 |
Mol. Mass. | 378.5454 |
SMILES | CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)OC(CO)CO |
Structure |
|