Reaction Details |
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Target | Fatty-acid amide hydrolase 1 |
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Ligand | BDBM50128572 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_762794 (CHEMBL1816096) |
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IC50 | >30000±n/a nM |
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Citation | Otrubova, K; Ezzili, C; Boger, DL The discovery and development of inhibitors of fatty acid amide hydrolase (FAAH). Bioorg Med Chem Lett21:4674-85 (2011) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Fatty-acid amide hydrolase 1 |
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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
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BDBM50128572 |
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n/a |
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Name | BDBM50128572 |
Synonyms: | 1-Naphthalenol, methylcarbamate | 1-Naphthalenyl methylcarbamate | 1-Naphthyl N-methylcarbamate | CHEMBL46917 | Carbaril | Carbaryl | N-Methyl-1-naphthyl carbamate | N-Methyl-alpha-naphthylurethan | Sevin | alpha-Naphthyl N-methylcarbamate | cid_6129 | naphthalen-1-yl methylcarbamate |
Type | Small organic molecule |
Emp. Form. | C12H11NO2 |
Mol. Mass. | 201.2212 |
SMILES | CNC(=O)Oc1cccc2ccccc12 |
Structure |
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