Reaction Details |
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Target | Neuropeptide Y receptor type 2 |
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Ligand | BDBM50346228 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_749573 (CHEMBL1787182) |
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IC50 | >10000±n/a nM |
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Citation | Ando, M; Sato, N; Nagase, T; Nagai, K; Ishikawa, S; Takahashi, H; Ohtake, N; Ito, J; Hirayama, M; Mitobe, Y; Iwaasa, H; Gomori, A; Matsushita, H; Tadano, K; Fujino, N; Tanaka, S; Ohe, T; Ishihara, A; Kanatani, A; Fukami, T Discovery of pyridone-containing imidazolines as potent and selective inhibitors of neuropeptide Y Y5 receptor. Bioorg Med Chem17:6106-22 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Neuropeptide Y receptor type 2 |
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Name: | Neuropeptide Y receptor type 2 |
Synonyms: | NPY-Y2 | NPY-Y2 receptor | NPY2-R | NPY2R | NPY2R_HUMAN | Neuropeptide Y receptor type 2 | Y2 receptor | neuropeptide Y receptor Y2 |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 42734.65 |
Organism: | Homo sapiens (Human) |
Description: | NPY-Y2 NPY2R HUMAN::P49146 |
Residue: | 381 |
Sequence: | MGPIGAEADENQTVEEMKVEQYGPQTTPRGELVPDPEPELIDSTKLIEVQVVLILAYCSI
ILLGVIGNSLVIHVVIKFKSMRTVTNFFIANLAVADLLVNTLCLPFTLTYTLMGEWKMGP
VLCHLVPYAQGLAVQVSTITLTVIALDRHRCIVYHLESKISKRISFLIIGLAWGISALLA
SPLAIFREYSLIEIIPDFEIVACTEKWPGEEKSIYGTVYSLSSLLILYVLPLGIISFSYT
RIWSKLKNHVSPGAANDHYHQRRQKTTKMLVCVVVVFAVSWLPLHAFQLAVDIDSQVLDL
KEYKLIFTVFHIIAMCSTFANPLLYGWMNSNYRKAFLSAFRCEQRLDAIHSEVSVTFKAK
KNLEVRKNSGPNDSFTEATNV
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BDBM50346228 |
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n/a |
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Name | BDBM50346228 |
Synonyms: | 1-(Difluoromethyl)-5-[(4S,5S)-4-(4-fluorophenyl)-4-(6-fluoropyridin-3-yl)-5-methyl-4,5-dihydro-1H-imidazol-2-yl]pyridin-2(1H)-one | CHEMBL1784130 |
Type | Small organic molecule |
Emp. Form. | C21H16F4N4O |
Mol. Mass. | 416.3716 |
SMILES | C[C@@H]1NC(=N[C@@]1(c1ccc(F)cc1)c1ccc(F)nc1)c1ccc(=O)n(c1)C(F)F |r,c:3| |
Structure |
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