Reaction Details |
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Target | Neuropeptide Y receptor type 1 |
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Ligand | BDBM50500159 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1543512 (CHEMBL3750359) |
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Ki | 3.1±n/a nM |
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Citation | Keller, M; Weiss, S; Hutzler, C; Kuhn, KK; Mollereau, C; Dukorn, S; Schindler, L; Bernhardt, G; König, B; Buschauer, A N(?)-Carbamoylation of the Argininamide Moiety: An Avenue to Insurmountable NPY Y1 Receptor Antagonists and a Radiolabeled Selective High-Affinity Molecular Tool ([(3)H]UR-MK299) with Extended Residence Time. J Med Chem58:8834-49 (2015) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Neuropeptide Y receptor type 1 |
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Name: | Neuropeptide Y receptor type 1 |
Synonyms: | NPY-Y1 | NPY1-R | NPY1R | NPY1R_HUMAN | NPYR | NPYY1 | neuropeptide Y receptor Y1 |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 44399.07 |
Organism: | Homo sapiens (Human) |
Description: | NPY-Y1 NPY1R HUMAN::P25929 |
Residue: | 384 |
Sequence: | MNSTLFSQVENHSVHSNFSEKNAQLLAFENDDCHLPLAMIFTLALAYGAVIILGVSGNLA
LIIIILKQKEMRNVTNILIVNLSFSDLLVAIMCLPFTFVYTLMDHWVFGEAMCKLNPFVQ
CVSITVSIFSLVLIAVERHQLIINPRGWRPNNRHAYVGIAVIWVLAVASSLPFLIYQVMT
DEPFQNVTLDAYKDKYVCFDQFPSDSHRLSYTTLLLVLQYFGPLCFIFICYFKIYIRLKR
RNNMMDKMRDNKYRSSETKRINIMLLSIVVAFAVCWLPLTIFNTVFDWNHQIIATCNHNL
LFLLCHLTAMISTCVNPIFYGFLNKNFQRDLQFFFNFCDFRSRDDDYETIAMSTMHTDVS
KTSLKQASPVAFKKINNNDDNEKI
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BDBM50500159 |
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n/a |
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Name | BDBM50500159 |
Synonyms: | CHEMBL3746893 |
Type | Small organic molecule |
Emp. Form. | C39H39F3N12O6 |
Mol. Mass. | 828.799 |
SMILES | OC(=O)C(F)(F)F.N\C(NCCC[C@@H](NC(=O)C(c1ccccc1)c1ccccc1)C(=O)NCc1ccc(O)cc1)=N\C(=O)NCc1cn(nn1)-c1cccc(c1)N=[N+]=[N-] |r| |
Structure |
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