Reaction Details |
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Target | Neuropeptide Y receptor type 1 |
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Ligand | BDBM50060722 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_143827 (CHEMBL748712) |
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Ki | 26±n/a nM |
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Citation | Hipskind, PA; Lobb, KL; Nixon, JA; Britton, TC; Bruns, RF; Catlow, J; Dieckman-McGinty, DK; Gackenheimer, SL; Gitter, BD; Iyengar, S; Schober, DA; Simmons, RM; Swanson, S; Zarrinmayeh, H; Zimmerman, DM; Gehlert, DR Potent and selective 1,2,3-trisubstituted indole NPY Y-1 antagonists. J Med Chem40:3712-4 (1997) [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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BDBM50060722 |
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n/a |
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Name | BDBM50060722 |
Synonyms: | 2-[1,4']Bipiperidinyl-1'-yl-1-[2-(4-chloro-phenoxymethyl)-1-methyl-1H-indol-3-yl]-ethanone | CHEMBL124343 |
Type | Small organic molecule |
Emp. Form. | C28H34ClN3O2 |
Mol. Mass. | 480.041 |
SMILES | Cn1c(COc2ccc(Cl)cc2)c(C(=O)CN2CCC(CC2)N2CCCCC2)c2ccccc12 |
Structure |
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