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TargetNeuropeptide Y receptor type 5
LigandBDBM50304312
Substrate/Competitorn/a
Meas. Tech.ChEMBL_606453 (CHEMBL1074018)
IC50 2.1±n/a nM
Citation Haga, YSakamoto, TShibata, TNonoshita, KIshikawa, MSuga, TTakahashi, HTakahashi, TTakahashi, HAndo, MMurai, TGomori, AOda, ZKitazawa, HMitobe, YKanesaka, MOhe, TIwaasa, HIshii, YIshihara, AKanatani, AFukami, T Discovery of trans-N-[1-(2-fluorophenyl)-3-pyrazolyl]-3-oxospiro[6-azaisobenzofuran-1(3H),1'-cyclohexane]-4'-carboxamide, a potent and orally active neuropeptide Y Y5 receptor antagonist. Bioorg Med Chem17:6971-82 (2009) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Neuropeptide Y receptor type 5
Name:Neuropeptide Y receptor type 5
Synonyms:NPY-Y5 | NPY-Y5 receptor | NPY5-R | NPY5R | NPY5R_HUMAN | NPYR5 | NPYY5 | Neuropeptide Y receptor type 5 | Neuropeptide Y receptor type 5 ( NPY Y5) | Y5 receptor
Type:Enzyme
Mol. Mass.:50746.64
Organism:Homo sapiens (Human)
Description:Q15761
Residue:445
Sequence:
MDLELDEYYNKTLATENNTAATRNSDFPVWDDYKSSVDDLQYFLIGLYTFVSLLGFMGNL
LILMALMKKRNQKTTVNFLIGNLAFSDILVVLFCSPFTLTSVLLDQWMFGKVMCHIMPFL
QCVSVLVSTLILISIAIVRYHMIKHPISNNLTANHGYFLIATVWTLGFAICSPLPVFHSL
VELQETFGSALLSSRYLCVESWPSDSYRIAFTISLLLVQYILPLVCLTVSHTSVCRSISC
GLSNKENRLEENEMINLTLHPSKKSGPQVKLSGSHKWSYSFIKKHRRRYSKKTACVLPAP
ERPSQENHSRILPENFGSVRSQLSSSSKFIPGVPTCFEIKPEENSDVHELRVKRSVTRIK
KRSRSVFYRLTILILVFAVSWMPLHLFHVVTDFNDNLISNRHFKLVYCICHLLGMMSCCL
NPILYGFLNNGIKADLVSLIHCLHM
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  Blast E-value cutoff:
BDBM50304312
n/a
NameBDBM50304312
Synonyms:CHEMBL604480 | trans-3-Oxo-N-(5-phenylpyridin-2-yl)-3H-spiro[6-aza-2-benzofuran-1,1'-cyclohexane]-4'-carboxamide
TypeSmall organic molecule
Emp. Form.C24H21N3O3
Mol. Mass.399.4418
SMILESO=C(Nc1ccc(cn1)-c1ccccc1)[C@H]1CC[C@@]2(CC1)OC(=O)c1ccncc21 |r,wU:18.23,wD:15.16,(24.78,5.17,;25.55,3.84,;27.09,3.84,;27.93,2.54,;27.22,1.18,;28.05,-.12,;29.59,-.04,;30.29,1.34,;29.45,2.63,;30.43,-1.33,;29.72,-2.7,;30.56,-3.99,;32.1,-3.92,;32.8,-2.53,;31.96,-1.25,;24.78,2.51,;23.24,2.51,;22.47,1.17,;23.24,-.16,;24.78,-.16,;25.55,1.17,;24.16,-1.41,;23.25,-2.67,;23.72,-4.13,;21.77,-2.19,;20.44,-2.96,;19.11,-2.19,;19.11,-.65,;20.44,.13,;21.77,-.64,)|
Structure
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