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TargetNeuropeptide Y receptor type 1
LigandBDBM50273943
Substrate/Competitorn/a
Meas. Tech.ChEMBL_537978 (CHEMBL1032434)
Ki>50000±n/a nM
Citation Weiss, SKeller, MBernhardt, GBuschauer, AKönig, B Modular synthesis of non-peptidic bivalent NPY Y1 receptor antagonists. Bioorg Med Chem16:9858-66 (2008) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Neuropeptide Y receptor type 1
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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BDBM50273943
n/a
NameBDBM50273943
Synonyms:(Ammoniotris{methylene-1H-1,2,3-triazole-4,1-diylmethylene-4,1-phenylenecarbonylimino[({4-[(diphenylacetyl)amino]-5-[(4-hydroxybenzyl)amino]-5-oxopentyl}amino)methylylidene]})triammonium tetrakis(trifluoroacetate) | CHEMBL526676
TypeSmall organic molecule
Emp. Form.C114H121N25O12
Mol. Mass.2033.3386
SMILES[NH3+]C(NC(=O)c1ccc(Cn2cc(C[NH+](Cc3cn(Cc4ccc(cc4)C(=O)NC([NH3+])=NCCC[C@@H](NC(=O)C(c4ccccc4)c4ccccc4)C(=O)NCc4ccc(O)cc4)nn3)Cc3cn(Cc4ccc(cc4)C(=O)NC([NH3+])=NCCC[C@@H](NC(=O)C(c4ccccc4)c4ccccc4)C(=O)NCc4ccc(O)cc4)nn3)nn2)cc1)=NCCC[C@@H](NC(=O)C(c1ccccc1)c1ccccc1)C(=O)NCc1ccc(O)cc1 |r,w:31.32,119.131,81.87|
Structure
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