Ki Summary

Reaction Details

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Target

Neuropeptide Y receptor type 2

Ligand

BDBM50197022

Substrate/Competitor

n/a

Meas. Tech.

ChEMBL_453177 (CHEMBL902327)

6±n/a nM

Citation

DeCarr, LB; Buckholz, TM; Coish, PD; Fathi, Z; Fisk, SE; Mays, MR; O'Connor, SJ; Lumb, KJ Identification of selective neuropeptide Y2 peptide agonists. Bioorg Med Chem Lett17:538-41 (2007) [PubMed] Article

More Info.:

Get all data from this article, Assay Method

Neuropeptide Y receptor type 2

Name:

Neuropeptide Y receptor type 2

Synonyms:

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

BDBM50197022

n/a

Name

BDBM50197022

Synonyms:

(2S)-2-[(2S)-2-[(2S,3R)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(4-amino-3-methylphenyl)formamido]-5-carbamimidamidopentanamido]-3-(1H-imidazol-5-yl)propanamido]-3-(4-hydroxyphenyl)propanamido]-4-methylpentanamido]-3-carbamoylpropanamido]-4-methylpentanamido]-3-methylbutanamido]-3-hydroxybutanamido]-5-carbamimidamidopentanamido]-N-[(1S)-4-carbamimidamido-1-{[(1S)-1-carbamoyl-2-(4-hydroxyphenyl)ethyl]carbamoyl}butyl]pentanediamide | CHEMBL266814

Type

Small organic molecule

Emp. Form.

C80H123N27O18

Mol. Mass.

1751.0027

SMILES

CC(C)C[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](CCCN=C(N)N)NC(=O)c1ccc(N)c(C)c1)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |wU:75.77,76.80,4.4,93.95,20.28,60.62,113.115,wD:68.70,8.17,30.39,82.84,52.54,102.104,(11.41,4.2,;11.41,2.66,;12.75,1.89,;10.08,1.89,;10.08,.35,;8.74,-.4,;7.4,.36,;7.4,1.9,;6.08,-.41,;6.08,-1.95,;7.4,-2.72,;8.74,-1.95,;10.08,-2.72,;10.08,-4.26,;11.39,-5.02,;8.74,-5.03,;7.4,-4.26,;4.74,.36,;3.41,-.42,;3.41,-1.96,;2.09,.35,;2.09,1.89,;3.41,2.66,;4.82,2.03,;5.86,3.18,;5.09,4.51,;3.58,4.19,;.75,-.41,;-.59,.36,;-.59,1.9,;-1.92,-.41,;-1.92,-1.95,;-.59,-2.72,;-.59,-4.26,;.75,-5.03,;.75,-6.57,;-.6,-7.34,;2.07,-7.34,;-3.25,.35,;-4.58,-.43,;-4.57,-1.97,;-5.91,.33,;-5.91,1.87,;-7.24,2.64,;-8.58,1.87,;-9.91,2.64,;-8.57,.32,;-9.9,-.45,;-7.24,-.44,;11.41,-.42,;11.41,-1.96,;12.74,.36,;14.07,-.41,;14.07,-1.95,;15.4,-2.72,;16.72,-1.94,;15.4,-4.26,;15.4,.36,;15.4,1.9,;16.73,-.41,;18.07,.36,;18.07,1.9,;19.4,2.67,;19.4,4.21,;20.74,1.9,;19.4,-.41,;19.4,-1.95,;20.73,.36,;22.06,-.41,;22.06,-1.95,;23.39,-2.72,;20.73,-2.72,;23.39,.36,;23.39,1.9,;24.73,-.41,;26.06,.36,;26.06,1.9,;24.73,2.67,;27.39,2.68,;27.39,-.41,;27.39,-1.95,;28.72,.37,;30.05,-.41,;30.05,-1.95,;31.38,-2.72,;31.38,-4.26,;32.72,-5.02,;32.72,-6.56,;31.38,-7.32,;34.05,-7.32,;31.38,.36,;31.38,1.9,;32.72,-.4,;34.06,.36,;34.06,1.9,;35.38,2.67,;35.38,4.21,;34.05,4.99,;36.72,4.98,;35.38,-.41,;35.38,-1.95,;36.72,.37,;38.05,-.41,;38.05,-1.95,;39.38,-2.72,;39.38,-4.26,;40.71,-5.02,;40.71,-6.56,;39.38,-7.32,;42.05,-7.32,;39.38,.36,;39.38,1.9,;40.71,-.4,;42.05,.36,;42.05,1.9,;43.38,2.67,;44.71,1.9,;46.05,2.67,;46.05,4.21,;47.38,4.98,;44.71,4.98,;43.38,4.21,;43.38,-.41,;44.71,.36,;43.38,-1.95,)|

Structure