Neuropeptidni Y receptor Y5

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Neuropeptidni Y receptor tip 5 je protein koji je kod ljudi kodiran NPY5R genom.[1][2][3]

Neuropeptidni Y receptor Y5
Identifikatori
SimboliNPY5R; NPYR5
Vanjski IDOMIM602001 MGI108082 HomoloGene21241 IUPHAR: Y5 GeneCards: NPY5R Gene
Pregled RNK izražavanja
podaci
Ortolozi
VrstaČovekMiš
Entrez488918168
EnsemblENSG00000164129ENSMUSG00000044014
UniProtQ15761Q543U8
RefSeq (mRNA)NM_006174NM_016708
RefSeq (protein)NP_006165NP_057917
Lokacija (UCSC)Chr 4:
164.48 - 164.49 Mb
Chr 8:
69.61 - 69.62 Mb
PubMed pretraga[1][2]

Selektivni ligandi uredi

Agonisti uredi

Antagonisti uredi

Vidi još uredi

Reference uredi

  1. Gerald C, Walker MW, Criscione L, Gustafson EL, Batzl-Hartmann C, Smith KE, Vaysse P, Durkin MM, Laz TM, Linemeyer DL, Schaffhauser AO, Whitebread S, Hofbauer KG, Taber RI, Branchek TA, Weinshank RL (Aug 1996). „A receptor subtype involved in neuropeptide-Y-induced food intake”. Nature 382 (6587): 168–71. DOI:10.1038/382168a0. PMID 8700207. 
  2. Lutz CM, Richards JE, Scott KL, Sinha S, Yang-Feng TL, Frankel WN, Thompson DA (Feb 1998). „Neuropeptide Y receptor genes mapped in human and mouse: receptors with high affinity for pancreatic polypeptide are not clustered with receptors specific for neuropeptide Y and peptide YY”. Genomics 46 (2): 287–90. DOI:10.1006/geno.1997.5024. PMID 9417917. 
  3. „Entrez Gene: NPY5R neuropeptide Y receptor Y5”. 
  4. Kakui N, Tanaka J, Tabata Y, Asai K, Masuda N, Miyara T, Nakatani Y, Ohsawa F, Nishikawa N, Sugai M, Suzuki M, Aoki K, Kitaguchi H (May 2006). „Pharmacological characterization and feeding-suppressive property of FMS586 [3-(5,6,7,8-tetrahydro-9-isopropyl-carbazol-3-yl)-1-methyl-1-(2-pyridin-4-yl-ethyl)-urea hydrochloride], a novel, selective, and orally active antagonist for neuropeptide Y Y5 receptor”. The Journal of Pharmacology and Experimental Therapeutics 317 (2): 562–70. DOI:10.1124/jpet.105.099705. PMID 16436501. 
  5. Walker MW, Wolinsky TD, Jubian V, Chandrasena G, Zhong H, Huang X, Miller S, Hegde LG, Marsteller DA, Marzabadi MR, Papp M, Overstreet DH, Gerald CP, Craig DA (March 2009). „The novel neuropeptide Y Y5 receptor antagonist Lu AA33810 (N-([trans-4-[(4,5-dihydro[1benzothiepino[5,4-d]thiazol-2-yl)amino]cyclohexyl]methyl)-methanesulfonamide) exerts anxiolytic- and antidepressant-like effects in rat models of stress sensitivity”]. The Journal of Pharmacology and Experimental Therapeutics 328 (3): 900–11. DOI:10.1124/jpet.108.144634. PMID 19098165. 
  6. MacNeil DJ (2007). „NPY Y1 and Y5 receptor selective antagonists as anti-obesity drugs”. Current Topics in Medicinal Chemistry 7 (17): 1721–33. DOI:10.2174/156802607782341028. PMID 17979781. Arhivirano iz originala na datum 2013-01-12. Pristupljeno 2021-10-05. 
  7. Islam I, Dhanoa D, Finn J, Du P, Walker MW, Salon JA, Zhang J, Gluchowski C (July 2002). „Discovery of potent and selective small molecule NPY Y5 receptor antagonists”. Bioorganic & Medicinal Chemistry Letters 12 (13): 1767–9. DOI:10.1016/S0960-894X(02)00287-1. PMID 12067557. 

Literatura uredi