5-HT4受體

5-HT4受體
标识符
代号HTR4
扩展标识OMIM602164MGI109246;HomoloGene:20243GeneCardsHTR4;OMA:HTR4 - orthologs
直系同源
物種人類小鼠
Entrez
3360
15562
Ensembl
ENSG00000164270
ENSMUSG00000026322
UniProt
Q13639
P97288
mRNA序列
NM_008313
​NM_001364956
​NM_001364957
​NM_001364958
​NM_001364959
蛋白序列
NP_032339
​NP_001351885
​NP_001351886
​NP_001351887
​NP_001351888
基因位置Chr 5:148.45 – 148.68 MbChr 18:62.46 – 62.63 Mb
PubMed查询[3][4]
维基数据
檢視/編輯人類檢視/編輯小鼠

5-HT4受體5-羥色胺受體4(英語:5-Hydroxytryptamine receptor 4)是在人類上由HTR4基因編碼的蛋白質[5][6]

配體

激動劑

拮抗劑

  • Piboserod
  • GR-113,808 (1-methyl-1H-indole-3-carboxylic acid, [1-[2-[(methylsulfonyl)amino]ethyl]-4-piperidinyl]methyl ester)[8]
  • GR-125,487
  • RS-39604 (1-[4-Amino-5-chloro-2-(3,5-dimethoxyphenyl)methyloxy]-3-[1-[2-methylsulphonylamino]piperidin-4-yl]propan-1-one)
  • SB-203,186
  • SB-204,070
  • ([Methoxy-11C]1-butylpiperidin-4-yl)methyl 4-amino-3-methoxybenzoate[9]
  • 洋甘菊(酒精萃取)[10]

參見

參考資料

  1. ^ 1.0 1.1 1.2 GRCh38: Ensembl release 89: ENSG00000164270 – Ensembl, May 2017
  2. ^ 2.0 2.1 2.2 GRCm38: Ensembl release 89: ENSMUSG00000026322Ensembl, 2017年5月
  3. ^ Human PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine. 
  4. ^ Mouse PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine. 
  5. ^ Claeysen S, Faye P, Sebben M, Lemaire S, Bockaert J, Dumuis A, Taviaux S. Assignment of 5-hydroxytryptamine receptor (HTR4) to human chromosome 5 bands q31-->q33 by in situ hybridization. Cytogenetics and Cell Genetics. December 1997, 78 (2): 133–4. PMID 9371406. doi:10.1159/000134646. 
  6. ^ Blondel O, Vandecasteele G, Gastineau M, Leclerc S, Dahmoune Y, Langlois M, Fischmeister R. Molecular and functional characterization of a 5-HT4 receptor cloned from human atrium. FEBS Letters. August 1997, 412 (3): 465–74. PMID 9276448. doi:10.1016/S0014-5793(97)00820-X. 
  7. ^ Godínez-Chaparro B, Barragán-Iglesias P, Castañeda-Corral G, Rocha-González HI, Granados-Soto V. Role of peripheral 5-HT(4), 5-HT(6), and 5-HT(7) receptors in development and maintenance of secondary mechanical allodynia and hyperalgesia. Pain. March 2011, 152 (3): 687–97. PMID 21239110. doi:10.1016/j.pain.2010.12.020. 
  8. ^ Gale JD, Grossman CJ, Whitehead JW, Oxford AW, Bunce KT, Humphrey PP. GR113808: a novel, selective antagonist with high affinity at the 5-HT4 receptor. British Journal of Pharmacology. January 1994, 111 (1): 332–8. PMC 1910004可免费查阅. PMID 8012715. doi:10.1111/j.1476-5381.1994.tb14064.x. 
  9. ^ Xu R, Hong J, Morse CL, Pike VW. Synthesis, structure-affinity relationships, and radiolabeling of selective high-affinity 5-HT4 receptor ligands as prospective imaging probes for positron emission tomography. Journal of Medicinal Chemistry. October 2010, 53 (19): 7035–47. PMC 2951497可免费查阅. PMID 20812727. doi:10.1021/jm100668r. 
  10. ^ Simmen U, Kelber O, Okpanyi SN, Jaeggi R, Bueter B, Weiser D. Binding of STW 5 (Iberogast) and its components to intestinal 5-HT, muscarinic M3, and opioid receptors. Phytomedicine: 51–5. PMID 16973340. doi:10.1016/j.phymed.2006.03.012. 

深入閱讀

外部連結

  • 5-HT4. IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology. (原始内容存档于2016-06-05). 


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