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SB-204070

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
SB-204070
Identifiers
  • (1-butyl-4-piperidinyl)methyl-8-amino-7-chloro-1,4-benzodioxane-5-carboxylate
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC19H27ClN2O4
Molar mass382.89 g·mol−1
3D model (JSmol)
  • Nc1c2OCCOc2c(cc1Cl)C(=O)OCC3CCN(CCCC)CC3
  • InChI=1S/C19H27ClN2O4/c1-2-3-6-22-7-4-13(5-8-22)12-26-19(23)14-11-15(20)16(21)18-17(14)24-9-10-25-18/h11,13H,2-10,12,21H2,1H3
  • Key:AOOSJYIINXVNHV-UHFFFAOYSA-N

SB-204070 is a drug which acts as a potent and selective5-HT4serotoninreceptorantagonist (or weakpartial agonist), and is used for research into the function of this receptor subtype.[1][2][3][4][5]

References

[edit]
  1. ^Mialet J, Berque-Bestel I, Sicsic S, Langlois M, Fischmeister R, Lezoualc'h F (October 2000)."Pharmacological characterization of the human 5-HT(4(d)) receptor splice variant stably expressed in Chinese hamster ovary cells".British Journal of Pharmacology.131 (4):827–35.doi:10.1038/sj.bjp.0703641.PMC 1572397.PMID 11030734.
  2. ^Pindon A, van Hecke G, van Gompel P, Lesage AS, Leysen JE, Jurzak M (January 2002). "Differences in signal transduction of two 5-HT4 receptor splice variants: compound specificity and dual coupling with Galphas- and Galphai/o-proteins".Molecular Pharmacology.61 (1):85–96.doi:10.1124/mol.61.1.85.PMID 11752209.S2CID 85908752.
  3. ^Takahashi H, Takada Y, Urano T, Takada A (2002). "5-HT4 receptors in the hippocampus modulate rat locomotor activity".Hippocampus.12 (3):304–10.doi:10.1002/hipo.10012.PMID 12099482.S2CID 19746691.
  4. ^Sakurai-Yamashita Y, Yamashita K, Niwa M, Taniyama K (May 2003). "Involvement of 5-hydroxytryptamine4 receptor in the exacerbation of neuronal loss by psychological stress in the hippocampus of SHRSP with a transient ischemia".Brain Research.973 (1):92–8.doi:10.1016/S0006-8993(03)02559-9.PMID 12729957.S2CID 22136959.
  5. ^Smith AJ, Chappell AE, Buret AG, Barrett KE, Dong H (December 2006)."5-Hydroxytryptamine contributes significantly to a reflex pathway by which the duodenal mucosa protects itself from gastric acid injury".FASEB Journal.20 (14):2486–95.doi:10.1096/fj.06-6391com.PMID 17142798.S2CID 27119792.
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
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