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SB-236057

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
SB-236057
Clinical data
ATC code
  • none
Identifiers
  • 1'-ethyl-5-[2'-methyl-4'-(5-methyl-1,3,4-oxadiazolyl-2-yl)biphenyl-4-carbonyl]-2,3,6,7-tetrahydrospiro(furo[2,3-f]indole-3,4'-piperidine)
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC33H34N4O3
Molar mass534.660 g·mol−1
3D model (JSmol)
  • n5nc(C)oc5-c(cc2C)ccc2-c6ccc(cc6)C(=O)N(CCc1cc3OC7)c1cc3C7(CC4)CCN4CC
  • InChI=1S/C33H34N4O3/c1-4-36-15-12-33(13-16-36)20-39-30-18-25-11-14-37(29(25)19-28(30)33)32(38)24-7-5-23(6-8-24)27-10-9-26(17-21(27)2)31-35-34-22(3)40-31/h5-10,17-19H,4,11-16,20H2,1-3H3
  • Key:WXAKEEQOWUHGCI-UHFFFAOYSA-N

SB-236057 is a compound which is a potent andselectiveinverse agonist for theserotoninreceptor5-HT1B, acting especially at 5-HT1B autoreceptors on nerve terminals. It produces a rapid increase inserotonin levels in the brain, and was originally researched as a potentialantidepressant.[1][2] However subsequent research found that SB-236,057 also acts as a potentteratogen, producing severe musculoskeletal birth defects when rodents were exposed to it during pregnancy. This has made it of little use for research into its original applications, yet has made it useful for studying embryonic development instead.[3][4]

See also

[edit]

References

[edit]
  1. ^Middlemiss DN, Göthert M, Schlicker E, Scott CM, Selkirk JV, Watson J, et al. (June 1999). "SB-236057, a selective 5-HT1B receptor inverse agonist, blocks the 5-HT human terminal autoreceptor".European Journal of Pharmacology.375 (1–3):359–65.doi:10.1016/s0014-2999(99)00262-9.PMID 10443589.
  2. ^Roberts C, Watson J, Price GW, Middlemiss DN (2006)."SB-236057-A: a selective 5-HT1B receptor inverse agonist".CNS Drug Reviews.7 (4):433–44.doi:10.1111/j.1527-3458.2001.tb00209.x.PMC 6741665.PMID 11830759.
  3. ^Augustine-Rauch KA, Zhang QJ, Posobiec L, Mirabile R, DeBoer LS, Solomon HM, Wier PJ (October 2004). "SB-236057: Critical window of sensitivity study and embryopathy of a potent musculoskeletal teratogen".Birth Defects Research. Part A, Clinical and Molecular Teratology.70 (10):773–88.doi:10.1002/bdra.20079.PMID 15472921.
  4. ^Augustine-Rauch KA, Zhang QJ, Leonard JL, Chadderton A, Welsh MJ, Rami HK, et al. (October 2004). "Evidence for a molecular mechanism of teratogenicity of SB-236057, a 5-HT1B receptor inverse agonist that alters axial formation".Birth Defects Research. Part A, Clinical and Molecular Teratology.70 (10):789–807.doi:10.1002/bdra.20076.PMID 15472891.
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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