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MS-245

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
MS-245
Clinical data
ATC code
  • none
Identifiers
  • 2-[5-methoxy-1-(phenylsulfonyl)-1H-indol-3-yl]-N,N-dimethylethanamine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC19H22N2O3S
Molar mass358.46 g·mol−1
3D model (JSmol)
  • COc2cc1c(CCN(C)C)cn(c1cc2)S(=O)(=O)c3ccccc3
  • InChI=1S/C19H22N2O3S/c1-20(2)12-11-15-14-21(19-10-9-16(24-3)13-18(15)19)25(22,23)17-7-5-4-6-8-17/h4-10,13-14H,11-12H2,1-3H3
  • Key:AIJIQCBYMBZLJD-UHFFFAOYSA-N
  (verify)

MS-245 is atryptamine derivative used inscientific research. It acts as aselective5-HT6 receptorantagonist with aKi of 2.3 nM, and was derived throughstructure-activity relationship development of the selective 5-HT6 agonistEMDT.[1] It has been used as alead compound for further development of tryptamine-derived 5-HT6 antagonists.[2][3] In animal studies it has been shown to boost the activity of, but not substitute for, bothamphetamine andnicotine.[4][5]

See also

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References

[edit]
  1. ^Tsai Y, Dukat M, Slassi A, MacLean N, Demchyshyn L, Savage JE, et al. (October 2000). "N1-(Benzenesulfonyl)tryptamines as novel 5-HT6 antagonists".Bioorganic & Medicinal Chemistry Letters.10 (20):2295–9.doi:10.1016/S0960-894X(00)00453-4.PMID 11055342.
  2. ^Abate C, Kolanos R, Dukat M, Setola V,Roth BL, Glennon RA (August 2005). "Interaction of chiral MS-245 analogs at h5-HT6 receptors".Bioorganic & Medicinal Chemistry Letters.15 (15):3510–3.doi:10.1016/j.bmcl.2005.05.092.PMID 15990303.
  3. ^Dukat M, Mosier PD, Kolanos R, Roth BL, Glennon RA (February 2008)."Binding of serotonin and N1-benzenesulfonyltryptamine-related analogs at human 5-HT6 serotonin receptors: receptor modeling studies".Journal of Medicinal Chemistry.51 (3):603–11.doi:10.1021/jm070910s.PMC 5994921.PMID 18201064.
  4. ^Pullagurla M, Bondareva T, Young R, Glennon RA (June 2004). "Modulation of the stimulus effects of (+)amphetamine by the 5-HT6 antagonist MS-245".Pharmacology, Biochemistry, and Behavior.78 (2):263–8.doi:10.1016/j.pbb.2004.03.017.PMID 15219766.S2CID 25350474.
  5. ^Young R, Bondareva T, Wesolowska A, Young S, Glennon RA (September 2006). "Effect of the 5-HT(6) serotonin antagonist MS-245 on the actions of (-)nicotine".Pharmacology, Biochemistry, and Behavior.85 (1):170–7.doi:10.1016/j.pbb.2006.07.029.PMID 16950502.S2CID 38662192.
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
Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
Cyclized tryptamines
Isotryptamines
Related compounds
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