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SIB-1553A

From Wikipedia, the free encyclopedia
SIB-1553A
Names
Preferred IUPAC name
4-{[2-(1-Methylpyrrolidin-2-yl)ethyl]sulfanyl}phenol
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
UNII
  • InChI=1S/C13H19NOS/c1-14-9-2-3-11(14)8-10-16-13-6-4-12(15)5-7-13/h4-7,11,15H,2-3,8-10H2,1H3
    Key: NVZGJSVPOOILDI-UHFFFAOYSA-N
  • InChI=1/C13H19NOS/c1-14-9-2-3-11(14)8-10-16-13-6-4-12(15)5-7-13/h4-7,11,15H,2-3,8-10H2,1H3
    Key: NVZGJSVPOOILDI-UHFFFAOYAV
  • OC1=CC=C(SCCC2CCCN2C)C=C1
Properties
C13H19NOS
Molar mass237.36 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

SIB-1553A is anicotinic acetylcholine receptoragonist that is selective for receptors with aβ4 subunit. Administration of SIB-1553A improved memory and attention in aParkinson's disease model.[1]

References

[edit]
  1. ^Schneider, JS (July 2003). "The Subtype-Selective Nicotinic Acetylcholine Receptor Agonist SIB-1553A Improves Both Attention and Memory Components of a Spatial Working Memory Task in Chronic Low Dose 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine-Treated Monkeys".Journal of Pharmacology and Experimental Therapeutics.306 (1):401–6.doi:10.1124/jpet.103.051912.PMID 12721323.S2CID 7060934.
nAChRsTooltip Nicotinic acetylcholine receptors
Agonists
(andPAMsTooltip positive allosteric modulators)
Antagonists
(andNAMsTooltip negative allosteric modulators)
Precursors
(andprodrugs)


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