Tarenflurbil

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Structural formula
Structural formula of Tarenflurbil
General
Non-proprietary name Tarenflurbil
other names
  • ( R ) -2- (3-fluoro-4-phenylphenyl) propionic acid ( IUPAC )
  • ( R ) -2-flurbiprofen
Molecular formula C 15 H 13 FO 2
External identifiers / databases
CAS number 51543-40-9
EC number 257-264-7
ECHA InfoCard 100.052.041
PubChem 92337
ChemSpider 83361
DrugBank DB05289
Wikidata Q849769
Drug information
Drug class

Non-opioid analgesics

properties
Molar mass 244.26 g · mol -1
safety instructions
GHS labeling of hazardous substances
06 - Toxic or very toxic

danger

H and P phrases H: 301
P: 301 + 310
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Tarenflurbil , a non-steroidal anti- inflammatory drug (NSAID), is the eutomer and dextrorotatory enantiomer of flurbiprofen - a racemate .

Tarenflurbil is an active ingredient of the production of beta-amyloid - protein 42 via inhibition of (Abeta) enzyme gamma secretase cuts. When it was taken, a phase III study showed that patients had more Abeta with 38 instead of 42 amino acids. Since the brain can further metabolize these proteins, there are hopes that it can influence the basic process of the formation of plaques specific to Alzheimer's disease. As an effect, the 800 mg per day dosage slowed the gradual deterioration in activities of daily living observed over two years in the mild form of Alzheimer's disease . On the other hand, no significant influence could be seen in the cognitive tests.

See also

Individual evidence

  1. a b Data sheet (R) - (-) - 2-Fluoro-α-methyl-4-biphenylacetic acid from Sigma-Aldrich , accessed on April 23, 2011 ( PDF ).
  2. Beher D, Clarke EE, Wrigley JD, et al. : Selected non-steroidal anti-inflammatory drugs and their derivatives target gamma-secretase at a novel site. Evidence for an allosteric mechanism . In: J. Biol. Chem. . 279, No. 42, October 2004, pp. 43419-26. doi : 10.1074 / jbc.M404937200 . PMID 15304503 .
  3. ^ According to the British Alzheimer's Society , news from May 2, 2008.

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