Open Access Articles- Top Results for Dexfenfluramine


Systematic (IUPAC) name
Clinical data
MedlinePlus a682088
Pharmacokinetic data
Protein binding 36%
Half-life 17–20 hours
3239-44-9 7pxY
PubChem CID 66265
DrugBank DB01191 7pxY
ChemSpider 59646 7pxY
UNII E35R3G56OV 7pxY
KEGG D07805 7pxY
ChEBI CHEBI:439329 7pxY
ChEMBL CHEMBL248702 7pxY
Chemical data
Formula C12H16F3N
231.257 g/mol
 14pxY (what is this?)  (verify)

Dexfenfluramine, marketed as dexfenfluramine hydrochloride under the name Redux, is a serotonergic anorectic drug: it reduces appetite by increasing the amount of extracellular serotonin in the brain. It is the d-enantiomer of fenfluramine and is structurally similar to amphetamine, but lacks any psychologically stimulating effects.

Dexfenfluramine was for some years in the mid-1990s approved by the United States Food and Drug Administration for the purposes of weight loss. However, following multiple concerns about the cardiovascular side-effects of the drug, such approval was withdrawn and it was retired from the market in 1997. After it was removed in the US, dexfenfluramine was also pulled out in other global markets. It was later superseded by sibutramine, which, although initially considered a safer alternative to both dexfenfluramine and fenfluramine[citation needed], was likewise removed from the US market in 2010.[1]

The drug was manufactured by Interneuron Pharmaceuticals, a company co-founded by Richard Wurtman, aimed at marketing discoveries by Massachusetts Institute of Technology scientists.[2] In the case of Redux, Interneuron's manufacture was under licence to Wyeth-Ayerst Laboratories.[3] Although at the time of its release, some optimism prevailed that it might herald a new approach[citation needed], there remained some reservations amongst neurologists, twenty-two of whom petitioned the FDA to delay approval[citation needed]. Their concern was based on the work of George A. Ricaurte, whose techniques and conclusions were later questioned.[4]

In actuality, most conversant with the discussion felt that dexfenfuramine's only advantage was patent protection for its licensed companies. Racemic fenfluramine was far cheaper.

See also


  1. ^  Missing or empty |title= (help)[dead link]
  2. ^ Lemonick, Michael D; Dowell, William; Nash, J. Madeleine; Ramirez, Ainissa; Reid, Brian; Ressner, Jeffrey (23 September 1996), ., ed., "The New Miracle Drug?", Time, retrieved 3 October 2010  |chapter= ignored (help)
  3. ^ Lemonick, Michael D; Nash, J. Madeleine; Park, Alice; Thompson, Dick (29 September 1997), ., ed., "The Mood Molecule", Time, retrieved 4 October 2010  |chapter= ignored (help)
  4. ^ "DEA Accedes to Ecstasy Test". Wired. 2 March 2004. 

External links