eliglustat
Sign in to saveAlso known as GENZ-112638, Genz-99067, Genz 99067, N-[(1R,2R)-1-(2,3-Dihydro-1,4-benzodioxin-6-yl)-1-hydroxy-3-(1-pyrrolidinyl)-2-propanyl]octanamide
Eliglustat, sold under the brand name Cerdelga, is a medication used for the treatment of Gaucher's disease. It was discovered at the University of Michigan, developed by Genzyme Corp, and was approved by the FDA in August 2014. Commonly used as the tartrate salt, the compound is believed to work by inhibition of glucosylceramide synthase. According to an article in Journal of the American Medical Association the oral substrate reduction therapy resulted in "significant improvements in spleen volume, hemoglobin level, liver volume, and platelet count" in untreated adults with Gaucher disease T
Research
182 papers- Eliglustat.2006
- Eliglustat.2012
- Eliglustat: first global approval.Drugs · 2014
- Eliglustat Therapy and CYP2D6 Genotype.2012
- Eliglustat: A Review in Gaucher Disease Type 1.Drugs · 2015
via PubMed
Wikidata facts
- Has part
- carbon
- Mass
- 404.267508
- Has use
- medication
Show 8 more facts
- medical condition treated
- Gaucher's disease
- chemical formula
- C₂₃H₃₆N₂O₄
- canonical SMILES
- CCCCCCCC(=O)NC(CN1CCCC1)C(C2=CC3=C(C=C2)OCCO3)O
- isomeric SMILES
- CCCCCCCC(=O)N[C@H](CN1CCCC1)[C@@H](C2=CC3=C(C=C2)OCCO3)O
- World Health Organisation international non-proprietary name
- eliglustat
- defined daily dose
- 0.168
- subject has role
- enzyme inhibitor
- significant drug interaction
- ketoconazole
via Wikidata · CC0
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Encyclopedic overview
4 sectionsContents
- History
- Society and culture
- Economics
- References
Eliglustat, sold under the brand name Cerdelga, is a medication used for the treatment of Gaucher's disease. It was discovered at the University of Michigan, developed by Genzyme Corp, and was approved by the FDA in August 2014. Commonly used as the tartrate salt, the compound is believed to work by inhibition of glucosylceramide synthase. According to an article in Journal of the American Medical Association the oral substrate reduction therapy resulted in "significant improvements in spleen volume, hemoglobin level, liver volume, and platelet count" in untreated adults with Gaucher disease Type 1.
==History== Norman Radin began exploring the possibility of inhibiting the synthesis of lipid substrates involved in Gaucher's disease as early as 1982, and, in collaboration with the laboratory of Jim Shayman, found several candidate inhibitors in the mid-1990s. Genzyme initially rejected the candidates developed by Radin and Shayman, but after a news broke of a competitor developing a new treatment for Gaucher's disease, licensed the Radin/Shayman patents in 2000. Eliglustat did not receive FDA approval for another 14 years, a delay that Shayman speculated was due to some company leaders not being fully committed to developing a drug that would compete with imiglucerase (brand name Cerezyme), Genzyme's flagship treatment for Gaucher's disease.
Excerpted from Wikipedia’s “eliglustat” article, available under the CC BY-SA 4.0 licence.