Autor: |
Linli He, Melanie Marguerit, Roger P. Bakale, Shawn P. Allwein, Jason Rossi, James J. Reif, Yi Wang, Renee C. Roemmele, Gill Little |
Rok vydání: |
2015 |
Předmět: |
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Zdroj: |
European Journal of Organic Chemistry. 2015:8003-8010 |
ISSN: |
1434-193X |
DOI: |
10.1002/ejoc.201500906 |
Popis: |
A total synthesis of enantiomerically pure [14C]-labelled (–)-homoharringtonine in 17 steps is reported. This synthetic process enabled the production of Good Manufacturing Practice (GMP) compliant (–)-[14C]homoharringtonine that was used in a human mass balance study that was a post-approval commitment to the U.S. Food and Drug Administration. (–)-Homoharringtonine, also called omacetaxine mepesuccinate, is approved to treat adult patients with chronic myeloid leukemia (CML), a blood and bone marrow disease. In November 2012, the product was commercialised as Synribo® in the U.S., marketed by Teva Pharmaceuticals. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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