Leuprorelin
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Non-proprietary name | Leuprorelin | |||||||||||||||||||||
other names |
5-Oxo-Pro-His-Trp-Ser-Tyr-d-Leu-Leu-Arg-Pro-NH-C2H5 |
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Molecular formula | C 59 H 84 N 16 O 12 | |||||||||||||||||||||
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Molar mass | 1209.40 g · mol -1 | |||||||||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Leuprorelin is a GnRH analog that stops hormone production and is used to artificially lower testosterone or estrogen levels in the blood. It is a peptide made up of nine amino acids .
indication
Leuprorelin is used among other things at
- the treatment of fibroids of the uterus ,
- the therapy of breast cancer ,
- Endometriosis ,
- the therapy of metastatic prostate cancer ,
- early onset of puberty ( pubertas praecox ) in girls and boys,
- Sex drive offenders due to the inhibition of sex hormone production.
- Cluster headache
Others
Leuprorelin is subject to a prescription in Germany. When protected from light and stored below 25 ° C, two-chamber syringes have a shelf life of 36 months. The application interval for monthly deposits may not exceed 32 days. Takeda achieved net sales of around EUR 8 billion with leuprorelin products in the 2012 financial year.
Trade names
Enantone (D, A), Trenantone (D, A), Sixantone (D, A), Lucrin (CH), various generics (D, CH)
Individual evidence
- ↑ Data sheet Leuprolide acetate salt from Sigma-Aldrich , accessed on May 29, 2011 ( PDF ).
- ↑ Entry on leuprorelin in the ChemIDplus database of the United States National Library of Medicine (NLM) .
- ↑ GenScript catalog ( Memento of 17 October 2006 at the Internet Archive ), accessed on June 13 of 2007.
- ↑ Hartmut Göbel: Cluster headache and other trigemino-autonomic headache disorders . In: The headache . Springer Berlin Heidelberg, Berlin, Heidelberg 2012, ISBN 978-3-642-20694-8 , pp. 497-538 , doi : 10.1007 / 978-3-642-20695-5_9 ( springer.com [accessed October 22, 2019]).
- ^ Takeda Pharmaceutical Company Limited .