Estramustine
Structural formula | ||||||||||||||||||||||
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Non-proprietary name | Estramustine | |||||||||||||||||||||
other names |
17 β -hydroxyestra-1,3,5 (10) -trien-3-yl- N , N -bis (2-chloroethyl) carbamate |
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Molecular formula | C 23 H 31 Cl 2 NO 3 | |||||||||||||||||||||
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properties | ||||||||||||||||||||||
Molar mass | 440.40 g · mol -1 | |||||||||||||||||||||
Physical state |
firmly |
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Melting point |
104-105 ° C |
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safety instructions | ||||||||||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Estramustine (trade name: Estracyt, among others, manufactured by Pharmacia , etc.) is a cytostatic agent , in the structurally combining an alkylating agent ( alkylating agents , nitrogen mustard derivative) and estrogen ( estradiol ) is present (dual mechanism of action).
pharmacology
application
It is used in the secondary treatment of advanced prostate cancer .
Side effects
As with other cytostatics, the side effects are mainly derived from the inhibitory effects on rapidly dividing body cells:
- Gastrointestinal disorders
- Edema
- Heart failure
- Thromboembolism
- Libido and potency loss
- Changes in blood count
- Liver damage
Trade names
Cellmustin (D), EstraCept (D), Estracyt (D, A, CH), Medactin (D), Multosin (D) and a generic (D)
See also
Carmustine , nimustine , lomustine
Individual evidence
- ^ The Merck Index . An Encyclopaedia of Chemicals, Drugs and Biologicals . 14th edition, 2006, pp. 635-636, ISBN 978-0-911910-00-1 .
- ↑ harmonized classification for this substance . A labeling of estramustine in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), retrieved on February 7, 2020, is reproduced from a self-classification by the distributor . There is not yet a
- ↑ Red List, as of August 2009.
- ↑ AM comp. d. Switzerland, as of August 2009.
- ↑ AGES-PharmMed, as of August 2009.