Fludrocortisone
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General | ||||||||||||||||||||||
Non-proprietary name | Fludrocortisone | |||||||||||||||||||||
other names |
(8 S , 9 R , 10 S , 11 S , 13 S , 14 S , 17 R ) -9-fluoro-11,17-dihydroxy-17- (2-hydroxyacetyl) -10,13-dimethyl-1,2 , 6,7,8,11,12,14,15,16-decahydrocyclopenta [ a ] phenanthren-3-one |
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Molecular formula | C 21 H 29 FO 5 | |||||||||||||||||||||
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properties | ||||||||||||||||||||||
Molar mass | 380.45 g · mol -1 | |||||||||||||||||||||
Physical state |
firmly |
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Melting point |
225 ° C |
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Fludrocortisone is a synthetic aldosterone derivative whose effects are primarily mineralocorticoid , but also have a low glucocorticoid effect. It is used to treat primary adrenal insufficiency ( Addison's disease , congenital adrenal hyperplasia ).
Mechanism of action
The effects of fludrocortisone mainly come about through binding to mineralocorticoid receptors . Thus, in the renal reabsorption of sodium and - chloride - ions increased. In addition, the renal excretion of potassium , hydrogen and ammonium ions is increased. In addition, the glomerular filtration rate is also increased in the glomeruli . In addition, the water permeability of the distal tubules is reduced.
Pharmacokinetics
The active ingredient is by oral rapidly absorbed recording. The maximum plasma concentration is reached in humans after four to eight hours. Fludrocortisone is hydrolyzed in the liver and 80% is excreted through the kidneys and 20% with the stool. The plasma half-life is approximately 3.5 hours. The effects last for 12 to 36 hours.
Trade names
- Florinef , Astonin-H
Web links
- Entry on fludrocortisone at Vetpharm
Individual evidence
- ↑ a b c Entry on fludrocortisone at Vetpharm, accessed on May 25, 2017.
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.