Fluprednisolone
Fluprednisolone
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Names |
IUPAC name
(6S,8S,9S,10R,11S,13S,14S,17R)-6-fluoro-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one |
Identifiers |
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53-34-9 Y |
ChEMBL |
ChEMBL1200774 N |
Jmol-3D images |
Image |
KEGG |
D04227 Y |
PubChem |
5876 |
C[C@]12C[C@@H]([C@H]3[C@H]([C@@H]1CC[C@@]2(C(=O)CO)O)C[C@@H](C4=CC(=O)C=C[C@]34C)F)O
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Properties |
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C21H27FO5 |
Molar mass |
378.43 g/mol |
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) |
N verify (what is: Y/N?) |
Infobox references |
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Fluprednisolone is a pregnane. It is a corticosteroid.[1]
References
- ↑ Naggar VF, Gouda MW, Khalil SA (December 1977). "In vitro adsorption of some corticosteroids on antacids". Pharmazie 32 (12): 778–81. PMID 613316.
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| Synthesis modifiers | |
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| Description |
- Glands
- Hormones
- thyroid
- mineralocorticoids
- Physiology
- Development
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| Disease |
- Diabetes
- Congenital
- Neoplasms and cancer
- Other
- Symptoms and signs
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| Treatment |
- Procedures
- Drugs
- calcium balance
- corticosteroids
- oral hypoglycemics
- pituitary and hypothalamic
- thyroid
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| Receptor | |
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| Enzyme | |
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| Others | |
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| See also: Androgenics • Estrogenics • Mineralocorticoidics • Progestogenics |
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