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Fluocortin

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Chemical compound Pharmaceutical compound
Fluocortin
Clinical data
Other names6α-fluoro-11β,21-dihydroxy-16α-methylpregna-1,4-diene-3,20,21-trione
ATC code
Pharmacokinetic data
Bioavailability80% i.v.
Elimination half-life1.3 hr.
Identifiers
IUPAC name
  • 2-phenanthren-17-yl]-2-oxoacetic acid
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
CompTox Dashboard (EPA)
ECHA InfoCard100.046.698 Edit this at Wikidata
Chemical and physical data
FormulaC22H27FO5
Molar mass390.451 g·mol
3D model (JSmol)
SMILES
  • C1C23C(C4=CC(=O)C=C4(3(C2(1C(=O)C(=O)O)C)O)C)F
InChI
  • InChI=1S/C22H27FO5/c1-10-6-13-12-8-15(23)14-7-11(24)4-5-21(14,2)18(12)16(25)9-22(13,3)17(10)19(26)20(27)28/h4-5,7,10,12-13,15-18,25H,6,8-9H2,1-3H3,(H,27,28)/t10-,12+,13+,15+,16+,17-,18-,21+,22+/m1/s1
  • Key:PUWHHWCHAVXSIG-NCLPIGKXSA-N
  (verify)

Fluocortin is a corticosteroid. It is similar to fluocortolone, but with one more carbonyl group.

References

  1. Täuber U, Haack D, Nieuweboer B, Kloss G, Vecsei P, Wendt H (January 1984). "The pharmacokinetics of fluocortolone and prednisolone after intravenous and oral administration". International Journal of Clinical Pharmacology, Therapy, and Toxicology. 22 (1): 48–55. PMID 6698661.
Glucocorticoids and antiglucocorticoids (D07, H02)
Glucocorticoids
Natural
Synthetic
Antiglucocorticoids
Synthesis modifiers
See also
Glucocorticoid receptor modulators
Mineralocorticoids and antimineralocorticoids
List of corticosteroids
Glucocorticoid receptor modulators
GRTooltip Glucocorticoid receptor
Agonists
Mixed
(SEGRMsTooltip Selective glucocorticoid receptor agonists)
Antagonists
Others
See also
Receptor/signaling modulators
Glucocorticoids and antiglucocorticoids
Mineralocorticoid receptor modulators
List of corticosteroids
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