Substance

ID:503

Names and Identifiers
IUPAC name
(1R,2S,10S,11S,13R,14S,15S,17S)-1-fluoro-13,14,17-trihydroxy-14-(2-hydroxyacetyl)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,6-dien-5-one
IUPAC Traditional name
triamcinolone
Synonyms
TriamcinoloneFluoxyprednisoloneFluoxiprednisoloneTriamcinolonum [INN]Triamcinolone hexacetonideTiamcinolonum [INN-Latin]TriamcinaloneTriamcinolone acetonideTriamcinolone diacetateTriamcinolona [INN-Spanish]
Brand Name
KenalogAdcortylAristocortAristocort AAristogelDelphicortFlutexOrionSk-TriamcinoloneTriamcetTriatexTristojectAristospanCinolone-TNasacortNasacort HfaOmcilonOraloneTriamcinolonTridermAristocort TabletsKenalog-40LedercortNasacort AqRodinoloneTriacortTriam-TablinenCelesteCinoloneKenacortKenacort-AKenacort-AgTriamcinlonVetalogVolonTriloneAzmacortKenalog-10OmicilonPolcortolonTriacetVolon AFougeraKenalog in OrabaseKenalog-HOracortTri-NasalTricortaleTrymex
Registration numbers
PubChem CID
PubChem SID
CAS Number
Properties
Physical Property
Hydrophobicity(logP)
0.2
Solubility
80 mg/L
Molecule Details
Drug Groups
approved
Description
A glucocorticoid given, as the free alcohol or in esterified form, orally, intramuscularly, by local injection, by inhalation, or applied topically in the management of various disorders in which corticosteroids are indicated. (From Martindale, The Extra Pharmacopoeia, 30th ed, p739)
Indication
For the treatment of perennial and seasonal allergic rhinitis.
Pharmacology
Triamcinolone and its derivatives are synthetic glucocorticoids that are used for their antiinflammatory or immunosuppressive properties.
Toxicity
LD50=>500mg/kg (in rats)
Affected Organisms
Humans and other mammals
Biotransformation
Hepatic.
Absorption
Rapid absorption following oral administration
Half Life
88 minutes
Protein Binding
68%
Molecular Spectra
No Data Available
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References
No Data Available
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