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Mechanism of Action
Triamcinolone¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ The antiinflammatory actions of corticosteroids are thought to involve lipocortins, phospholipase A2 inhibitory proteins which, through inhibition of arachidonic acid, control the biosynthesis of prostaglandins and leukotrienes. The immune system is suppressed by corticosteroids due to a decrease in the function of the lymphatic system, a reduction in immunoglobulin and complement concentrations, the precipitation of lymphocytopenia, and interference with antigen-antibody binding.
Pharmacology
Triamcinolone¿¡ ´ëÇÑ Pharmacology Á¤º¸ Triamcinolone and its derivatives are synthetic glucocorticoids that are used for their antiinflammatory or immunosuppressive properties.
Metabolism
Triamcinolone¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
Protein Binding
Triamcinolone¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 68%
Half-life
Triamcinolone¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 88 minutes
Absorption
Triamcinolone¿¡ ´ëÇÑ Absorption Á¤º¸ Rapid absorption following oral administration
Pharmacokinetics
Triamcinolone acetonideÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
ÀÛ¿ëÁö¼Ó½Ã°£ : °æ±¸ : 8¡12½Ã°£
Èí¼ö : ¿Ü¿ëÁ¦ : Àü½ÅÀûÀ¸·Î Èí¼öµÉ ¼öµµ ÀÖ´Ù.
ÃÖ´ëÈ¿°ú ¹ßÇö½Ã°£ : ±ÙÀ°ÁÖ»ç : 8¡10½Ã°£ À̳»
»ý¸®Àû ¹Ý°¨±â : 18¡36½Ã°£
Biotransformation
Triamcinolone¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic.
Toxicity
Triamcinolone¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50 =>500mg/kg (in rats)
Drug Interactions
Triamcinolone¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Food Interaction
Triamcinolone¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available
Drug Target
[Drug Target]
Description
Triamcinolone¿¡ ´ëÇÑ Description Á¤º¸ 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)
Drug Category
Triamcinolone¿¡ ´ëÇÑ Drug_Category Á¤º¸ Adrenergic AgentsAnti-inflammatory AgentsGlucocorticoids
Smiles String Canonical
Triamcinolone¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC12CC(O)C3(F)C(CCC4=CC(=O)C=CC34C)C1CC(O)C2(O)C(=O)CO
Smiles String Isomeric
Triamcinolone¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@]12C[C@H](O)[C@@]3(F)[C@@H](CCC4=CC(=O)C=C[C@]34C)[C@@H]1C[C@@H](O)[C@]2(O)C(=O)CO
InChI Identifier
Triamcinolone¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C21H27FO6/c1-18-6-5-12(24)7-11(18)3-4-13-14-8-15(25)21(28,17(27)10-23)19(14,2)9-16(26)20(13,18)22/h5-7,13-16,23,25-26,28H,3-4,8-10H2,1-2H3/t13-,14-,15+,16-,18-,19-,20-,21-/m0/s1
Chemical IUPAC Name
Triamcinolone¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (8S,9R,10S,11S,13S,14S,16R,17S)-9-fluoro-11,16,17-trihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one
Drug-Induced Toxicity Related Proteins
TRIAMCINOLONE ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein :Serotransferrin Drug :triamcinolone Toxicity :stimulate growth of NEL-M1 human melanoma cells . [¹Ù·Î°¡±â] Replated Protein :InsulinDrug :triamcinolone Toxicity :stimulate growth of NEL-M1 human melanoma cells . [¹Ù·Î°¡±â]
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