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Related FDA Approved Drug
±âÁØ ¼ººÐ:
FLUOROMETHOLONE FLAREX (FLUOROMETHOLONE ACETATE)
FLUOR-OP (FLUOROMETHOLONE)
FML (FLUOROMETHOLONE)
FML FORTE (FLUOROMETHOLONE)
FML-S (FLUOROMETHOLONE; SULFACETAMIDE SODIUM)
OXYLONE (FLUOROMETHOLONE)
TOBRASONE (FLUOROMETHOLONE ACETATE; TOBRAMYCIN)
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FDA : Cµî±Þ
(fluorometholone opthalmic )
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Mechanism of Action
Fluorometholone¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ There is no generally accepted explanation for the mechanism of action of ocular corticosteroids. However, corticosteroids are thought to act by the induction of phospholipase A2 inhibitory proteins, collectively called lipocortins. It is postulated that these proteins control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes by inhibiting the release of their common precursor, arachidonic acid. Arachidonic acid is released from membrane phospholipids by phospholipase A2.
Pharmacology
Fluorometholone¿¡ ´ëÇÑ Pharmacology Á¤º¸ Corticosteroids such as fluorometholone inhibit the inflammatory response to a variety of inciting agents and probably delay or slow healing. They inhibit the edema, fibrin deposition, capillary dilation, leukocyte migration, capillary proliferation, fibroblast proliferation, deposition of collagen, and scar formation associated with inflammation.
Metabolism
Fluorometholone¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4)
Protein Binding
Fluorometholone¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
Half-life
Fluorometholone¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Not Available
Absorption
Fluorometholone¿¡ ´ëÇÑ Absorption Á¤º¸ Not Available
Pharmacokinetics
FluorometholoneÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
Èí¼ö : ´ëºÎºÐÀº ¹æ¼ö(aqueous humor)·Î Èí¼öµÇ°í ¼Ò·®ÀÌ Àü½ÅÈí¼ö µÈ´Ù.
Biotransformation
Fluorometholone¿¡ ´ëÇÑ Biotransformation Á¤º¸ Not Available
Toxicity
Fluorometholone¿¡ ´ëÇÑ Toxicity Á¤º¸ Side effects may include acute anterior uveitis and perforation of the globe. Keratitis, conjunctivitis, corneal ulcers, mydriasis, conjunctival hyperemia, loss of accommodation and ptosis have occasionally been reported following local use of corticosteroids. LD50 = 234 mg/kg (rats)
Drug Interactions
Fluorometholone¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Drug Target
[Drug Target]
Description
Fluorometholone¿¡ ´ëÇÑ Description Á¤º¸ A glucocorticoid employed, usually as eye drops, in the treatment of allergic and inflammatory conditions of the eye. It has also been used topically in the treatment of various skin disorders. (From Martindale, The Extra Pharmacopoeia, 30th ed, p732)
Dosage Form
Fluorometholone¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Solution / drops OphthalmicSuspension Ophthalmic
Drug Category
Fluorometholone¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Allergic AgentsAnti-inflammatory AgentsGlucocorticoids
Smiles String Canonical
Fluorometholone¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC1CC2C3CCC(O)(C(C)=O)C3(C)CC(O)C2(F)C2(C)C=CC(=O)C=C12
Smiles String Isomeric
Fluorometholone¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@H]1C[C@H]2[C@@H]3CC[C@](O)(C(C)=O)[C@@]3(C)C[C@H](O)[C@]2(F)[C@@]2(C)C=CC(=O)C=C12
InChI Identifier
Fluorometholone¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C22H29FO4/c1-12-9-17-15-6-8-21(27,13(2)24)20(15,4)11-18(26)22(17,23)19(3)7-5-14(25)10-16(12)19/h5,7,10,12,15,17-18,26-27H,6,8-9,11H2,1-4H3/t12-,15-,17-,18-,19-,20-,21-,22-/m0/s1
Chemical IUPAC Name
Fluorometholone¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (6S,8S,9R,10S,11S,13S,14S,17R)-17-acetyl-9-fluoro-11,17-dihydroxy-6,10,13-trimethyl-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one
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