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| Related FDA Approved Drug |
±âÁØ ¼ººÐ: TETRAHYDROZOLINE HYDROCHLORIDETYZINE (TETRAHYDROZOLINE HYDROCHLORIDE)
±âÁØ ¼ººÐ: FLUOROMETHOLONEFLAREX (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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| 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.
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| 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.
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| Metabolism |
Fluorometholone¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4)
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| Protein Binding |
Fluorometholone¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
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| Half-life |
Fluorometholone¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Not Available
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| Absorption |
Fluorometholone¿¡ ´ëÇÑ Absorption Á¤º¸ Not Available
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| Pharmacokinetics |
FluorometholoneÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : ´ëºÎºÐÀº ¹æ¼ö(aqueous humor)·Î Èí¼öµÇ°í ¼Ò·®ÀÌ Àü½ÅÈí¼ö µÈ´Ù.
Tetrahydrozoline HClÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ÃæÇ÷Á¦°ÅÈ¿°ú ¹ßÇö½Ã°£ : ºñ°³» Åõ¿© : 4-8 ½Ã°£ À̳»
- ÀÛ¿ëÁö¼Ó½Ã°£ : ¾ÈÇ÷°ü ¼öÃà : 2-3 ½Ã°£
- Èí¼ö : ±¹¼Ò : ¶§·Î Àü½Å Èí¼ö°¡ ³ªÅ¸³².
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| Biotransformation |
Fluorometholone¿¡ ´ëÇÑ Biotransformation Á¤º¸ Not Available
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| 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)
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| Drug Interactions |
Fluorometholone¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Drug Target |
[Drug Target]
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| 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)
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| Dosage Form |
Fluorometholone¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Solution / drops OphthalmicSuspension Ophthalmic
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| Drug Category |
Fluorometholone¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Allergic AgentsAnti-inflammatory AgentsGlucocorticoids
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| 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
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| 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
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| 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
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| 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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Á¤º¸ÀÇ Á¤È®¼ºÀ» À§ÇØ ³ë·ÂÇϰí ÀÖÀ¸³ª ÆíÁý»óÀÇ ¿À·ù, Çã°¡»çÇ× º¯°æ, Ãß°¡ÀûÀÎ Çмú¿¬±¸ ¶Ç´Â Àӻ󿬱¸ ¹ßÇ¥ µîÀ¸·Î ÀÎÇØ ¹ß»ýÇÏ´Â ¹®Á¦¿¡ ´ëÇØ µå·°ÀÎÆ÷´Â
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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