Çöó¼ÕÅ©¸²(µðÇ÷ζó¼Õ¾Æ¼¼Å×ÀÌÆ®) 500g Flrasone Cream
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(2020.02.04)
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057000804\0 ¿ø/500g/º´(2024.11.01) (ÇöÀç¾à°¡) \61,500 ¿ø/500g/º´(2020.05.01)(º¯°æÀü¾à°¡)
ATCÄÚµå
Diflorasone / D07AC10
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Related FDA Approved Drug
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FDA : Cµî±Þ
(diflorasone diacetate topical )
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Pharmacokinetics
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Mechanism of Action
Diflorasone¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ The precise mechanism of the antiinflammatory activity of topical steroids in the treatment of steroid-responsive dermatoses, in general, is uncertain. 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
Diflorasone¿¡ ´ëÇÑ Pharmacology Á¤º¸ Like other topical corticosteroids, diflorasone has anti-inflammatory, antipruritic, and vasoconstrictive properties. Once absorbed through the skin, topical corticosteroids are handled through pharmacokinetic pathways similar to systemically administered corticosteroids. Diflorasone is a potent topical corticosteroid that should not be used with occlusive dressings. It is recommended that treatment should be limited to 2 consecutive weeks and therapy should be discontinued when adequate results have been achieved.
Metabolism
Diflorasone¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
Protein Binding
Diflorasone¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Bound to plasma proteins in varying degrees.
Half-life
Diflorasone¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Not Available
Absorption
Diflorasone¿¡ ´ëÇÑ Absorption Á¤º¸ Topical corticosteroids can be absorbed from intact healthy skin. The extent of percutaneous absorption of topical corticosteroids is determined by many factors, including the vehicle and the integrity of the epidermal barrier. Occlusion, inflammation and/or other disease processes in the skin may also increase percutaneous absorption.
Pharmacokinetics
Diflorasone DiacetateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
Èí¼ö : ±¹¼Ò Àû¿ë½Ã Èí¼ö´Â °ÅÀÇ µÇÁö ¾ÊÀ¸¸ç ¾à 1% Á¤µµ°¡ Àü½Å ¼øÈ¯À¸·Î Èí¼öµÇ°í, ¹ÐºÀÇÏ´Â °æ¿ì °æÇÇÈí¼ö°¡ Áõ°¡µÈ´Ù.
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Biotransformation
Diflorasone¿¡ ´ëÇÑ Biotransformation Á¤º¸ Metabolized, primarily in the liver, and then excreted by the kidneys.
Toxicity
Diflorasone¿¡ ´ëÇÑ Toxicity Á¤º¸ Topically applied diflorasone can be absorbed in sufficient amounts to produce systemic effects. Symptoms of overdose include thinning of skin and suppression of adrenal cortex (decreased ability to respond to stress).
Drug Interactions
Diflorasone¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Food Interaction
Diflorasone¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available
Drug Target
[Drug Target]
Description
Diflorasone¿¡ ´ëÇÑ Description Á¤º¸ Diflorasone is a corticosteroid.
Drug Category
Diflorasone¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-inflammatory AgentsGlucocorticoids
Smiles String Canonical
Diflorasone¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC1CC2C3CC(F)C4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(OC(C)=O)C(=O)COC(C)=O
Smiles String Isomeric
Diflorasone¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@H]1C[C@H]2[C@@H]3C[C@H](F)C4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(C)=O)C(=O)COC(C)=O
InChI Identifier
Diflorasone¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C26H32F2O7/c1-13-8-17-18-10-20(27)19-9-16(31)6-7-23(19,4)25(18,28)21(32)11-24(17,5)26(13,35-15(3)30)22(33)12-34-14(2)29/h6-7,9,13,17-18,20-21,32H,8,10-12H2,1-5H3/t13-,17-,18-,20-,21-,23-,24-,25-,26-/m0/s1
Chemical IUPAC Name
Diflorasone¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ [(6S,8S,9R,10S,11S,13S,14S,16S,17R)-17-(2-acetyloxyacetyl)-6,9-difluoro-11-hydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl] acetate
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