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| Related FDA Approved Drug |
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µå·°ÀÎÆ÷ ÀǾàǰ ¿ä¾à/»ó¼¼Á¤º¸
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 FDA : Cµî±Þ
(clobetasol; )
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»ó±â ÀÓºÎÅõ¿©¿¡ ´ëÇÑ Á¤º¸´Â Àü»êó¸® µÇ¸é¼ ÀÔ·Â ¿À·ù °¡´É¼ºÀÌ Á¸ÀçÇÕ´Ï´Ù. ¿À·ù °¡´É¼ºÀ» ÃÖ¼ÒÈÇϱâ À§ÇÏ¿© ¸¹Àº ³ë·ÂÀ» ±â¿ïÀ̰í ÀÖÀ¸³ª, ±× Á¤È®¼º¿¡ ´ëÇÏ¿© È®½ÅÀ» µå¸± ¼ö ¾ø½À´Ï´Ù. ÀÌ¿¡ ´ëÇØ ȸ»ç´Â Ã¥ÀÓÀ» ÁöÁö ¾Ê½À´Ï´Ù.
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¹Ýµå½Ã °ø½Å·Â ÀÖ´Â ¹®ÇåÀ» ´Ù½Ã Çѹø Âü°í ÇϽñ⠹ٶó¸ç ÀÇ»ç ¶Ç´Â ¾à»çÀÇ ÆÇ´Ü¿¡ µû¶ó Åõ¿©¿©ºÎ°¡ °áÁ¤µÇ¾î¾ß ÇÕ´Ï´Ù.
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| Pharmacokinetics |
À¯·áÁ¤º¸ÀÔ´Ï´Ù.
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º´¿ë±Ý±â :
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| Mechanism of Action |
Clobetasol¿¡ ´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.
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| Pharmacology |
Clobetasol¿¡ ´ëÇÑ Pharmacology Á¤º¸ Like other topical corticosteroids, clobetasol has anti-inflammatory, antipruritic, and vasoconstrictive properties. It is a very high potency 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.
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| Metabolism |
Clobetasol¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
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| Absorption |
Clobetasol¿¡ ´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.
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| Pharmacokinetics |
Clobetasol PropionateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : °æÇÇÈí¼ö´Â Á¦Á¦¿¡ ÇÔÀ¯µÈ ÷°¡Á¦, ÇǺΠ»óÅÂ, ¿ë·®, ºÀÇÕ¿ä¹ýÀÇ »ç¿ë ¿©ºÎ µî ¸¹Àº ¿ä¼Ò¿¡ ¿µÇâÀ» ¹ÞÀ¸¸ç, °æÇÇ Èí¼öÀ²Àº ´Ù¾çÇÔ.
- ¼Ò½Ç : ´¢ ¹× ´ãÁóÀ¸·Î ¹è¼³µÊ
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| Toxicity |
Clobetasol¿¡ ´ëÇÑ Toxicity Á¤º¸ Oral LD50 in rat and mouse is >3000 mg/kg. Topically applied clobetasol 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).
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| Drug Interactions |
Clobetasol¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Clobetasol¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available
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| Drug Target |
[Drug Target]
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| Description |
Clobetasol¿¡ ´ëÇÑ Description Á¤º¸ A derivative of prednisolone with high glucocorticoid activity and low mineralocorticoid activity. Absorbed through the skin faster than fluocinonide, it is used topically in treatment of psoriasis but may cause marked adrenocortical suppression. [PubChem]
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| Drug Category |
Clobetasol¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-inflammatory AgentsCorticosteroids, topicalGlucocorticoids
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| Smiles String Canonical |
Clobetasol¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCC(=O)OC1(C(C)CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC12C)C(=O)CCl
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| Smiles String Isomeric |
Clobetasol¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CCC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CCl
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| InChI Identifier |
Clobetasol¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C25H32ClFO5/c1-5-21(31)32-25(20(30)13-26)14(2)10-18-17-7-6-15-11-16(28)8-9-22(15,3)24(17,27)19(29)12-23(18,25)4/h8-9,11,14,17-19,29H,5-7,10,12-13H2,1-4H3/t14-,17-,18-,19-,22-,23-,24-,25-/m0/s1
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| Chemical IUPAC Name |
Clobetasol¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ [(8S,9R,10S,11S,13S,14S,16S,17R)-17-(2-chloroacetyl)-9-fluoro-11-hydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl] propanoate
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