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| DUR (ÀǾàǰ»ç¿ëÆò°¡) |
º´¿ë±Ý±â :
°í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
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| Mechanism of Action |
Beclomethasone¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Unbound corticosteroids cross cell membranes and bind with high affinity to specific cytoplasmic receptors. The result includes inhibition of leukocyte infiltration at the site of inflammation, interference in the function of mediators of inflammatory response, suppression of humoral immune responses, and reduction in edema or scar tissue. The antiinflammatory actions of corticosteroids are thought to involve phospholipase A2 inhibitory proteins, lipocortins, which control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes.
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| Pharmacology |
Beclomethasone¿¡ ´ëÇÑ Pharmacology Á¤º¸ Beclomethasone, a synthetic halogenated glucocorticoid with antiinflammatory and vasoconstrictive effects, is used for treating steroid-dependent asthma, allergic or nonallergic rhinitis, or recurrent nasal polyps.
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| Metabolism |
Beclomethasone¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
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| Protein Binding |
Beclomethasone¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 87% to albumin and transcortin
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| Half-life |
Beclomethasone¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 2.8 hours
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| Absorption |
Beclomethasone¿¡ ´ëÇÑ Absorption Á¤º¸ Mean peak plasma concentration was 88pg/ml at 0.5 hour
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| Pharmacokinetics |
Beclomethasone DipropionateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Ä¡·á È¿°ú : »ç¿ëÇÑÁö 1¡4ÁÖ ³»¿¡ ¹ßÇö
- ÈíÀÔ(inhalation)
- Èí¼ö : ½±°Ô Èí¼öµÈ´Ù. Èí¼öµÇ±â Àü¿¡ ÆóÀÇ esterases¿¡ ÀÇÇØ ºü¸£°Ô °¡¼öºÐÇØµÈ´Ù.
- ºÐÆ÷ : Åõ¿©·®ÀÇ 10¡25%°¡ ±âµµ¿¡ µµ´Þ
- °æ±¸
- Èí¼ö : 90%
- ºÐÆ÷ : À¯ÁóÀ¸·Î ºÐºñµÈ´Ù.
- ´Ü¹é°áÇÕ : 87%
- ´ë»ç : °£¿¡¼ ´ë»çµÈ´Ù.
- ¹Ý°¨±â : Ãʱ⠹ݰ¨±â : 3½Ã°£, ¸»±â(terminal) ¹Ý°¨±â : 15½Ã°£
- ¼Ò½Ç : ½Å¹è¼³
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| Biotransformation |
Beclomethasone¿¡ ´ëÇÑ Biotransformation Á¤º¸ Metabolism mediated via esterase enzymes that are found in most tissues. Undergoes rapid and extensive conversion to beclomenthasone-17-monopropionate (17-BMP) during absorption
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| Toxicity |
Beclomethasone¿¡ ´ëÇÑ Toxicity Á¤º¸ The acute toxicity of beclomethasone dipropionate is low. The only harmful effect that follows inhalation of large amounts of the drug over a short period of time is suppression of hypothalamic-pituitary-adrenal (HPA) function. Chronic: The excessive use of beclomethasone dipropionate over a long period could lead to adrenal suppression.
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| Drug Interactions |
Beclomethasone¿¡ ´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 |
Beclomethasone¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available
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| Drug Target |
[Drug Target]
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| Description |
Beclomethasone¿¡ ´ëÇÑ Description Á¤º¸ An anti-inflammatory, synthetic glucocorticoid. It is used topically as an anti-inflammatory agent and in aerosol form for the treatment of asthma. [PubChem]
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| Drug Category |
Beclomethasone¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Asthmatic AgentsAnti-inflammatory AgentsAntiarrhythmic AgentsCorticosteroidsGlucocorticoids
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| Smiles String Canonical |
Beclomethasone¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC1CC2C3CCC4=CC(=O)C=CC4(C)C3(Cl)C(O)CC2(C)C1(O)C(=O)CO
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| Smiles String Isomeric |
Beclomethasone¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(Cl)[C@@H](O)C[C@]2(C)[C@@]1(O)C(=O)CO
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| InChI Identifier |
Beclomethasone¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C22H29ClO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,12,15-17,24,26,28H,4-5,8,10-11H2,1-3H3/t12-,15-,16-,17-,19-,20-,21-,22-/m0/s1
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| Chemical IUPAC Name |
Beclomethasone¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (8S,9R,10S,11S,13S,14S,16S,17R)-9-chloro-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one
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ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2023-12-02
-
º» ¼öÁ¤ÀÏ Á¤º¸´Â Çã°¡Á¤º¸ ÀÌ¿ÜÀÇ ±âŸÁ¤º¸ ¼öÁ¤ÀÏÀ» ÀǹÌÇϹǷÎ, Çã°¡Á¤º¸¼öÁ¤ÀÏÀº º»¹®¿¡ Ç¥±âµÈ ³¯Â¥¸¦ ÂüÁ¶ÇϽñ⠹ٶø´Ï´Ù.
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»ó¼¼Á¤º¸´Â ½ÄǰÀǾàǰ¾ÈÀüóÀÇ Á¦Ç°Çã°¡»çÇ×À» Åä´ë·Î ÀÛ¼ºµÇ¾úÀ¸¸ç ¿ä¾àÁ¤º¸´Â »ó¼¼Á¤º¸ ¹× ±âŸ¹®ÇåÀ» ±â¹ÝÀ¸·Î µå·°ÀÎÆ÷¿¡¼ ÆíÁýÇÑ ³»¿ëÀÔ´Ï´Ù. Á¦Ç°Çã°¡»çÇ×ÀÇ ¸ñÂ÷¿Í ´Ù¼Ò »óÀÌÇÒ ¼ö ÀÖ½À´Ï´Ù. |
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µå·°ÀÎÆ÷ ÀǾàÇмúÁ¤º¸´Â ½ÄǰÀǾàǰ¾ÈÀüóÀÇ Á¦Ç°Çã°¡»çÇ×, Çмú¹®Çå, Á¦¾àȸ»ç Á¦°øÁ¤º¸ µîÀ» ±Ù°Å·Î ÀÛ¼ºµÈ Âü°í Á¤º¸ÀÔ´Ï´Ù.
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
Ã¥ÀÓÀ» ÁöÁö ¾Ê½À´Ï´Ù. ÀÚ¼¼ÇÑ ³»¿ëÀº ¡°Ã¥ÀÓÀÇ ÇÑ°è ¹× ¹ýÀû°íÁö¡±¸¦ ÂüÁ¶ÇØ ÁֽʽÿÀ.
¹Ýµå½Ã Á¦Á¶¡¤¼öÀÔ»ç, ÆÇ¸Å»ç, ÀÇ»ç, ¾à»ç¿¡°Ô ÃÖÁ¾ÀûÀ¸·Î È®ÀÎÇϽñ⠹ٶø´Ï´Ù.
ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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