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ÀßÄÚÆ®Ä°¼¿ SALCOAT CAPSULE[Beclomethasone Dipropionate]
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Àü¹®ÀǾàǰ | ºñ±Þ¿©
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644703290[B06500021]
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[Drugbank ÀÇ ¼ººÐÁ¤º¸¿¶÷] [Beclomethasone]
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| Related FDA Approved Drug |
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µå·°ÀÎÆ÷ ÀǾàǰ ¿ä¾à/»ó¼¼Á¤º¸
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| Brandname Á¤º¸ |
Beclomethasone
Brand Names/Synonyms
- Aerobec
- Aldecin
- Anceron
- Andion
- Beclacin
- Becloforte
- Beclomet
- Beclometasona [Inn-Spanish]
- Beclometasondipropionat Mikron
- Beclometasondipropionat Mikron.
- Beclometasone
- Beclometasonum [Inn-Latin]
- Beclorhinol
- Becloval
- Beclovent
- Becodisks
- Beconase
- Beconase AQ
- Beconasol
- Becotide
- Clenil-A
- Entyderma
- Inalone
- Korbutone
- Propaderm
- Qvar
- Qvar 80
- Rino-Clenil
- Sanasthmax
- Sanasthmyl
- Vancenase
- Vancenase AQ
- Vanceril
- Vanceril Double Strength
- Viarex
- Viarox
Brand Name Mixturesnone
Chemical IUPAC Name[9-chloro-11-hydroxy-10,13,16-trimethyl-3-oxo-17-(2-propanoyloxyacetyl)-6,7,8,11,12, 14,15,16-octahydrocyclopenta[a]phenanthren-17-yl] propanoate
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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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| Dosage Form |
Beclomethasone¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Aerosol, metered NasalAerosol, metered Respiratory (inhalation)Cream TopicalSpray NasalSuspension Nasal
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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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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
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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The database contains the following fields: The generic name of each chemical For module A10 (liver enzyme composite module): Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the number of active and marginally active scores for each compound at the five individual endpoints (see research article for full description of method) Number of endpoints at which each compound is marginally active (M) Number of endpoints at which each compound is active (A) For modules A11 to A15 (alkaline phosphatase increased, SGOT increased, SGPT increased, LDH increased, and GGT increased, respectively): Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the RI and ADR values (see the research article for full description of method) Number of ADR reports for each compound, given as <4 or ¡Ã4 Reporting Index value for each compound, except where no shipping units were available (NSU) Group 1 comprises of compounds for which ADR data were available for the first five years of marketing, so when no ADR reports were listed during this period the compounds were evaluated as inactive. Group 2 comprises of compounds for which a 'steady state' period of ADR data were available (1992-1996). In cases where no ADR reports were filed during this period, the compounds were scored as 'NA' (data not available) since they may have had one or more ADR reports during their first five years of marketing which should not be negated by a lack of ADR reports during the steady-state period. BECLOMETHASONE[GGT Increase][Composite Activity](Score) I(Marginal) 0(Active) 0[Alkaline Phosphatase Increase](Activity Score) I(Number of Rpts) <4(Index value) 0[SGOT Increase](Activity Score) I(Number of Rpts) <4(Index value) 0[SGPT Increase](Activity Score) I(Number of Rpts) <4(Index value) 0[LDH Increase](Activity Score) I(Number of Rpts) <4(Index value) 0[GGT Increase](Activity Score) I(Number of Rpts) <4(Index value) 0
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