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| Mechanism of Action |
Flurbiprofen¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ The antiinflammatory effect of flurbiprofen may result from the reversible inhibition of cyclooxygenase, causing the peripheral inhibition of prostaglandin synthesis. Flurbiprofen also inhibits the migration of leukocytes into sites of inflammation and prevents the formation of thromboxane A2, an aggregating agent, by the platelets.
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| Pharmacology |
Flurbiprofen¿¡ ´ëÇÑ Pharmacology Á¤º¸ Flurbiprofen, a nonsteroidal antiinflammatory drug (NSAID) of the propionic acid class, is used for the relief of pain and inflammation associated with rheumatoid arthritis and osteoarthritis and for the inhibition of intraoperative miosis. Flurbiprofen exhibits antiinflammatory, analgesic, and antipyretic activities.
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| Metabolism |
Flurbiprofen¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 2C9 (CYP2C9)
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| Protein Binding |
Flurbiprofen¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ > 99%
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| Half-life |
Flurbiprofen¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 4.7-5.7 hours
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| Absorption |
Flurbiprofen¿¡ ´ëÇÑ Absorption Á¤º¸ The mean oral bioavailability of flurbiprofen from tablets is 96% relative to an oral solution.
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| Pharmacokinetics |
FlurbiprofenÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
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| Biotransformation |
Flurbiprofen¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic. Cytochrome P450 2C9 plays an important role in the metabolism of flurbiprofen to its major metabolite, 4¡¯-hydroxy-flurbiprofen. The 4¡¯-hydroxy-flurbiprofen metabolite showed little anti-inflammatory activity in animal models of inflammation.
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| Toxicity |
Flurbiprofen¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50=10 mg/kg (orally in dogs).
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| Drug Interactions |
Flurbiprofen¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Alendronate Increased risk of gastric toxicityMethotrexate The NSAID increases the effect and toxicity of methotrexateAnisindione The NSAID increases the anticoagulant effectDicumarol The NSAID increases the anticoagulant effectAcenocoumarol The NSAID increases the anticoagulant effectWarfarin The NSAID increases the anticoagulant effectCyclosporine Monitor for nephrotoxicity
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Flurbiprofen¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take with food to reduce irritation.Avoid alcohol.
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| Drug Target |
[Drug Target]
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| Description |
Flurbiprofen¿¡ ´ëÇÑ Description Á¤º¸ An anti-inflammatory analgesic and antipyretic of the phenylalkynoic acid series. It has been shown to reduce bone resorption in periodontal disease by inhibiting carbonic anhydrase. [PubChem]
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| Dosage Form |
Flurbiprofen¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule, extended release OralLiquid OphthalmicTablet Oral
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| Drug Category |
Flurbiprofen¿¡ ´ëÇÑ Drug_Category Á¤º¸ AnalgesicsAnti-Inflammatory Agents, Non-SteroidalAnti-inflammatory AgentsCarbonic Anhydrase InhibitorsCyclooxygenase InhibitorsNonsteroidal Antiinflammatory Agents (NSAIDs)
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| Smiles String Canonical |
Flurbiprofen¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(C(O)=O)C1=CC(F)=C(C=C1)C1=CC=CC=C1
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| Smiles String Isomeric |
Flurbiprofen¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@@H](C(O)=O)C1=CC(F)=C(C=C1)C1=CC=CC=C1
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| InChI Identifier |
Flurbiprofen¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C15H13FO2/c1-10(15(17)18)12-7-8-13(14(16)9-12)11-5-3-2-4-6-11/h2-10H,1H3,(H,17,18)/f/h17H
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| Chemical IUPAC Name |
Flurbiprofen¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2-(3-fluoro-4-phenylphenyl)propanoic acid
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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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