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| Mechanism of Action |
Mesalazine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Although the mechanism of action of mesalazine is not fully understood, it appears to be topical rather than systemic. Mucosal production of arachidonic acid metabolites, both through the cyclooxygenase pathways, i.e., prostanoids, and through the lipoxygenase pathways, i.e., leukotrienes and hydroxyeicosatetraenoic acids, is increased in patients with chronic inflammatory bowel disease, and it is possible that mesalamine diminishes inflammation by blocking cyclooxygenase and inhibiting prostaglandin production in the colon.
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| Pharmacology |
Mesalazine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Mesalazine (INN, BAN), also known as Mesalamine (USAN) or 5-aminosalicylic acid (5-ASA), is an anti-inflammatory drug used to treat inflammation of the digestive tract (Crohn's disease) and mild to moderate ulcerative colitis. Mesalazine is a bowel-specific aminosalicylate drug that is metabolized in the gut and has its predominant actions there, thereby having fewer systemic side effects. As a derivative of salicylic acid, 5-ASA is also an antioxidant that traps free radicals, which are potentially damaging by-products of metabolism.
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| Metabolism |
Mesalazine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
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| Absorption |
Mesalazine¿¡ ´ëÇÑ Absorption Á¤º¸ 20 to 30% absorbed following oral administration. 10 to 35% absorbed from the colon (rectal suppository) - extent of absorption is determined by the length of time the drug is retained in the colon.
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| Pharmacokinetics |
MesalazineÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : Á÷Àå³» Åõ¿© : ¾à 15%. ü·ù½Ã°£, º´Á¸ÇÏ´Â À§Àå°ü°è Áúȯ, ´ëÀåÀÇ pH¿¡ µû¶ó ´Ù¾çÇÏ´Ù.
- ´ë»ç : °£¿¡¼ acetyl-5-aminosalicylic acid (Ȱ¼ºÇü)·Î ¾Æ¼¼Æ¿ÈµÇ¾î glucuronide Æ÷ÇÕü·Î ´ë»çµÈ´Ù. Àå³» ´ë»çµµ ÀϾ ¼ö ÀÖ´Ù.
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- Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : 4-7 ½Ã°£ À̳»
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| Toxicity |
Mesalazine¿¡ ´ëÇÑ Toxicity Á¤º¸ Oral, mouse: LD50 = 3370 mg/kg; Oral, rat: LD50 = 2800 mg/kg; Skin, rabbit: LD50 = >5 gm/kg. There have been no documented reports of serious toxicity in man resulting from massive overdosing with mesalamine. Under ordinary circumstances, mesalamine absorption from the colon is limited.
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| Drug Interactions |
Mesalazine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Azathioprine The 5-ASA derivative increases the toxicity of thiopurineMercaptopurine The 5-ASA derivative increases the toxicity of thiopurineThioguanine The 5-ASA derivative increases the toxicity of thiopurine
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Mesalazine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take without regard to meals.
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| Drug Target |
[Drug Target]
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| Description |
Mesalazine¿¡ ´ëÇÑ Description Á¤º¸ An anti-inflammatory agent, structurally related to the salicylates, which is active in inflammatory bowel disease. It is considered to be the active moiety of sulphasalazine. (From Martindale, The Extra Pharmacopoeia, 30th ed)
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| Dosage Form |
Mesalazine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Enema RectalSuppository RectalSuspension RectalTablet, coated OralTablet, delayed release OralTablet, extended release Oral
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| Drug Category |
Mesalazine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Inflammatory Agents, Non-Steroidal
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| Smiles String Canonical |
Mesalazine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ NC1=CC(C(O)=O)=C(O)C=C1
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| Smiles String Isomeric |
Mesalazine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ NC1=CC(C(O)=O)=C(O)C=C1
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| InChI Identifier |
Mesalazine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C7H7NO3/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,9H,8H2,(H,10,11)/f/h10H
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| Chemical IUPAC Name |
Mesalazine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 5-amino-2-hydroxybenzoic 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
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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