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½ì¶óÆ®ÇǶóÁø¾Æ¹ÌµåÁ¤250mg CELLART PYRAZINAMIDE TAB.250mg[Pyrazinamide]
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| Mechanism of Action |
Pyrazinamide¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Pyrazinamide is an important sterilizing drug that shortens tuberculosis (TB) therapy. However, the mechanism of action of pyrazinamide is poorly understood because of its unusual properties. In literature it has been written that the pyrazinoic acid (POA), the active moiety of pyrazinamide, disrupted membrane energetics and inhibited membrane transport function at acid pH in Mycobacterium tuberculosis. The antimycobacterial activity appears to partly depend on conversion of the drug to POA. Susceptible strains of M. tuberculosis produce pyrazinamidase, an enzyme that deaminates pyrazinamide to POA, and the vitro susceptibility of a given strain of the organism appears to correspond to its pyrazinamidase activity. Experimental evidence suggests that pyrazinamide diffuses into M. tuberculosis in a passive manner, is converted into POA by pyrazinamidase, and because of an inefficient efflux system, accumulates in huge amounts in the bacterial cytoplasm. The accumulation of POA lowers the intracellular pH to a suboptimal level that is likely to inactivate a vital target enzyme such as fatty acid synthase.
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| Pharmacology |
Pyrazinamide¿¡ ´ëÇÑ Pharmacology Á¤º¸ Pyrazinamide kills or stops the growth of certain bacteria that cause tuberculosis (TB). It is used with other drugs to treat tuberculosis. It is a highly specific agent and is active only against Mycobacterium tuberculosis. In vitro and in vivo, the drug is active only at a slightly acid pH.
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| Metabolism |
Pyrazinamide¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Xanthine dehydrogenase/oxidase
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| Protein Binding |
Pyrazinamide¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ ~10% (bound to plasma proteins)
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| Half-life |
Pyrazinamide¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 9-10 hours (normal conditions)
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| Absorption |
Pyrazinamide¿¡ ´ëÇÑ Absorption Á¤º¸ Rapidly and well absorbed from the gastrointestinal tract.
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| Pharmacokinetics |
PyrazinamideÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : °æ±¸ : Àß Èí¼öµÈ´Ù.
- ºÐÆ÷ : °£, Æó, ³úô¼ö¾×À» Æ÷ÇÔÇÑ Ã¼³» Á¶Á÷ ¹× ü¾×¿¡ ³Î¸® ºÐÆ÷
- ³ú¼ö¸·ÀÇ °¨¿°¿¡ °ü°è ¾øÀÌ MIC ÀÌ»óÀÇ ³óµµ·Î ³úô¼ö¾×¿¡ ºÐÆ÷
- ´Ü¹é°áÇÕ : 50%
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| Toxicity |
Pyrazinamide¿¡ ´ëÇÑ Toxicity Á¤º¸ Side effects include liver injury, arthralgias, anorexia, nausea and vomiting, dysuria,malaise and fever, sideroblastic anemia, adverse effects on the blood clotting mechanism or vascular integrity, and hypersensitivity reactions such as urticaria, pruritis and skin rashes.
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| Drug Interactions |
Pyrazinamide¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Cyclosporine Pyrazinamide decreases the effect of cyclosporine
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Pyrazinamide¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take without regard to meals.
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| Drug Target |
[Drug Target]
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| Description |
Pyrazinamide¿¡ ´ëÇÑ Description Á¤º¸ A pyrazine that is used therapeutically as an antitubercular agent. [PubChem]
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| Dosage Form |
Pyrazinamide¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Tablet Oral
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| Drug Category |
Pyrazinamide¿¡ ´ëÇÑ Drug_Category Á¤º¸ Antitubercular Agents
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| Smiles String Canonical |
Pyrazinamide¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ NC(=O)C1=NC=CN=C1
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| Smiles String Isomeric |
Pyrazinamide¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ NC(=O)C1=NC=CN=C1
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| InChI Identifier |
Pyrazinamide¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C5H5N3O/c6-5(9)4-3-7-1-2-8-4/h1-3H,(H2,6,9)/f/h6H2
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| Chemical IUPAC Name |
Pyrazinamide¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ pyrazine-2-carboxamide
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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