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       Ofloxacin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Ofloxacin acts on DNA gyrase, an enzyme which, like human topoisomerase, prevents the excessive supercoiling of DNA during replication or transcription. 
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       Ofloxacin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Ofloxacin is a quinolone/fluoroquinolone antibiotic. Ofloxacin is bactericidal and its mode of action depends on blocking of bacterial DNA replication by binding itself to an enzyme called DNA gyrase, which allows the untwisting required to replicate one DNA double helix into two. Notably the drug has 100 times higher affinity for bacterial DNA gyrase than for mammalian. Ofloxacin is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria. 
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       Ofloxacin¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 1A2 (CYP1A2) 
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       Ofloxacin¿¡ ´ëÇÑ Absorption Á¤º¸ Bioavailability of ofloxacin in the tablet formulation is approximately 98% 
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       Ofloxacin¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50=5450 mg/kg (orally in mice) 
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    | Drug Interactions | 
    
       Ofloxacin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Aluminium	Formation of non-absorbable complexesBismuth	Formation of non-absorbable complexesCalcium	Formation of non-absorbable complexesIron	Formation of non-absorbable complexesMagnesium oxide	Formation of non-absorbable complexesMagnesium	Formation of non-absorbable complexesSucralfate	Formation of non-absorbable complexesZinc	Formation of non-absorbable complexesWarfarin	The quinolone increases the anticoagulant effectAcenocoumarol	The quinolone increases the anticoagulant effectDicumarol	The quinolone increases the anticoagulant effectAnisindione	The quinolone increases the anticoagulant effectDihydroquinidine barbiturate	Increased risk of cardiotoxicity and arrhythmiasQuinidine	Increased risk of cardiotoxicity and arrhythmiasQuinidine barbiturate	Increased risk of cardiotoxicity and arrhythmiasFoscarnet	Increased risk of convulsionsProcainamide	The quinolone increases the effect of procainamide 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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       Ofloxacin¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take without regard to meals.Avoid high doses of caffeine. 
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      [Drug Target]
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    | Description | 
    
       Ofloxacin¿¡ ´ëÇÑ Description Á¤º¸ A synthetic fluoroquinolone (fluoroquinolones) antibacterial agent that inhibits the supercoiling activity of bacterial DNA gyrase, halting DNA replication. [PubChem] 
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    | Dosage Form | 
    
       Ofloxacin¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Liquid	OphthalmicSolution	OphthalmicTablet	Oral 
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    | Drug Category | 
    
       Ofloxacin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsAnti-Infective Agents, UrinaryAnti-InfectivesNucleic Acid Synthesis InhibitorsQuinolones 
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    | Smiles String Canonical | 
    
       Ofloxacin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC1COC2=C3N1C=C(C(O)=O)C(=O)C3=CC(F)=C2N1CCN(C)CC1 
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    | Smiles String Isomeric | 
    
       Ofloxacin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@H]1COC2=C3N1C=C(C(O)=O)C(=O)C3=CC(F)=C2N1CCN(C)CC1 
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    | InChI Identifier | 
    
       Ofloxacin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C18H20FN3O4/c1-10-9-26-17-14-11(16(23)12(18(24)25)8-22(10)14)7-13(19)15(17)21-5-3-20(2)4-6-21/h7-8,10H,3-6,9H2,1-2H3,(H,24,25)/f/h24H 
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    | Chemical IUPAC Name | 
    
       Ofloxacin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (+/-)-9-fluoro-2, 3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[1, 2, 3-de]-1, 4-benzoxazine-6-carboxylic acid 
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                          ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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