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                    ¹Ì³ëŬ¸°Ä¡°ú¿ë¿¬°í(¿°»ê¹Ì³ë»çÀÌŬ¸°)  MINOCLINE ORAL OINT[Minocycline HCl]  
                    
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Porphyromonas ginglvalis, 
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    | Mechanism of Action | 
    
       Minocycline¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Minocycline passes directly through the lipid bilayer or passively diffuses through porin channels in the bacterial membrane. Tetracyclines like minocycline bind to the 30S ribosomal subunit, preventing the binding of tRNA to the mRNA-ribosome complex and interfering with protein synthesis. 
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    | Pharmacology | 
     
       Minocycline¿¡ ´ëÇÑ Pharmacology Á¤º¸ Minocycline, the most lipid soluble and most active tetracycline antibiotic, is, like doxycycline, a long-acting tetracycline. Minocycline's effects are related to the inhibition of protein synthesis. Although minocycline's broader spectrum of activity, compared to other members of the group, includes activity against Neisseria meningitidis, its use as a prophylaxis is no longer recomended because of side effects (dizziness and vertigo). Current research is examining the possible neuroprotective effects of minocycline against progression of Huntington's Disease, an inherited neurodegenerative disorder. The neuroprotective action of minocycline may include its inhibitory effect on 5-lipoxygenase, an inflammatory enzyme associated with brain aging. 
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    | Absorption | 
    
       Minocycline¿¡ ´ëÇÑ Absorption Á¤º¸ Rapidly absorbed from the gastrointestinal tract and absorption is not significantly impaired by ingestion of food or milk. Oral bioavailability is 100%. 
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    | Pharmacokinetics | 
    
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    | Toxicity | 
    
       Minocycline¿¡ ´ëÇÑ Toxicity Á¤º¸ Minocycline has been observed to cause a dark discoloration of the thyroid in experimental animals (rats, minipigs, dogs and monkeys). In the rat, chronic treatment with minocycline has resulted in goiter accompanied by elevated radioactive iodine uptake and evidence of thyroid tumor production. Minocycline has also been found to produce thyroid hyperplasia in rats and dogs. LD50=2380 mg/kg (rat, oral), LD50=3600 mg/kg (mouse, oral) 
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    | Drug Interactions | 
    
       Minocycline¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Acitretin	Increased risk of intracranial hypertensionAluminium	Formation of non-absorbable complexesAmoxicillin	Possible antagonism of actionAmpicillin	Possible antagonism of actionAzlocillin	Possible antagonism of actionAztreonam	Possible antagonism of actionBacampicillin	Possible antagonism of actionCarbenicillin	Possible antagonism of actionClavulanate	Possible antagonism of actionCloxacillin	Possible antagonism of actionCyclacillin	Possible antagonism of actionDicloxacillin	Possible antagonism of actionFlucloxacillin	Possible antagonism of actionHetacillin	Possible antagonism of actionMethicillin Acyl-Serine	Possible antagonism of actionMezlocillin	Possible antagonism of actionNafcillin	Possible antagonism of actionOxacillin	Possible antagonism of actionPenicillin G	Possible antagonism of actionPenicillin V	Possible antagonism of actionPiperacillin	Possible antagonism of actionPivampicillin	Possible antagonism of actionPivmecillinam	Possible antagonism of actionTazobactam	Possible antagonism of actionTicarcillin	Possible antagonism of actionZinc	Formation of non-absorbable complexesTrisalicylate-choline	Formation of non-absorbable complexesMagnesium oxide	Formation of non-absorbable complexesMagnesium	Formation of non-absorbable complexesSalicylate-magnesium	Formation of non-absorbable complexesIron	Formation of non-absorbable complexesBismuth	Formation of non-absorbable complexesCalcium	Formation of non-absorbable complexesAttapulgite	Formation of non-absorbable complexesBismuth Subsalicylate	Formation of non-absorbable complexesAnisindione	The tetracycline increases the anticoagulant effectAcenocoumarol	The tetracycline increases the anticoagulant effectDicumarol	The tetracycline increases the anticoagulant effectWarfarin	The tetracycline increases the anticoagulant effectDigoxin	The tetracycline increases the effect of digoxin in 10% of patientsInsulin	The tetracycline increases the risk of hypoglycemiaMethoxyflurane	The tetracycline increases the renal toxicity of methoxyfluraneEthinyl Estradiol	This anti-infectious agent could decrease the effect of the oral contraceptiveMestranol	This anti-infectious agent could decrease the effect of the oral contraceptiveEtretinate	Increased risk of intracranial hypertensionIsotretinoin	This anti-infectious agent could decrease the effect of the oral contraceptive 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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    | Drug Target | 
    
      
      [Drug Target]
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    | Description | 
    
       Minocycline¿¡ ´ëÇÑ Description Á¤º¸ A tetracycline analog, having a 7-dimethylamino and lacking the 5 methyl and hydroxyl groups, which is effective against tetracycline-resistant staphylococcus infections. [PubChem] 
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    | Dosage Form | 
    
       Minocycline¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule	Oral 
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    | Drug Category | 
    
       Minocycline¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsTetracyclines 
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    | Smiles String Canonical | 
    
       Minocycline¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CN(C)C1C2CC3CC4=C(C=CC(O)=C4C(O)=C3C(=O)C2(O)C(=O)C(C1=O)=C(N)O)N(C)C 
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    | Smiles String Isomeric | 
    
       Minocycline¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CN(C)[C@H]1[C@@H]2C[C@@H]3CC4=C(C=CC(O)=C4C(O)=C3C(=O)[C@]2(O)C(=O)\C(C1=O)=C(/N)O)N(C)C 
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    | InChI Identifier | 
    
       Minocycline¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C23H27N3O7/c1-25(2)12-5-6-13(27)15-10(12)7-9-8-11-17(26(3)4)19(29)16(22(24)32)21(31)23(11,33)20(30)14(9)18(15)28/h5-6,9,11,17,27-28,32-33H,7-8,24H2,1-4H3/b22-16+/t9-,11-,17-,23-/m0/s1 
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    | Chemical IUPAC Name | 
    
       Minocycline¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (2Z,4S,4aS,5aR,12aS)-2-(amino-hydroxymethylidene)-4,7-bis(dimethylamino)-10,11,12a-trihydroxy-4a,5,5a,6-tetrahydro-4H-tetracene-1,3,12-trione 
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                ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2025-07-25
              
 
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                º» ¼öÁ¤ÀÏ Á¤º¸´Â Çã°¡Á¤º¸ ÀÌ¿ÜÀÇ ±âŸÁ¤º¸ ¼öÁ¤ÀÏÀ» ÀǹÌÇϹǷÎ, Çã°¡Á¤º¸¼öÁ¤ÀÏÀº º»¹®¿¡ Ç¥±âµÈ ³¯Â¥¸¦ ÂüÁ¶ÇϽñ⠹ٶø´Ï´Ù.
                
              
     
             
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                          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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