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2) °ú¹Î¹ÝÀÀ : ¹ß¿ ¶§¶§·Î ¹ßÁø, ¾Ë·¹¸£±â¼º ÇǺιÝÀÀ, ¸Æ°üºÎÁ¾ µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·¯ÇÑ Áõ»óÀÌ ³ªÅ¸³ª´Â °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇÑ´Ù.
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5) ¼Òȱâ°è : ¶§¶§·Î ½Ä¿åºÎÁø, ±¸¿ª, ±¸Åä, À§ºÎºÒÄè°¨(¼ÒȺҷ®), À§Åë, º¹Åë, º¹ºÎÆØ¸¸°¨, ¼³»ç(¶§¶§·Î ÃâÇ÷À» µ¿¹Ý),À§¸·¼º´ëÀå¿°, ¹±Àº º¯ µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù. µå¹°°Ô ÃâÇ÷¼º ´ëÀå¿° µîÀÇ Ç÷º¯À» µ¿¹ÝÇÏ´Â ÁßÁõÀÇ ´ëÀå¿°ÀÌ ³ªÅ¸³ª´Â °æ¿ì°¡ ÀÖÀ¸¹Ç·Î º¹Åë, ºó¹øÇÑ ¼³»ç°¡ ÀÖ´Â °æ¿ì¿¡´Â Áï½Ã Åõ¿©¸¦ ÁßÁöÇÏ´Â µî ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù. ÃéÀå¿° Áõ»óÀÌ º¸°íµÈ ¹Ù ÀÖÀ¸³ª ´ëºÎºÐÀÇ È¯ÀÚ´Â ÃéÀå¿°ÀÌ ÀÌ»ó¹ÝÀÀÀ¸·Î ¾Ë·ÁÁø ¾à¹°À» º´¿ëÇÏ¿´´Ù.
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10) ÇǺΠ: ´ÙÇüÈ«¹Ý, ÀÚ¹ÝÁõ, ½ºÆ¼ºì½º-Á¸½¼ ÁõÈıº, µ¶¼ºÇ¥ÇDZ«»ç¿ëÇØ¿¡ À̸£´Â ÇǺιÝÀÀÀº µå¹°°Ô ³ªÅ¸³¯ ¼ö ÀÖ´Ù. ½ÃÆÇ ÈÄ Á¶»ç¿¡¼ ±Þ¼ºÀü½Å¼º¹ßÁø¼º³óÆ÷ÁõÀÌ º¸°íµÇ¾ú´Ù.
11) °¨¿° : ´Ù¸¥ Ç×»ýÁ¦¿¡¼¿Í ¸¶Âù°¡Áö·Î, ÀÌ ¾à »ç¿ë ½Ã ƯÈ÷ Àå±â°£ Åõ¿©ÇÏ´Â °æ¿ì ºñ°¨¼ö¼º º´¿ø±ÕÀÇ °úÀ×¼ºÀåÀ¸·Î ÀÎÇÑ Áߺ¹°¨¿°À» ÀÏÀ¸Å³ ¼ö ÀÖÀ¸¹Ç·Î ȯÀÚÀÇ »óŸ¦ Áö¼ÓÀûÀ¸·Î Æò°¡ÇÏ´Â °ÍÀÌ ÇÊ¿äÇÏ´Ù. Ä¡·á Áß Áߺ¹°¨¿°ÀÌ ³ªÅ¸³ª¸é ÀûÀýÇÑ Á¶Ä¡¸¦ ÃëÇØ¾ß ÇÑ´Ù.
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¡®¸¸¼ºÈ£Èí±âÁúȯ¿¡ Àú¿ë·® Àå±â Åõ¿©(low-dose, long-term therapy)µÈ macrolides°è¿ Á¦Á¦ÀÇ ÀÓ»óÀû À¯¿ë¼º ¹× ¾ÈÀü¼ºÀ» ÀÔÁõÇÒ ¸¸ÇÑ ±Ù°Å´Â ÇöÀç±îÁö ÃæºÐÇÏÁö ¾Ê´Ù°í ÆÇ´ÜµÈ´Ù.¡¯´Â EBH º¸°í¼¸¦ ÂüÁ¶½Ã Â÷ÈÄ macrolides°è Á¦Á¦ÀÇ Àú¿ë·® Àå±â Åõ¿©·Î ÀÎÇÑ ³»¼º±Õ ÃâÇöÀ̳ª ±Õ±³´ëÇö»ó µî ¾ÈÀü¼º ¹× À¯È¿¼º¿¡ ´ëÇÑ ÃæºÐÇÑ ±Ù°Å°¡ È®¸³µÉ ¶§±îÁö ¸¸¼ºÈ£Èí±âÁúȯ¿¡ macrolides°è¿ Á¦Á¦ÀÇ Àú¿ë·® Àå±âÅõ¿©´Â ÇöÇà´ë·Î ½Ä¾àû Çã°¡»çÇ×(¿ë¹ý¿ë·®) µîÀ» ÃʰúÇÑ °æ¿ì·Î º¸¾Æ ÀÎÁ¤ÇÏÁö ¾Æ´ÏÇÔ.
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[mizolastine]
[pimozide]
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[Roxithromycin] [Roxithromycin] CAS number /80214-83-1 ATC code /J01 FA06 PubChem /444037 DrugBank /APRD01305 Formula /C 41 H 76 N 2 O 15 Mol. mass /837.047 g/mol Bioavailability / ? Metabolism /Liver Excretion / ? Pregnancy cat. /
? (USA ) B1 (Aus ) Legal status /Routes / ?
Mechanism of Action
Roxithromycin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Roxithromycin prevents bacteria from growing, by interfering with their protein synthesis. Roxithromycin binds to the subunit 50S of the bacterial ribosome, and thus inhibits the translocation of peptides. Roxithromycin has similar antimicrobial spectrum as erythromycin, but is more effective against certain gram-negative bacteria, particularly Legionella pneumophila .
Pharmacology
Roxithromycin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Roxithromycin is a semi-synthetic macrolide antibiotic. It is very similar in composition, chemical structure and mechanism of action to erythromycin, azithromycin, or clarithromycin. Roxithromycin has the following antibacterial spectrum in vitro : Streptococcus agalactiae , Streptococcus pneumoniae (Pneumococcus), Neisseria meningitides (Meningococcus), Listeria monocytogenes , Mycoplasma pneumoniae , Chlamydia trachomatis , Ureaplasma urealyticum , Legionella pneumophila , Helicobacter (Campylobacter), Gardnerella vaginalis , Bordetella pertussis , Moraxella catarrhalis (Branhamella Catarrhalis ), and Haemophilus ducreyi . Roxithromycin is highly concentrated in polymorphonuclear leukocytes and macrophages, achieving intracellular concentrations greater than those outside the cell. Roxithromycin enhances the adhesive and chemotactic functions of these cells which in the presence of infection produce phagocytosis and bacterial lysis. Roxithromycin also possesses intracellular bactericidal activity.
Metabolism
Roxithromycin¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4)
Protein Binding
Roxithromycin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 96%, mainly to alpha1-acid glycoproteins
Half-life
Roxithromycin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 12 hours
Absorption
Roxithromycin¿¡ ´ëÇÑ Absorption Á¤º¸ Very rapidly absorbed and diffused into most tissues and phagocytes.
Pharmacokinetics
RoxithromycinÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
Èí¼ö : °æ±¸ : ºü¸£°Ô Èí¼öµÈ´Ù.
»ýü³»ÀÌ¿ë·ü : À½½Ä¹°¿¡ ÀÇÇØ 21%±îÁö °¨¼ÒÇÑ´Ù.
ºÐÆ÷ :
ºÐÆ÷¿ëÀû : 0.43-0.44 L/kg
ÅÂ¹Ý Åë°ú : ½Å»ý¾Æ¿¡¼ÀÇ ³óµµ°¡ ¸ðü ³óµµÀÇ 30-40% Á¤µµ
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´Ü¹é°áÇÕ : 85-95%°¡ ¥á1 -acid glycoprotein°ú °áÇÕ
´ë»ç : °£´ë»ç
¹Ý°¨±â :
¼Ò¾Æ : 19-21 ½Ã°£
¼ºÀÎ : 12 ½Ã°£
Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : °æ±¸ : 1-2 ½Ã°£, À½½Ä¹°¿¡ ÀÇÇØ Áö¿¬µÈ´Ù.
¼Ò½Ç :
10% Á¤µµ°¡ ¹Ìº¯Èü·Î ½Å¹è¼³µÈ´Ù.
53%°¡ º¯¹è¼³ µÈ´Ù.
Renal clearance´Â 6 mL/minÀ̰í, nonrenal clearance´Â 43 mL/min ÀÌ´Ù.
Biotransformation
Roxithromycin¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic. Roxithromycin is only partially metabolised, more than half the parent compound being excreted unchanged. Three metabolites have been identified in urine and faeces: the major metabolite is descladinose roxithromycin, with N-mono and N-di-demethyl roxithromycin as minor metabolites. The respective percentage of roxithromycin and these three metabolites is similar in urine and faeces.
Toxicity
Roxithromycin¿¡ ´ëÇÑ Toxicity Á¤º¸ Most common side-effects are gastrointestinal; diarrhoea, nausea, abdominal pain and vomiting. Less common side-effects include headaches, rashes, abnormal liver function values and alteration in senses of smell and taste.
Drug Interactions
Roxithromycin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Drug Target
[Drug Target]
Description
Roxithromycin¿¡ ´ëÇÑ Description Á¤º¸ Roxithromycin is a semi-synthetic macrolide antibiotic. It is very similar in composition, chemical structure and mechanism of action to erythromycin, azithromycin, or clarithromycin. Roxithromycin prevents bacteria from growing, by interfering with their protein synthesis. Roxithromycin binds to the subunit 50S of the bacterial ribosome, and thus inhibits the translocation of peptides. Roxithromycin has similar antimicrobial spectrum as erythromycin, but is more effective against certain gram-negative bacteria, particularly Legionella pneumophila. It can treat respiratory tract, urinary and soft tissue infections.
Drug Category
Roxithromycin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial Agents
Smiles String Canonical
Roxithromycin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)(O)CC(C)C(=NOCOCCOC)C(C)C(O)C1(C)O
Smiles String Isomeric
Roxithromycin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@](C)(O)C[C@@H](C)\C(=N\OCOCCOC)C(C)[C@@H](O)[C@]1(C)O
InChI Identifier
Roxithromycin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C41H76N2O15/c1-15-29-41(10,49)34(45)24(4)31(42-53-21-52-17-16-50-13)22(2)19-39(8,48)36(58-38-32(44)28(43(11)12)18-23(3)54-38)25(5)33(26(6)37(47)56-29)57-30-20-40(9,51-14)35(46)27(7)55-30/h22-30,32-36,38,44-46,48-49H,15-21H2,1-14H3/t22-,23-,24+,25+,26-,27+,28+,29-,30+,32-,33+,34-,35+,36-,38+,39-,40-,41-/m1/s1
Chemical IUPAC Name
Roxithromycin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (3R,4S,5S,6R,7R,9R,11S,12R,13S,14R)-6-[(2S,3R,4S,6R)-4-dimethylamino-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-4-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-10-(2-methoxyethoxymethoxyimino)-3,5,7,9,11,13-hexamethyl-1-oxacyclotetradecan-2-one
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