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³¹Ù¿Àݼ¿ NANBAO CAP.[±¤±¸½Å , º¸°ñÁö , »ý¾à¼ö¼º¿¢½º , ¼±¸ð , ¼â¾ç , õ¼Ó´Ü , ÆÄ±ØÃµ , Æ÷ºÎÀÚ , ÇØ¸¶ , È£·ÎÆÄ , Èæ³ë½Å , Achyranthes Root
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- ÀÇ»çÀÇ Ä¡·á¸¦ ¹Þ°í ÀÖ´Â »ç¶÷
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| DUR (ÀǾàǰ»ç¿ëÆò°¡) |
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°í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
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[¿¬·É´ë±Ý±â»ó¼¼°Ë»ö]
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| Mechanism of Action |
Candicidin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Ergosterol, the principal sterol in the fungal cytoplasmic membrane, is the target site of action of Candicidin. Candicidin binds irreversibly to ergosterol, resulting in disruption of membrane integrity and ultimately cell death. There is some evidence that the binding site in the cell wall may be to fatty acids or fatty acid esters and that this binding capacity must be satisfied before candicidin can bring about its lethal effect by binding to sterol in the cell membrane.
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| Pharmacology |
Candicidin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Candicidin is a polyene antifungal antibiotic produced by a strain of Streptomyces griseus. It is especially effective against Candida albicans (more effective than amphotericin B), and is administered intravaginally in the treatment of vulvovaginal candidiasis.
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| Metabolism |
Candicidin¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
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| Protein Binding |
Candicidin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
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| Half-life |
Candicidin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Not Available
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| Absorption |
Candicidin¿¡ ´ëÇÑ Absorption Á¤º¸ Not Available
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| Biotransformation |
Candicidin¿¡ ´ëÇÑ Biotransformation Á¤º¸ Not Available
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| Toxicity |
Candicidin¿¡ ´ëÇÑ Toxicity Á¤º¸ Not Available
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| Drug Interactions |
Candicidin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Altretamine Risk of severe hypotensionAtazanavir Atazanavir increases the effect and toxicity of tricyclicsCarbamazepine The tricyclic increases the effect of carbamazepineCimetidine Cimetidine increases the effect of tricyclic agentCisapride Increased risk of cardiotoxicity and arrhythmiasClonidine The tricyclic decreases the effect of clonidineDihydroquinidine barbiturate Quinidine increases the effect of tricyclic agentDobutamine The tricyclic increases the sympathomimetic effectDonepezil Possible antagonism of actionDopamine The tricyclic increases the sympathomimetic effectDuloxetine Possible increase in the levels of this agent when used with duloxetineEphedra The tricyclic increases the sympathomimetic effectEphedrine The tricyclic increases the sympathomimetic effectEpinephrine The tricyclic increases the sympathomimetic effectFenoterol The tricyclic increases the sympathomimetic effectFluoxetine Fluoxetine increases the effect and toxicity of tricyclicsFluvoxamine Fluvoxamine increases the effect and toxicity of tricyclicsGalantamine Possible antagonism of actionGrepafloxacin Increased risk of cardiotoxicity and arrhythmiasGuanethidine The tricyclic decreases the effect of guanethidineIsocarboxazid Possibility of severe adverse effectsIsoproterenol The tricyclic increases the sympathomimetic effectMephentermine The tricyclic increases the sympathomimetic effectMetaraminol The tricyclic increases the sympathomimetic effectMethoxamine The tricyclic increases the sympathomimetic effectMoclobemide Possible severe adverse reaction with this combinationNorepinephrine The tricyclic increases the sympathomimetic effectOrciprenaline The tricyclic increases the sympathomimetic effectPhenelzine Possibility of severe adverse effectsPhenylephrine The tricyclic increases the sympathomimetic effectPhenylpropanolamine The tricyclic increases the sympathomimetic effectPirbuterol The tricyclic increases the sympathomimetic effectProcaterol The tricyclic increases the sympathomimetic effectPseudoephedrine The tricyclic increases the sympathomimetic effectQuinidine Quinidine increases the effect of tricyclic agentQuinidine barbiturate Quinidine increases the effect of tricyclic agentRasagiline Possibility of severe adverse effectsRifabutin The rifamycin decreases the effect of tricyclicsRifampin The rifamycin decreases the effect of tricyclicsRitonavir Ritonavir increases the effect and toxicity of tricyclicsRivastigmine Possible antagonism of actionSalbutamol The tricyclic increases the sympathomimetic effectSibutramine Increased risk of CNS adverse effectsSparfloxacin Increased risk of cardiotoxicity and arrhythmiasTerbinafine Terbinafine increases the effect and toxicity of the tricyclicTerbutaline The tricyclic increases the sympathomimetic effectTerfenadine Increased risk of cardiotoxicity and arrhythmiasTranylcypromine Possibility of severe adverse effects
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Candicidin¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available
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| Drug Target |
[Drug Target]
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| Description |
Candicidin¿¡ ´ëÇÑ Description Á¤º¸ Candicidin is an antibiotic obtained from a streptomyces (Streptomyces griseus) and active against some fungi of the genus Candida (C. albicans). Candicidin is administered intravaginally in the treatment of vulvovaginal candidiasis.
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| Dosage Form |
Candicidin¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Not Available
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| Drug Category |
Candicidin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsAntifungal Agents
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| Smiles String Canonical |
Candicidin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(CC(C)C1OC(=O)CC(=O)CCCC(=O)CC(O)CC(O)CC(O)CC2(O)CC(O)C(C(CC(OC3OC(C)C(O)C(N)C3O)C=CC=CC=CC=CC=CC=CC=CC1C)O2)C(O)=O)C(O)CC(=O)C1=CC=C(N)C=C1
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| Smiles String Isomeric |
Candicidin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@@H](C[C@H](C)[C@H]1OC(=O)CC(=O)CCCC(=O)C[C@@H](O)C[C@@H](O)C[C@@H](O)C[C@]2(O)C[C@@H](O)[C@H]([C@@H](C[C@H](O[C@@H]3O[C@H](C)[C@@H](O)[C@H](N)[C@@H]3O)\C=C/C=C\C=C/C=C\C=C/C=C\C=C/[C@@H]1C)O2)C(O)=O)[C@@H](O)CC(=O)C1=CC=C(N)C=C1
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| InChI Identifier |
Candicidin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C59H84N2O18/c1-35-18-15-13-11-9-7-5-6-8-10-12-14-16-21-46(77-58-55(72)53(61)54(71)38(4)76-58)31-50-52(57(73)74)49(69)34-59(75,79-50)33-45(66)29-44(65)28-43(64)27-41(62)19-17-20-42(63)30-51(70)78-56(35)37(3)26-36(2)47(67)32-48(68)39-22-24-40(60)25-23-39/h5-16,18,21-25,35-38,43-47,49-50,52-56,58,64-67,69,71-72,75H,17,19-20,26-34,60-61H2,1-4H3,(H,73,74)/b6-5-,9-7-,10-8-,13-11-,14-12-,18-15-,21-16-/t35?,36?,37?,38-,43?,44?,45?,46?,47?,49?,50?,52?,53+,54-,55+,56?,58?,59?/m1/s1/f/h73H
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| Chemical IUPAC Name |
Candicidin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (19E,21E,23E,25E,27E,29E,31E)-33-[(3S,4S,5S,6R)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-17-[7-(4-aminophenyl)-5-hydroxy-4-methyl-7-oxoheptan-2-yl]-1,3,5,7,37-pentahydroxy-18-methyl-9,13,15-trioxo-16,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylic acid
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ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2024-08-26
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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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»ó¼¼Á¤º¸´Â ½ÄǰÀǾàǰ¾ÈÀüóÀÇ Á¦Ç°Çã°¡»çÇ×À» Åä´ë·Î ÀÛ¼ºµÇ¾úÀ¸¸ç ¿ä¾àÁ¤º¸´Â »ó¼¼Á¤º¸ ¹× ±âŸ¹®ÇåÀ» ±â¹ÝÀ¸·Î µå·°ÀÎÆ÷¿¡¼ ÆíÁýÇÑ ³»¿ëÀÔ´Ï´Ù. Á¦Ç°Çã°¡»çÇ×ÀÇ ¸ñÂ÷¿Í ´Ù¼Ò »óÀÌÇÒ ¼ö ÀÖ½À´Ï´Ù. |
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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
Ã¥ÀÓÀ» ÁöÁö ¾Ê½À´Ï´Ù. ÀÚ¼¼ÇÑ ³»¿ëÀº ¡°Ã¥ÀÓÀÇ ÇÑ°è ¹× ¹ýÀû°íÁö¡±¸¦ ÂüÁ¶ÇØ ÁֽʽÿÀ.
¹Ýµå½Ã Á¦Á¶¡¤¼öÀÔ»ç, ÆÇ¸Å»ç, ÀÇ»ç, ¾à»ç¿¡°Ô ÃÖÁ¾ÀûÀ¸·Î È®ÀÎÇϽñ⠹ٶø´Ï´Ù.
ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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