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¼³ÅؽÅÁ¤ [Sulfadiazine , Tetroxoprim]
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Àü¹®ÀǾàǰ | »èÁ¦
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µå·°ÀÎÆ÷¿¡¼´Â ÀǾàǰ ÀÎÅÍ³Ý ÆÇ¸Å¸¦ ÇÏÁö ¾Ê½À´Ï´Ù. |
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À¯·áȸ¿ø °áÀç½Ã¿¡´Â º¸´Ù ´Ù¾çÇÑ ¾à¹°Á¤º¸¸¦
ÀÌ¿ëÇÏ½Ç ¼ö ÀÖ½À´Ï´Ù.
À¯·áÁ¤º¸¸ñ·ÏÀº Àü¹®È¸¿øÀ¸·Î
·Î±×ÀÎ ÇϽøé È®ÀÎ °¡´ÉÇÕ´Ï´Ù.
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| Ç׸ñ |
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û±¸ÄÚµå(KDÄÚµå) ºñ±Þ¿©Á¡°ËÄÚµå »óÇÑ±Ý¾× |
649101730[A00851201]
[º¸ÇèÄڵ忡 µû¸¥ ¾àǰ±âº»Á¤º¸ Á÷Á¢Á¶È¸]
\0 ¿ø/1Á¤(2007.03.01)(ÇöÀç¾à°¡)
\220 ¿ø/1Á¤(2005.03.01)(º¯°æÀü¾à°¡)
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´ëÀå±Õ, ½ºÆ®·Î¹ÚÅ׸£¼Ó, Ŭ·¹ºê¼¿¤¶ó¼Ó, ¿¡Å׷ιÚÅ׸£¼Ó, ÇÁ·ÎÅ׿콺¼Ó(ÇÁ·ÎÅ׿콺¹Ì¶óºô¸®½º, ÇÁ·ÎÅ׿콺 ºÒ°¡¸®½º, ÇÁ·ÎÅ׿콺 ·¹Æ®°Ô¸®, ÇÁ·ÎÅ׿콺 ¸ð¸£°¡´Ï), À屸±Õ, ÀÎÇ÷翣ÀÚ±Õ, ÀÌÁú±Õ, ÆÄ¶óµðǪ½º±Õ
[ÀûÀÀÁõ]
±Þ¸¸¼º±â°üÁö¿°, Æó¿°, ±â°üÁö Æó¿°, ±â°üÁö È®ÀåÁõ, ºÎºñµ¿¿°, ±Þ¸¸¼º?±¤¿°, Àü¸³¼±¿°, ½Å¿ì½Å¿°, ¿äµµ¿°
[Drugbank ÀÇ ¼ººÐÁ¤º¸¿¶÷] [Sulfadiazine]
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| Related FDA Approved Drug |
±âÁØ ¼ººÐ: SULFADIAZINELANTRISUL (TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE))
NEOTRIZINE (TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE))
SILDAFLO (SILVER SULFADIAZINE)
SILVADENE (SILVER SULFADIAZINE)
SSD (SILVER SULFADIAZINE)
SSD AF (SILVER SULFADIAZINE)
SULFADIAZINE (SULFADIAZINE)
SULFADIAZINE SODIUM (SULFADIAZINE SODIUM)
SULFALOID (TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE))
SULFA-TRIPLE #2 (TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE))
SULFONAMIDES DUPLEX (SULFADIAZINE; SULFAMERAZINE)
SULFOSE (TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE))
TERFONYL (TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE))
THERMAZENE (SILVER SULFADIAZINE)
TRIPLE SULFA (TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE))
TRIPLE SULFAS (TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE))
TRIPLE SULFOID (TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE))
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| DUR (ÀǾàǰ»ç¿ëÆò°¡) |
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| Mechanism of Action |
Sulfadiazine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Sulfadiazine is a competitive inhibitor of bacterial para-aminobenzoic acid (PABA), a substrate of the enzyme dihydropteroate synthetase. The inhibited reaction is necessary in these organisms for the synthesis of folic acid.
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| Pharmacology |
Sulfadiazine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Sulfadiazine is a sulfonamide antibiotic. The sulfonamides are synthetic bacteriostatic antibiotics with a wide spectrum against most gram-positive and many gram-negative organisms. However, many strains of an individual species may be resistant. Sulfonamides inhibit multiplication of bacteria by acting as competitive inhibitors of p-aminobenzoic acid in the folic acid metabolism cycle. Bacterial sensitivity is the same for the various sulfonamides, and resistance to one sulfonamide indicates resistance to all. Most sulfonamides are readily absorbed orally. However, parenteral administration is difficult, since the soluble sulfonamide salts are highly alkaline and irritating to the tissues. The sulfonamides are widely distributed throughout all tissues. High levels are achieved in pleural, peritoneal, synovial, and ocular fluids. Although these drugs are no longer used to treat meningitis, CSF levels are high in meningeal infections. Their antibacterial action is inhibited by pus.
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| Metabolism |
Sulfadiazine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
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| Protein Binding |
Sulfadiazine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
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| Half-life |
Sulfadiazine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Not Available
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| Absorption |
Sulfadiazine¿¡ ´ëÇÑ Absorption Á¤º¸ Not Available
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| Pharmacokinetics |
SulfadiazineÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : °æ±¸ : Àß Èí¼öµÈ´Ù.
- ºÐÆ÷ : ü³» Á¶Á÷°ú ´Á¸·¾×, º¹¸·¾×, Ȱ¾×, ¹æ¼ö µîÀ» Æ÷ÇÔÇÑ Ã¼¾×¿¡ ³Î¸® ºÐÆ÷
- ³úô¼ö¾×À¸·Î ½±°Ô È®»êµÈ´Ù.
- À¯ÁóºÐºñ
- ´ë»ç : N-acetylation
- ¹Ý°¨±â : 10½Ã°£
- Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : 3-6 ½Ã°£ À̳»
- ¼Ò½Ç : 15-40%°¡ ´ë»çü·Î, 43-60%°¡ ¹Ìº¯Èü·Î ½Å¹è¼³
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| Biotransformation |
Sulfadiazine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Not Available
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| Toxicity |
Sulfadiazine¿¡ ´ëÇÑ Toxicity Á¤º¸ Oral LD50 in mouse is 1500 mg/kg.
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| Drug Interactions |
Sulfadiazine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Sulfadiazine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available
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| Drug Target |
[Drug Target]
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| Description |
Sulfadiazine¿¡ ´ëÇÑ Description Á¤º¸ One of the short-acting sulfonamides used in combination with pyrimethamine to treat toxoplasmosis in patients with acquired immunodeficiency syndrome and in newborns with congenital infections. [PubChem]
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| Dosage Form |
Sulfadiazine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Not Available
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| Drug Category |
Sulfadiazine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Infective AgentsAnti-InfectivesAntiprotozoal AgentsAntiprotozoalsCoccidiostats
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| Smiles String Canonical |
Sulfadiazine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ NC1=CC=C(C=C1)S(=O)(=O)NC1=NC=CC=N1
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| Smiles String Isomeric |
Sulfadiazine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ NC1=CC=C(C=C1)S(=O)(=O)NC1=NC=CC=N1
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| InChI Identifier |
Sulfadiazine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C10H10N4O2S/c11-8-2-4-9(5-3-8)17(15,16)14-10-12-6-1-7-13-10/h1-7H,11H2,(H,12,13,14)/f/h14H
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| Chemical IUPAC Name |
Sulfadiazine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 4-amino-N-pyrimidin-2-ylbenzenesulfonamide
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