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1000TABS |
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279600ATB
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°í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
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Glutamine¿¡ ´ëÇÑ µ¶¼ºÁ¤º¸ : Á¤º¸º¸±â
Ãâó: ±¹¸³µ¶¼º°úÇпø µ¶¼º¹°ÁúÁ¤º¸DB : http://www.nitr.go.kr/nitr/contents/m134200/view.do |
| Mechanism of Action |
L-Glutamine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Supplemental L-glutamine's possible immunomodulatory role may be accounted for in a number of ways. L-glutamine appears to play a major role in protecting the integrity of the gastrointestinal tract and, in particular, the large intestine. During catabolic states, the integrity of the intestinal mucosa may be compromised with consequent increased intestinal permeability and translocation of Gram-negative bacteria from the large intestine into the body. The demand for L-glutamine by the intestine, as well as by cells such as lymphocytes, appears to be much greater than that supplied by skeletal muscle, the major storage tissue for L-glutamine. L-glutamine is the preferred respiratory fuel for enterocytes, colonocytes and lymphocytes. Therefore, supplying supplemental L-glutamine under these conditions may do a number of things. For one, it may reverse the catabolic state by sparing skeletal muscle L-glutamine. It also may inhibit translocation of Gram-negative bacteria from the large intestine. L-glutamine helps maintain secretory IgA, which functions primarily by preventing the attachment of bacteria to mucosal cells. L-glutamine appears to be required to support the proliferation of mitogen-stimulated lymphocytes, as well as the production of interleukin-2 (IL-2) and interferon-gamma (IFN-gamma). It is also required for the maintenance of lymphokine-activated killer cells (LAK). L-glutamine can enhance phagocytosis by neutrophils and monocytes. It can lead to an increased synthesis of glutathione in the intestine, which may also play a role in maintaining the integrity of the intestinal mucosa by ameliorating oxidative stress. The exact mechanism of the possible immunomodulatory action of supplemental L-glutamine, however, remains unclear. It is conceivable that the major effect of L-glutamine occurs at the level of the intestine. Perhaps enteral L-glutamine acts directly on intestine-associated lymphoid tissue and stimulates overall immune function by that mechanism, without passing beyond the splanchnic bed.
Sucralfate¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Although sucralfate's mechanism is not entirely understood, there are several factors that most likely contribute to its action. Sucralfate, with its strong negative charge, binds to exposed positively-charged proteins at the base of ulcers. In this way, it coats the ulcer and forms a physical barrier that protects the ulcer surface from further injury by acid and pepsin. It directly inhibits pepsin (an enzyme that breaks apart proteins) in the presence of stomach acid and binds bile salts coming from the liver via the bile thus protecting the stomach lining from injury caused by the bile acids. Sucralfate may increase prostaglandin production, and prostaglandins are known to protect the lining of the stomach and may also bind epithelial growth factor and fibroblast growth factor, both of which enhance the growth and repair mechanism of the stomach lining.
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| Pharmacology |
L-Glutamine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Like other amino acids, glutamine is biochemically important as a constituent of proteins. Glutamine is also crucial in nitrogen metabolism. Ammonia (formed by nitrogen fixation) is assimilated into organic compounds by converting glutamic acid to glutamine. The enzyme which accomplishes this is called glutamine synthetase. Glutamine can then be used as a nitrogen donor in the biosynthesis of many compounds, including other amino acids, purines, and pyrimidines.
Sucralfate¿¡ ´ëÇÑ Pharmacology Á¤º¸ Sucralfate is a prescription medication used to treat peptic ulcers. The current clinical uses of sucralfate are limited. It is effective for the healing of duodenal ulcers, but it is not frequently used for this since more effective drugs (e.g. proton pump inhibitors) have been developed. Although the mechanism of sucralfate's ability to accelerate healing of duodenal ulcers remains to be fully defined, it is known that it exerts its effect through a local, rather than systemic, action. Chemically, sucralfate is a complex of the disaccharide sugar, sucrose, combined with sulfate and aluminum. In acidic solutions (e.g. gastric acid) it forms a thick paste that has a strong negative charge.
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| Metabolism |
L-Glutamine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Glutamine Synthetase
Sucralfate¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
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| Protein Binding |
Sucralfate¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
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| Half-life |
Sucralfate¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Not known.
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| Absorption |
L-Glutamine¿¡ ´ëÇÑ Absorption Á¤º¸ Absorption is efficient and occurs by an active transport mechanism
Sucralfate¿¡ ´ëÇÑ Absorption Á¤º¸ Minimally absorbed from the gastrointestinal tract (up to 5% of the disaccharide component and less than 0.02% of aluminum).
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| Pharmacokinetics |
SucralfateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ÀÛ¿ë¹ßÇö½Ã°£ : °æ±¸ : À§±Ë¾çÁúȯ : ±Ë¾çºÎÀ§¸¦ µµÆ÷ÇÏ´Â µ¥ °É¸®´Â ½Ã°£ : 1-2 ½Ã°£
- ÀÛ¿ëÁö¼Ó½Ã°£ : °æ±¸ : À§±Ë¾çÁúȯ : 6½Ã°£
- Èí¼ö : À§Àå°üÀ» ÅëÇØ °ÅÀÇ Èí¼öµÇÁö ¾ÊÀ½
- »ýü³»ÀÌ¿ë·ü : °æ±¸Åõ¿©½Ã : 5 %¹Ì¸¸
- ºÐÆ÷ : ±Ë¾çºÎÀ§ ±¹¼ÒÀûÀ¸·Î µµÆ÷
- ´ë»ç : ´ë»çµÇÁö ¾ÊÀ½
- ¼Ò½Ç : ´¢¹è¼³ : 0.5-2.2 %
L-GlutamineÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
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Sodium BicarbonateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- È¿°ú ¹ßÇö ½Ã±â :
- °æ±¸ : 15ºÐ
- Á¤¸ÆÁÖ»ç : ½Å¼ÓÈ÷ ¹ßÇö
- ÀÛ¿ëÁö¼Ó ½Ã°£ :
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- Á¤¸ÆÁÖ»ç : 8-10 ºÐ
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- ¼Ò½Ç : ½ÅÀå¿¡¼ ÀçÈí¼öµÇ¸ç, 1% ¹Ì¸¸ÀÌ ´¢¹è¼³µÊ
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| Biotransformation |
L-Glutamine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Enterocytes, Hepatic
Sucralfate¿¡ ´ëÇÑ Biotransformation Á¤º¸ Not Available
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| Toxicity |
L-Glutamine¿¡ ´ëÇÑ Toxicity Á¤º¸ Doses of L-glutamine up to 21 grams daily appear to be well tolerated. Reported adverse reactions are mainly gastrointestinal and not common. They include constipation and bloating. There is one older report of two hypomanic patients whose manic symptoms were exacerbated following the use of 2 to 4 grams daily of L-glutamine. The symptoms resolved when the L-glutamine was stopped. These patients were not rechallenged, nor are there any other reports of this nature.
Sucralfate¿¡ ´ëÇÑ Toxicity Á¤º¸ Acute oral toxicity (LD50) in mice is >8000 mg/kg. There is limited experience in humans with overdosage of sucralfate. Sucralfate is only minimally absorbed from the gastrointestinal tract and thus risks associated with acute overdosage should be minimal. In rare reports describing sucralfate overdose, most patients remained asymptomatic.
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| Drug Interactions |
L-Glutamine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
Sucralfate¿¡ ´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 |
Sucralfate¿¡ ´ëÇÑ Food Interaction Á¤º¸ Avoid alcohol.Take on empty stomach: 1 hour before or 2 hours after meals.Take with a full glass of water.Do not take calcium, aluminum, magnesium or Iron supplements within 2 hours of taking this medication.
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| Drug Target |
[Drug Target]
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| Description |
L-Glutamine¿¡ ´ëÇÑ Description Á¤º¸ A non-essential amino acid present abundantly throughout the body and is involved in many metabolic processes. It is synthesized from glutamic acid and ammonia. It is the principal carrier of nitrogen in the body and is an important energy source for many cells. [PubChem]
Sucralfate¿¡ ´ëÇÑ Description Á¤º¸ A basic aluminum complex of sulfated sucrose. [PubChem]
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| Dosage Form |
L-Glutamine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Not Available
Sucralfate¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Suspension OralTablet Oral
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| Drug Category |
Sucralfate¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Ulcer Agents
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| Smiles String Canonical |
L-Glutamine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ NC(CCC(N)=O)C(O)=O
Sucralfate¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.[Al].[Al].[Al].[Al].[Al].[Al].[Al].[Al].[Al].OS(=O)(=O)OCC1OC(OC2(COS(O)(=O)=O)OC(OS(O)(=O)=O)C(OS(O)(=O)=O)C2OS(O)(=O)=O)C(OS(O)(=O)=O)C(OS(O)(=O)=O)C1OS(O)(=O)=O
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| Smiles String Isomeric |
L-Glutamine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ N[C@@H](CCC(N)=O)C(O)=O
Sucralfate¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.[Al].[Al].[Al].[Al].[Al].[Al].[Al].[Al].[Al].OS(=O)(=O)OC[C@H]1O[C@@H](O[C@]2(COS(O)(=O)=O)O[C@H](OS(O)(=O)=O)[C@@H](OS(O)(=O)=O)[C@@H]2OS(O)(=O)=O)[C@H](OS(O)(=O)=O)[C@@H](OS(O)(=O)=O)[C@@H]1OS(O)(=O)=O
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| InChI Identifier |
L-Glutamine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C5H10N2O3/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H2,7,8)(H,9,10)/t3-/m0/s1/f/h9H,7H2
Sucralfate¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C11H20O35S8.9Al.20H2O/c12-47(13,14)36-1-3-4(41-49(18,19)20)5(42-50(21,22)23)6(43-51(24,25)26)9(38-3)39-11(2-37-48(15,16)17)8(45-53(30,31)32)7(44-52(27,28)29)10(40-11)46-54(33,34)35;;;;;;;;;;;;;;;;;;;;;;;;;;;;;/h3-10H,1-2H2,(H,12,13,14)(H,15,16,17)(H,18,19,20)(H,21,22,23)(H,24,25,26)(H,27,28,29)(H,30,31,32)(H,33,34,35);;;;;;;;;;20*1H2/t3-,4-,5+,6-,7+,8+,9+,10-,11-;;;;;;;;;;;;;;;;;;;;;;;;;;;;;/m1............................./s1/f/h12,15,18,21,24,27,30,33H;;;;;;;;;;;;;;;;;;;;;;;;;;;;;
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| Chemical IUPAC Name |
L-Glutamine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (2S)-2,5-diamino-5-oxopentanoic acid
Sucralfate¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ aluminum; [(2R,3S,4S,5R)-4,5-disulfooxy-2-(sulfooxymethyl)-2-[(2S,3R,4S,5R,6R)-3,4,5-trisulfooxy-6-(sulfooxymethyl)oxan-2-yl]oxyoxolan-3-yl] hydrogen sulfate; icosahydrate
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| Drug-Induced Toxicity Related Proteins |
GLUTAMINE ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:Latent transforming growth factor beta-binding protein, isoform 1L Drug:glutamine Toxicity:apoptosis. [¹Ù·Î°¡±â] Replated Protein:Glucosamine--fructose-6-phosphate aminotransferase Drug:glutamine Toxicity:arrest cellular proliferation . [¹Ù·Î°¡±â] Replated Protein:Epidermal growth factor receptor Drug:glutamine Toxicity:arrest cellular proliferation . [¹Ù·Î°¡±â] Replated Protein:Glucosamine--fructose-6-phosphate aminotransferase Drug:glutamine Toxicity:apoptosis. [¹Ù·Î°¡±â]
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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