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¡á ½ÉÀÇ¹è°æ
Nicergoline10mg °æ±¸Á¦(ǰ¸í: »ç¹Ì¿ÂÁ¤ µî)ÀÇ ¿ä¾ç±Þ¿©±âÁØÀÇ ÀÎÁ¤´ë»ó Áß ³úÃâÇ÷ÈÄÀ¯Áõ ¹üÁÖ¿¡ ¿Ü»ó¼º ³úÃâÇ÷ Á¦¿Ü ¿©ºÎ¸¦ ¸íÈ®È÷ ÇØ ÁÙ °ÍÀ» ¿äûÇÏ¿© ºÎÀÇÇÔ.
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¡Û Nicergoline 5mg, 10mg °æ±¸Á¦(ǰ¸í: »ç¹Ì¿ÂÁ¤ µî) ÀÎÁ¤±âÁØ (°í½Ã Á¦2008-69È£, 2008.7.1)
¡Û ½Ä¾àû Çã°¡»çÇ×
¡Û Goodman & Gilman's The Pharmacological Basis Of Therapeutics, 10th edition, p248
¡Û Martindale, 35th edition, p2133
¡Û Li X-F, et al. Effect of nicergoline on cognition function of patients with cerebral infarction. Zhongguo Linchuang Kangfu, 2005 Volume 9 Issue 9 Pages 186-7
¡Û Elwan O, et al. Ergoloids and ischaemic strokes; efficacy and mechanism of action. J Int Med Res. 1995 May-Jun;23(3):154-66.
¡Û OTOMO Eiichi, et al. Clinical Evaluation of TA-079 (Nicergoline) in the Treatment of Cerebrovascular Disorders: Dose Finding Study in Well Controlled Trial, Rinsho Iyaku (Journal of Clinical Therapeutics and Medicines), 1986 Volume 2 Issue 3 Pages 417-466.
¡Û Pi©©kowska E, et al. [Nicergoline in the treatment of patients after a mild ischemic stroke] Neurol Neurochir Pol. 2002 Nov-Dec;36(6):1075-85.
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5. 1Â÷¼º ÅðÇ༺ġ¸Å, Ç÷°ü¼º Ä¡¸Å ¹× º¹ÇÕ¼ºÄ¡¸Å¿Í °ü·ÃµÈ ´ÙÀ½ Ä¡¸ÅÁõÈıºÀÇ ÀÏÂ÷Àû Ä¡·á: ±â¾ï·Â ¼Õ»ó, ÁýÁß·ÂÀå¾Ö,ÆÇ´Ü·ÂÀå¾Ö, Àû±Ø¼ººÎÁ·, Á¤¼ÀûÀå¾Ö ¢Ñ [»ç¹Ì¿ÂÁ¤-30mg]
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Çã°¡»çÇ× 1ÀÇ ÀûÀÀÁõ ¿ë¾îº¯°æ
¡Û Folia Pharmacol, Japan, 87, 537~549, 1986
¡ÛNicergolin¡¸use and administration ¡¹Martindale, 693~8, 1983,
¡Û Proof of therapeutical effectiveness of nootropic and vasoactivedrug, :173~184, 1985
¡Û Calvagno M. Usefulness of an ¥á-adrenergic blocking agent(nicergoline) in the treatment of diabetic angiopathy of lower limbs. Farmaco[Prat]Jun;37(6):200-5, 1982
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´ç´¢º´¼º¸»ÃʼøÈ¯Àå¾Ö °³¼± ¸ñÀûÀ¸·Î Åõ¿©µÈ NicergolineÁ¦Á¦(ǰ¸í : »ç¹Ì¿Â 5mg, 10mg)´Â ½ÄǰÀǾàǰ¾ÈÀüûÀå Çã°¡ ÀÚ·á¿Í ±³°ú¼¹× Âü°í¹®Çå¿¡¼ µ¿ ¾àÁ¦ Åõ¿©ÀÇ ÀÓ»óÀû È¿°ú¿¡ ´ëÇÑ È®ÀÎÀÌ °ï¶õÇϹǷΠ½ÄǰÀǾàǰ¾ÈÀüûÀå Çã°¡»çÇ×ÀÎ ¡°»çÁöÀÇ Æó»ö¼ºµ¿¸ÆÁúȯ¡±, ¡°·¹À̳뺴¹× ·¹À̳ëÁõÈıº¡± µîÀÇ ¸»ÃʼøÈ¯Àå¾Ö¿¡ ÀÎÁ¤ÇÏ°í ¡°´ç´¢º´¼º ¸»ÃʼøÈ¯Àå¾Ö¡±¿¡ Åõ¿©½Ã´Â ÀÎÁ¤ÇÏÁö ¾Æ´ÏÇÔ.(¿ä¾ç±â°üÀÇ»çÀüÀÎÁö¸¦ À§ÇØ 2008.6.1 Á¢¼öºÐ ºÎÅÍ Àû¿ë)
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Mechanism of Action
Nicergoline¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Nicergoline acts by inhibiting the postsynaptic alpha(1)-adrenoceptors on vascular smooth muscle. This inhibits the vasoconstrictor effect of circulating and locally released catecholamines (epinephrine and norepinephrine), resulting in peripheral vasodilation. Therefore the mechanism of Nicergoline is to increase vascular circulation in the brain, thereby enhancing the transmission of nerve signals across the nerve fibres, which secrete acetylcholine as a neural transmitter.
Pharmacology
Nicergoline¿¡ ´ëÇÑ Pharmacology Á¤º¸ Nicergoline is a potent vasodilator (improves brain blood flow). On the cerebral level it prompts a lowering of vascular resistance, an increase in arterial flow and stimulates the use of oxygen and glucose. Nicergoline also improves blood circulation in the lungs and limbs and has been shown to inhibit blood platelet aggregation.
Metabolism
Nicergoline¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 2D6 (CYP2D6)
Protein Binding
Nicergoline¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
Half-life
Nicergoline¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Not Available
Pharmacokinetics
NicergolineÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : °æ±¸ : 1-1.5 ½Ã°£
Èí¼ö
½Å¼ÓÇÏ°Ô Èí¼öµÊ
Èí¼öÀ² : 90-100%
´Ü¹é°áÇÕ
albumin : 82-87%
¥á1-acid glycoprotein : 43%
´ë»ç : ´ëºÎºÐ(90%) ´ë»çµÊ. ÁÖ·Î °¡¼öºÐÇØ, Å»¸ÞÆ¿È ¹ÝÀÀÀ» °Åħ.
¹Ý°¨±â : 2.5 ½Ã°£
¼Ò½Ç : 70-80%°¡ ¹Ìº¯Èü ¹× ´ë»çü·Î¼ ½Å¹è¼³µÊ.
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Food Interaction
Nicergoline¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available
Drug Target
[Drug Target]
Description
Nicergoline¿¡ ´ëÇÑ Description Á¤º¸ An ergot derivative that has been used as a cerebral vasodilator and in peripheral vascular disease. It has been suggested to ameliorate cognitive deficits in cerebrovascular disease. [PubChem]
Drug Category
Nicergoline¿¡ ´ëÇÑ Drug_Category Á¤º¸ Adrenergic alpha-AntagonistsNootropic AgentsVasodilator Agents
Smiles String Canonical
Nicergoline¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ COC12CC(COC(=O)C3=CC(Br)=CN=C3)CN(C)C1CC1=CN(C)C3=CC=CC2=C13
Smiles String Isomeric
Nicergoline¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CO[C@]12C[C@@H](COC(=O)C3=CC(Br)=CN=C3)CN(C)[C@@H]1CC1=CN(C)C3=CC=CC2=C13
InChI Identifier
Nicergoline¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C24H26BrN3O3/c1-27-13-17-8-21-24(30-3,19-5-4-6-20(27)22(17)19)9-15(12-28(21)2)14-31-23(29)16-7-18(25)11-26-10-16/h4-7,10-11,13,15,21H,8-9,12,14H2,1-3H3/t15-,21-,24+/m1/s1
Chemical IUPAC Name
Nicergoline¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ Not Available
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