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8) ½ÅÀå : ¶§¶§·Î ºÎÁ¾, ½Å°á¼®, ¿° ¹× ü¾×Àú·ù°¡ ³ªÅ¸³¯ ¼ö ÀÖ´Ù(´Ü, ü¾×Àú·ù ¹× ºÎÁ¾Àº ÇÊ¿ä½Ã ÀÌ´¢Á¦·Î Ä¡·áÇÒ ¼ö ÀÖ´Ù).
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FDA : Cµî±Þ
(minoxidil topical )
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Pharmacokinetics
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Mechanism of Action
Minoxidil¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Minoxidil is thought to promote the survival of human dermal papillary cells (DPCs) or hair cells by activating both extracellular signal-regulated kinase (ERK) and Akt and by preventing cell death by increasing the ratio of BCl- 2/Bax. Minoxidil may stimulate the growth of human hairs by prolonging anagen through these proliferative and anti-apoptotic effects on DPCs. Minoxidil, when used as a vasodilator, acts by opening adenosine triphosphate-sensitive potassium channels in vascular smooth muscle cells. This vasodilation may also improve the viability of hair cells or hair follicles.
Pharmacology
Minoxidil¿¡ ´ëÇÑ Pharmacology Á¤º¸ Minoxidil is an orally effective direct acting peripheral vasodilator that reduces elevated systolic and diastolic blood pressure by decreasing peripheral vascular resistance. Minoxidil is also used topically to treat androgenetic alopecia. Microcirculatory blood flow in animals is enhanced or maintained in all systemic vascular beds. In man, forearm and renal vascular resistance decline; forearm blood flow increases while renal blood flow and glomerular filtration rate are preserved. The predominant site of minoxidil action is arterial. Venodilation does not occur with minoxidil; thus, postural hypotension is unusual with its administration. The antihypertensive activity of minoxidil is due to its sulphate metabolite, minoxidil sulfate.
Absorption
Minoxidil¿¡ ´ëÇÑ Absorption Á¤º¸ Minoxidil is at least 90% absorbed from the GI tract in experimental animals and man.
Pharmacokinetics
MinoxidilÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
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´ë»ç : 88%°¡ ÀÏÂ÷ÀûÀ¸·Î glucuronidationÀ¸·Î ´ë»ç
»ýü³»ÀÌ¿ë·ü : °æ±¸ : 90%
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¼Ò½Ç : 12%°¡ ¹Ìº¯Èü·Î ½Å ¹è¼³µÊ
Toxicity
Minoxidil¿¡ ´ëÇÑ Toxicity Á¤º¸ Oral LD50 in rats has ranged from 1321-3492 mg/kg; in mice, 2456-2648 mg/kg. Side effects include cardiovascular effects associated with hypotension such as sudden weight gain, rapid heart beat, faintness or dizziness.
Drug Interactions
Minoxidil¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Drug Target
[Drug Target]
Description
Minoxidil¿¡ ´ëÇÑ Description Á¤º¸ A potent direct-acting peripheral vasodilator (vasodilator agents) that reduces peripheral resistance and produces a fall in blood pressure. (From Martindale, The Extra Pharmacopoeia, 30th ed, p371)
Dosage Form
Minoxidil¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Liquid TopicalSolution TopicalTablet Oral
Drug Category
Minoxidil¿¡ ´ëÇÑ Drug_Category Á¤º¸ Antihypertensive AgentsVasodilator Agents
Smiles String Canonical
Minoxidil¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ [H]N=C1N=C(C=C(N)N1O)N1CCCCC1
Smiles String Isomeric
Minoxidil¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ [H]\N=C1/N=C(C=C(N)N1O)N1CCCCC1
InChI Identifier
Minoxidil¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C9H15N5O/c10-7-6-8(12-9(11)14(7)15)13-4-2-1-3-5-13/h6,11,15H,1-5,10H2/b11-9+
Chemical IUPAC Name
Minoxidil¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 3-hydroxy-2-imino-6-piperidin-1-ylpyrimidin-4-amine
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