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| Mechanism of Action |
Terazosin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Terazosin selectively and competitively inhibits vascular postsynaptic alpha(1)-adrenergic receptors, resulting in peripheral vasodilation and a reduction of vascular resistance and blood pressure. Unlike the nonselective alph-adrenergic blockers phenoxybenzamine and phentolamine, terazosin does not block presynaptic alpha(2)-receptors and, hence, does not cause reflex activation of norepinephrine release to produce reflex tachycardia.
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| Pharmacology |
Terazosin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Terazosin, classified as a quinazoline, is similar to doxazosin and prazosin. As an alpha-adrenergic blocking agent, terazosin is used to treat hypertension and benign prostatic hypertrophy (BPH). Terazosin produces vasodilation and reduces peripheral resistance but in general has slight effect on cardiac output. Antihypertensive effect with chronic dosing is usually not accompanied by reflex tachycardia.
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| Protein Binding |
Terazosin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 90-94%
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| Half-life |
Terazosin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 12 hours
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| Absorption |
Terazosin¿¡ ´ëÇÑ Absorption Á¤º¸ Essentially completely absorbed in man (90% bioavailability).
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| Pharmacokinetics |
Terazosin HClÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : °æ±¸ : ºü¸£°Ô Èí¼öµÈ´Ù.
- ´Ü¹é°áÇÕ : 90-95%
- ´ë»ç : ÁÖ·Î °£¿¡¼ ´ë»çµÈ´Ù.
- ¹Ý°¨±â : 9.2-12½Ã°£
- ÃÖ´ëÈ¿°ú ¹ßÇö½Ã°£ : 1½Ã°£ À̳»
- ¼Ò½Ç : ÁÖ·Î º¯°ú (60%) ´¢·Î (40%) ¹è¼³µÈ´Ù.
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| Biotransformation |
Terazosin¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic. One of the four metabolites identified (piperazine derivative of terazosin) has antihypertensive activity.
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| Toxicity |
Terazosin¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50=259.3mg/kg (i.v. in mice)
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| Drug Interactions |
Terazosin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Drug Target |
[Drug Target]
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| Description |
Terazosin¿¡ ´ëÇÑ Description Á¤º¸ Terazosin is a selective alpha 1 antagonist used for treatment of symptoms of prostate enlargement (BPH). It also acts to lower blood pressure, so it is a drug of choice for men with hypertension and prostate enlargement. It works by blocking the action of adrenaline on smooth muscle of the bladder and the blood vessel walls.
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| Drug Category |
Terazosin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Adrenergic alpha-AntagonistsAntineoplastic AgentsPlatelet Aggregation Inhibitors
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| Smiles String Canonical |
Terazosin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ COC1=C(OC)C=C2C(N)=NC(=NC2=C1)N1CCN(CC1)C(=O)C1CCCO1
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| Smiles String Isomeric |
Terazosin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ COC1=C(OC)C=C2C(N)=NC(=NC2=C1)N1CCN(CC1)C(=O)[C@H]1CCCO1
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| InChI Identifier |
Terazosin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C19H25N5O4/c1-26-15-10-12-13(11-16(15)27-2)21-19(22-17(12)20)24-7-5-23(6-8-24)18(25)14-4-3-9-28-14/h10-11,14H,3-9H2,1-2H3,(H2,20,21,22)/f/h20H2
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| Chemical IUPAC Name |
Terazosin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ [4-(4-amino-6,7-dimethoxyquinazolin-2-yl)piperazin-1-yl]-(oxolan-2-yl)methanone
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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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