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Terazosin

产品号 DB01162 公司名称 DrugBank
CAS号 63590-64-7 公司网站 http://www.ualberta.ca/
分子式 C19H25N5O4 电 话 (780) 492-3111
分子量 387.4329 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 1033

产品价格信息

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产品别名

标题
Terazosin
IUPAC标准名
6,7-dimethoxy-2-[4-(oxolane-2-carbonyl)piperazin-1-yl]quinazolin-4-amine
IUPAC传统名
6,7-dimethoxy-2-[4-(oxolane-2-carbonyl)piperazin-1-yl]quinazolin-4-amine
商标名
Vasomet
Blavin
Fosfomic
Heitrin
Hytracin
Hytrin
Hytrinex
Itrin
Flumarc
Urodie
Vicard
别名
Terazosina [INN-Spanish]
Terazosinum [INN-Latin]
Terazosine [INN-French]
Abbott 45975
Terazosin HCl
Terazosin hydrochloride
Terazosine
Trazosin HCl

产品登记号

CAS号 63590-64-7
PubChem SID 46509129
PubChem CID 5401

产品性质

疏水性(logP) 1
溶解度 29.7mg/mL

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved
Description Terazosin is a selective alpha1-antagonist used for treatment of symptoms of benign prostatic hyperplasia (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.
Indication For the treatment of symptomatic BPH and mild to moderate hypertension.
Pharmacology Terazosin, classified as a quinazoline, is similar to doxazosin and prazosin. As an α-adrenergic blocking agent, terazosin is used to treat hypertension and BPH. Terazosin produces vasodilation and reduces peripheral resistance but in general has only a slight effect on cardiac output. The antihypertensive effect with chronic dosing is not usually accompanied by reflex tachycardia.
Toxicity LD50=259.3mg/kg (IV in mice)
Affected Organisms
Humans and other mammals
Biotransformation Hepatic. One of the four metabolites identified (piperazine derivative of terazosin) has antihypertensive activity.
Absorption Essentially completely absorbed in man (90% bioavailability).
Half Life 12 hours
Protein Binding 90-94%
Elimination Approximately 10% of an orally administered dose is excreted as parent drug in the urine and approximately 20% is excreted in the feces.
References
Cushman WC, Ford CE, Cutler JA, Margolis KL, Davis BR, Grimm RH, Black HR, Hamilton BP, Holland J, Nwachuku C, Papademetriou V, Probstfield J, Wright JT Jr, Alderman MH, Weiss RJ, Piller L, Bettencourt J, Walsh SM: Success and predictors of blood pressure control in diverse North American settings: the antihypertensive and lipid-lowering treatment to prevent heart attack trial (ALLHAT). J Clin Hypertens (Greenwich). 2002 Nov-Dec;4(6):393-404. [Pubmed]
External Links
Wikipedia
RxList
Drugs.com

参考文献

  • Cushman WC, Ford CE, Cutler JA, Margolis KL, Davis BR, Grimm RH, Black HR, Hamilton BP, Holland J, Nwachuku C, Papademetriou V, Probstfield J, Wright JT Jr, Alderman MH, Weiss RJ, Piller L, Bettencourt J, Walsh SM: Success and predictors of blood pressure control in diverse North American settings: the antihypertensive and lipid-lowering treatment to prevent heart attack trial (ALLHAT). J Clin Hypertens (Greenwich). 2002 Nov-Dec;4(6):393-404. Pubmed