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Darifenacin

产品号 DB00496 公司名称 DrugBank
CAS号 133099-04-4 公司网站 http://www.ualberta.ca/
分子式 C28H30N2O2 电 话 (780) 492-3111
分子量 426.55 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 379

产品价格信息

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产品别名

标题
Darifenacin
IUPAC标准名
2-[(3S)-1-[2-(2,3-dihydro-1-benzofuran-5-yl)ethyl]pyrrolidin-3-yl]-2,2-diphenylacetamide
IUPAC传统名
enablex
商标名
Emselex
Enablex
别名
darifenacin

产品登记号

PubChem CID 444031
CAS号 133099-04-4
PubChem SID 46508104

产品性质

疏水性(logP) 4.5

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved; investigational
Description Darifenacin (Enablex?, Novartis) is a medication used to treat urinary incontinence.

Darifenacin works by blocking the M3 muscarinic acetylcholine receptor, which is primarily responsible for bladder muscle contractions. It thereby decreases the urgency to urinate. It should not be used in people with urinary retention.

It is not known whether this selectivity for the M3 receptor translates into any clinical advantage when treating symptoms of overactive bladder syndrome.
Indication For the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency and frequency.
Pharmacology Darifenacin is a competitive muscarinic receptor antagonist. In vitro studies using human recombinant muscarinic receptor subtypes show that darifenacin has greater affinity for the M3 receptor than for the other known muscarinic receptors (9 and 12-fold greater affinity for M3 compared to M1 and M5, respectively, and 59-fold greater affinity for M3 compared to both M2 and M4). Muscarinic receptors play an important role in several major cholinergically mediated functions, including contractions of the urinary bladder smooth muscle and stimulation of salivary secretion. Adverse drug effects such as dry mouth, constipation and abnormal vision may be mediated through effects on M3 receptors in these organs.
Toxicity Overdosage can potentially result in severe central anticholinergic effects.
Affected Organisms
Humans and other mammals
Biotransformation Hepatic. Primarily mediated by the cytochrome P450 enzymes CYP2D6 and CYP3A4.
Absorption The mean oral bioavailability at steady state is estimated to be 15% and 19% for 7.5 mg and 15 mg tablets, respectively.
Half Life The elimination half-life of darifenacin following chronic dosing is approximately 13-19 hours.
Protein Binding Darifenacin is approximately 98% bound to plasma proteins (primarily to alpha-1-acid-glycoprotein).
Distribution * 163 L
Clearance * 40 L/h [extensive metabolizers]
* 32 L/h [poor metabolizers]
External Links
Wikipedia
RxList
Drugs.com

参考文献