化学性质:
规格 | 10mM (in 1mL DMSO) 10mg 100mg 1g |
CAS | 13 |
别名 |
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化学名 | 2-[(3S)-1-[2-(2,3-dihydro-1-benzofuran-5-yl)ethyl]pyrrolidin-3-yl]-2,2-diphenylacetamide;hydrobromide |
分子式 | C28H31BrN2O2 |
分子量 | 507.48 |
溶解度 | ≥ 20.2mg/mL in DMSO |
储存条件 | Store at -20°C |
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. |
Shipping Condition | Evaluation sample solution : ship with blue ice |
产品描述:
DarifenacinHBr(UK88525) is a selective M3 muscarinic receptor antagonist with pKi of 8.9 [1].
Themuscarinic acetylcholine receptor, also known as cholinergic/acetylcholine receptor M3, or themuscarinic 3, is amuscarinic acetylcholine receptorencoded by the human geneCHRM3. The M3muscarinic receptors are widely expressed in tissues such as smooth muscles, theendocrineglands, the exocrine glands, lungs and pancreas.M3 muscarinic receptor is involved in smooth muscle contraction and increases glandular secretions [2].
In vitro: In a model of the blood-brain barrier (BBB) and blood-ocular barrier (BOB), Darifenacin was a substrate for the P-gp drug efflux transporter. Darifenacin increased ATPase activity in a concentration-dependent manner in P-gp membranes with an ED50 value of 1.6 μM.Darifenacin treatment (100 nM) showed a significantly greater permeability for darifenacin in the basolateral to apical direction resulting in an efflux ratio in BBMEC monolayers of approximately 2.6 [3].
In vivo: Darifenacin dose-dependently inhibited the amplitude of volume-induced bladder contractions(VIBCAMP), producing 35% inhibition at dose of 283.3 nmol/kg and maximal inhibition of approximately 50–55%[1].In female Sprague-Dawley rats, administration of darifenacin (0.1 mg/kg i.v.) reduced bladder afferent activity in Aδ and C fibers. The decrease of afferent spikes in C fibers was more pronounced than that in Aδ fibers [3]. In patients with overactive bladder (OAB), darifenacin at a dose of 7.5 mg and 15 mg exihibited a rapid onset of effect, with significant improvement compared with placebo being seen for most parameters at the first clinic visit (week 2). Darifenacin administration (7.5 mg and 15 mg, daily) reduced the number of incontinence episodes per week from baseline by 67.7% and 72.8% respectively compared with 55.9% with placebo in patients with overactive bladder (OAB). Darifenacin (7.5 mg and 15 mg, daily) also showed significantly superior to placebo for improvements in micturition frequency, bladder capacity, frequency of urgency, number of incontinence episodes and severity of urgency leading to a change in clothing or pads in patients with overactive bladder (OAB) [4].
特别提醒:
1. 本产品仅供科研使用。请勿用于医药、临床诊断或治疗,食品及化妆品等用途。请勿存放于普通住宅区。
2. 为了您的安全和健康,请穿好实验服并佩戴一次性手套和口罩操作。
标签:Darifenacin HBr
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