Vibegron (Synonyms: MK-4618)
目录号: PL14278 纯度: ≥98%
CAS No. :1190389-15-1
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中文名称
Vibegron
中文别名
维贝格隆;(S)-N-(4-(((2S,5R)-5-((R)-羟基(苯基)甲基)吡咯烷-2-基)甲基)苯基)-4-氧代-4,6,7,8-四氢吡咯并[1,2-a]嘧啶-6-甲酰胺
英文名称
Vibegron
英文别名
VIBEGRON;M5TSE03W5U;C26H28N4O3;Vibegron [USAN:INN];vibegronum;Beova;Beova (TN);MK 4618;Vibegron (JAN/USAN);GTPL10100;BDBM50146154;MK4618;compound 7 [PMID: 26709102];SB16922;Pyrrolo(1,2-a)pyrimidine-6-carboxamide, 4,6,7,8-tetrahydro-N-(4-(((2S,5R)-5-((R)-hydroxyphenylmethyl)-2-pyrrolidinyl)methyl)phenyl)-4-oxo-, (6S)-;(6S)-N-(4-(((2S,5R)-5-((R)-Hydroxyphenylmethyl)pyrrolidin-2-yl)methyl)phenyl)-4;Vibegron
Cas No.
1190389-15-1
分子式
C26H28N4O3
分子量
444.53
包装储存
4°C, sealed storage, away from moisture and light In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
产品详情
Vibegron (MK-4618) 是一种有效的,高选择性的且具有口服活性的 β3-adrenoceptor 激动剂(EC50=1.1 nM)。Vibegron 可用于膀胱过度活动相关的严重急症尿失禁。
生物活性
Vibegron (MK-4618) is a potent, highly selective and orally active β 3 -adrenoceptor agonist (EC 50 =1.1 nM). Vibegron can be used for severe urgency urinary incontinence related to overactive bladder.
性状
Solid
IC50 & Target[1][2]
β adrenergic receptor β3 adrenoceptor 1.1 nM (EC50)
体内研究(In Vivo)
Vibegron (1~12 μΜ; i.v.) exhibits dose dependent decreases in micturition pressure and increases in functional bladder capacity.
Vibegron (30 mg/kg; p.o.; 4 weeks) upregulates mRNA levels of type 1, type 3 collagen, TGF‐β1, and HIF‐1α.
Vibegron (1 and 10 mg/kg; i.v.; interval 30 minutes) (10 mg/kg) in oxo-M-treated rats makes bladder capacity significantly decreased compared with oxo-M-not treated rats (intravesical instillation of vehicle). has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moisture and light In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
ClinicalTrial
参考文献
[1]. Yoshida M, et al. Efficacy of vibegron, a novel β3-adrenoreceptor agonist, on severe urgency urinary incontinence related to overactive bladder: post hoc analysis of a randomized, placebo-controlled, double-blind, comparative phase 3 study. BJU Int. 2020;125(5):709-717.
[2]. Yoshida M, et al. Efficacy of novel β3 -adrenoreceptor agonist vibegron on nocturia in patients with overactive bladder: A post-hoc analysis of a randomized, double-blind, placebo-controlled phase 3 study. Int J Urol. 2019;26(3):369-375.
溶解度数据
In Vitro: DMSO : 95 mg/mL (213.71 mM; Need ultrasonic)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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