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CAS | 869113-09-7 | 纯度 | 99.72% |
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分子量 | 508.49 | 分子式 | C₂₉H₃₄BrNO₂ |
供货周期 | 现货 | 规格 | 10 mM * 1 mL |
货号 | HY-12100 | 应用领域 | 医疗卫生,化工,生物产业,制药 |
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CAS No. : 869113-09-7
MCE 国际站:Umeclidinium bromide
产品活性:Umeclidinium bromide 是一种 mAChR 拮抗剂。Umeclidinium bromide 作用于克隆的人 M1-M5 mAChRs,Ki 为 0.05 到 0.16 nM。
研究领域:GPCR/G Protein | Neuronal Signaling
作用靶点:mAChR
In Vitro: In human embryonic kidney 293 cells, Umeclidinium bromide (GSK573719A) inhibits the human ether-a-go-go-related gene channel tail current in a concentration-dependent manner (IC50=9.4 μM). Umeclidinium bromide, previously known as GSK573719, is a novel high-affinity specific mAChR antagonist. It is a potent agent that demonstrates slow functional reversibility at cloned human M3 mAChRs and at endogenous mAChR in isolated human bronchus.
In Vivo: When Umeclidinium bromide (GSK573719A) is given once daily to mice for 5 consecutive days (0.025 μg intranasally), the level of inhibition on the fifth day is modestly increased above that obtained after a single administration to the same mice (60 versus 35%, respectively). After the fifth day of dosing, the mice are rested for 5 additional days, allowing bronchomotor tone to return to baseline levels. On the sixth day, the mice receive one last dose of antagonist and are once again challenged with Mch. The level of inhibition is essentially the same as that found on the first day of testing, indicating that tolerance is not evident with repeated intranasal delivery of Umeclidinium bromide. By contrast, when Umeclidinium bromide is given orally (2.0 mg/kg) to mice at a dose 100 times the ED50 value (intranasal), there is no observable protection against an Mch challenge.
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