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    Cevimeline hydrochloride hemihydrate 153504-70-2

    簡(jiǎn)要描述:Cevimeline hydrochloride hemihydrate 153504-70-2
    Cevimeline hydrochloride hemihydrate, a novel muscarinic receptor agonist, is a candidate therapeutic drug for xerostomia in Sjogren's syndrome.

    • 產(chǎn)品型號(hào):abs47028023a
    • 廠商性質(zhì):生產(chǎn)廠家
    • 更新時(shí)間:2026-01-13
    • 訪  問  量:667

    詳細(xì)介紹

    品牌absinCAS153504-70-2
    分子式C20H38Cl2N2O3S2純度>98%
    分子量489.55貨號(hào)abs47028023
    規(guī)格10mg供貨周期現(xiàn)貨
    主要用途is a candidate therapeutic drug應(yīng)用領(lǐng)域化工,生物產(chǎn)業(yè),農(nóng)林牧漁,制藥/生物制藥,綜合

    Cevimeline hydrochloride hemihydrate 153504-70-2

    產(chǎn)品描述
    描述

    Cevimeline hydrochloride hemihydrate, a novel muscarinic receptor agonist, is a candidate therapeutic drug for xerostomia in Sjogren's syndrome.

    純度
    >98%
    儲(chǔ)存/保存方法
    Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
    基本信息
    別名
    鹽酸西維美林半水合物;SNI-2011;AF102B hydrochloride hemihydrate
    外觀
    white to tan powder
    可溶性/溶解性
    H2O : ≥ 50 mg/mL (204.27 mM)
    生物活性
    In vitro(體外研究)
    In digested parotid cells, Cevimeline (0.1-100 μM) increases the intracellular Ca2+ concentration.
    In vivo(體內(nèi)研究)
    Cevimeline (0.008-0.016 mg/kg; intraperitoneal injection; male Wistar rats) treatment shows slowly increasing and lasting salivation, and increased blood flow increment in the parotid gland and pressor response. Cevimeline inhibits angiotensin II-induced water intake and neuronal activity in the subfornical organ at 0.016 mg/kg.
    研究領(lǐng)域
    研究領(lǐng)域
    Neuroscience
    Drug DiscoverySmall Molecule DrugLead Compound Discovery
    Cevimeline hydrochloride hemihydrate 153504-70-2溫馨提示:本產(chǎn)品僅作科研實(shí)驗(yàn)使用,不支持臨床等研究

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