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    首頁 > 產(chǎn)品中心 > 生化試劑 > 小分子化合物 > abs47028035Revaprazan HCl 178307-42-1

    Revaprazan HCl 178307-42-1

    簡要描述:Revaprazan HCl 178307-42-1
    Revaprazan Hydrochloride is the hydrochloride salt form of a lipophilic, weak base with potassium-competitive acid blocking (P-CAB) activity.

    • 產(chǎn)品型號:abs47028035
    • 廠商性質(zhì):生產(chǎn)廠家
    • 更新時(shí)間:2026-01-14
    • 訪  問  量:734

    詳細(xì)介紹

    品牌absinCAS178307-42-1
    分子式C22H24ClFN4純度99%
    分子量398.9貨號abs47028035
    規(guī)格2mg供貨周期現(xiàn)貨
    主要用途is the hydrochloride salt form of a lipo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

    Revaprazan HCl 178307-42-1

    產(chǎn)品描述
    描述

    Revaprazan Hydrochloride is the hydrochloride salt form of a lipophilic, weak base with potassium-competitive acid blocking (P-CAB) activity. Revaprazan concentrates highly in the gastric parietal cell canaliculus and on entering this acidic environment is instantly protonated and binds competitively and reversibly to the potassium binding site of the proton pump hydrogen-potassium adenosine triphosphatase (H+/K+ ATPase), thereby inhibiting the pump's activity and the parietal cell secretion of H+ ions into the gastric lumen, the final step in gastric acid production.

    純度
    99%
    儲存/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
    可溶性/溶解性
    10 mM in DMSO
    生物活性
    靶點(diǎn)
    Proton pump
    In vitro(體外研究)
    Revaprazan Hydrochloride reversibly inhibits H+/K+-ATPase via binding to the K+-binding site of the pump. This reversibility leads to fewer adverse events. Revaprazan could inhibit H.pylori-induced COX-2 expression by blocking phosphorylation of IκB-α and Akt signaling in AGS cells. It could impose significant anti-inflammatory actions on H.pylori infection beyond acid suppression.
    In vivo(體內(nèi)研究)
    Pharmacokinetic studies of revaprazan hydrochloride in rats and dogs showed the drug had a low oral bioavailability, which was speculated to be due to first pass effect and poor water solubility of drug.
    參考文獻(xiàn)
    參考文獻(xiàn)
    • 1. Lee JS, et al.J Clin Biochem Nutr. 2012 Sep;51(2):77-83.

    • 2. Jung JW, et al. Tohoku J Exp Med. 2011;224(4):293-300.

    研究領(lǐng)域
    研究領(lǐng)域
    MetabolismTypes of disease
    Drug DiscoverySmall Molecule DrugLead Compound Discovery
    Revaprazan HCl 178307-42-1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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