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S81188

Pantoprazole

源葉(MedMol) 98%
  • 英文名:
  • Pantoprazole
  • 別名:
  • 泮托拉唑;氘代泮托拉唑-d3; 潘托拉唑;;Pantoprazol; 5-difluoromethoxy-2-(((3,4-dimethoxy-2-pyridinyl)methyl)sulfinyl)-1H-benzimidazole; Pantoprazolum; 5-(difluoromethoxy)-2-[[(3,4-dimethoxy-2-pyridyl)methyl]sulfinyl]-
  • CAS號(hào):
  • 102625-70-7
  • 分子式:
  • C16H15F2N3O4S
  • 分子量:
  • 383.37
品牌貨號(hào)產(chǎn)品規(guī)格價(jià)格(RMB) 庫(kù)存(上海) 北京 武漢 南京 數(shù)量計(jì)量單位 加入購(gòu)物車...
源葉(MedMol) S81188-100mg 98% ¥380.00元 2 0 0 0 EA 加入購(gòu)物車
源葉(MedMol) S81188-500mg 98% ¥1150.00元 預(yù)計(jì)交期:2-3天 0 0 0 EA 加入購(gòu)物車
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產(chǎn)品介紹

參考文獻(xiàn)(1篇)

質(zhì)檢證書(shū)(COA)

摩爾濃度計(jì)算器

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  • 提示:詳情請(qǐng)下載說(shuō)明書(shū)。
  • 產(chǎn)品描述: Pantoprazole (BY10232) is an orally active and potent proton pump inhibitor (PPI). Pantoprazole, a substituted benzimidazole, is a potent H+/K+-ATPase inhibitor with an IC50 of 6.8 μM. Pantoprazole improves pH stability and has anti-secretory, anti-ulcer activities. Pantoprazole significantly increased tumor growth delay combined with Doxorubicin (HY-15142)
  • 靶點(diǎn): proton pump;Apoptosis;?Protonpump;?Autophagy
  • 體內(nèi)研究:
    Pantoprazole (BY1023; 200 mg/kg; IP; once a week for 3 weeks) significantly increases tumor growth delay of MCF-7 xenografts combined with Doxorubicin. Pantoprazole (0.3-3 mg/kg, p.o.) dose-dependently decreases both basal acid secretion in pylorus-ligated rats and the stimulated acid secretion induced by mepirizole in acute fistula rats.
  • 參考文獻(xiàn):
    1. Krupa J Patel, et al. Use of the proton pump inhibitor pantoprazole to modify the distribution and activity of doxorubicin: a potential strategy to improve the therapy of solid tumors. Clin Cancer Res. 2013 Dec 15;19(24):6766-76. 2. Huarui Zhang, et al. Advances in the discovery of exosome inhibitors in cancer. J Enzyme Inhib Med Chem. 2020 Dec;35(1):1322-1330. 3. W Beil, et al. Pantoprazole: a novel H+/K(+)-ATPase inhibitor with an improved pH stability. Eur J Pharmacol. 1992 Aug 6;218(2-3):265-71. 4. K Takeuchi, et al. Effects of pantoprazole, a novel H+/K+-ATPase inhibitor, on duodenal ulcerogenic and healing responses in rats: a comparative study with omeprazole and lansoprazole. J Gastroenterol Hepatol. 1999 Mar;14(3):251-7.
  • 保存條件: 2-8℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.608 ml 13.042 ml 26.084 ml
    5 mM 0.522 ml 2.608 ml 5.217 ml
    10 mM 0.261 ml 1.304 ml 2.608 ml
    50 mM 0.052 ml 0.261 ml 0.522 ml
  • 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權(quán)威性,僅供客戶參考交流研究之用。
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