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Alendronate sodium hydrate

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  • 2025年07月14日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      4°C, sealed storage, away from moisture

    • 英文名

      Alendronate; MK 217; G-704650 Adronat

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • CAS号

      121268-17-5

    • 规格

      10 mM * 1 mL/100 mg/500 mg

    规格:10 mM * 1 mL产品价格:¥550.0
    规格:100 mg产品价格:¥500.0
    规格:500 mg产品价格:¥1600.0

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    Alendronate sodium hydrate

    CAS No. : 121268-17-5

    MCE 国际站:Alendronate sodium hydrate

    产品活性:Alendronate sodium hydrate 是一种 farnesyl diphosphate synthase 抑制剂,IC50 值为 460 nM。

    研究领域:Others

    作用靶点:Others

    In Vitro: Alendronate, acting directly on osteoclasts, inhibits a rate-limiting step in the cholesterol biosynthesis pathway, essential for osteoclast function. Alendronate inhibits the isoprenoid biosynthesis pathway and interferes with protein prenylation, as a result of reduced geranylgeranyl diphosphate levels. Alendronate inhibits the incorporation of [3H]mevalonolactone into proteins of 18-25 kDa and into nonsaponifiable lipids, including sterols in osteoclasts. Alendronate causes a dose-dependent inhibition of [3H]MVA incorporation into sterols and a concomitant increase in incorporation of radiolabel into IPP and DMAPP.

    In Vivo: Alendronate causes erosions in the rabbit stomach, but not antral ulceration in rats. Alendronate increases the incidence and size of indomethacin-induced antral ulcers. Alendronate also enhances indomethacin-induced gastricdamage in the rat, and delays gastric ulcer healing. Alendronate (0.04-0.1 mg/kg twice weekly or 0.1 mg/kg weekly) partially blocks the establishment of bone metastases by human PC-3 ML cells and results in tumor formation in the peritoneum and other soft tissues. Alendronate pretreatment of mice (0.1 mg/kg twice weekly or weekly) and dosing along with taxol (10-50 mg/kg/day, twice weekly, or weekly) blocks the growth of PC-3 ML tumors in the bone marrow and soft tissues in a statistically significant manner and improves survival rates significantly by 4-5 weeks.

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    图标文献和实验
    相关实验
    • Protocol for Silver Staining

      0,02% sodium thiosulfate for 1 min.5)Rinse with water for 1 min.2X.0.02% Sodium Thiosulfate: For 1 gel,add 30mg sodium thiosulfate-5 hydrate to 150ml water.Silver reaction6)Submerge gel in 150ml 0.1% silver nitrate with 0.08% formalin (37%)for 20 min

    • 酶法、热修复、微波法修复抗原

      .0 ml Ultra-pure water 978.0 ml 0.5% sodium hydroxide solution 0.5% hydrochloric acid solution Xylene Industrial methylated spirits (IMS) or methanol Method Dewax and re-hydrate the paraffin sections by placing them in 3 changes

    • 其他镇静催眠药

      佚名         水合氯醛(chloral hydrate)口服易吸收,用於催眠,约15分钟起效,维持6~8小时。此药不缩短快动眼睡眠的时间,停药时也无代偿性快动眼睡眠时间延长。对胃有刺激性,须稀释后口服。久服也可引起耐受性、依赖性和成瘾性。     甲丙氨酯(meprobamate,眠尔通)、格鲁米特(glutethimide)和甲喹酮

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