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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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文献和实验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
.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
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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