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Alendronate sodium hydrate
CAS No. 121268-17-5
Alendronate sodium hydrate ( Alendronate | MK 217 | G-704650 Adronat )
产品货号. M10794 CAS No. 121268-17-5
阿仑膦酸钠水合物 (Alendronate;MK 217;G-704650 Adronat) 是一种双膦酸盐,可作为破骨细胞介导的骨吸收的特异性抑制剂。
纯度: >98% (HPLC)
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规格 | 价格/人民币 | 库存 | 数量 |
50MG | ¥324 | 有现货 |
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100MG | ¥389 | 有现货 |
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200MG | ¥437 | 有现货 |
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500MG | ¥689 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Alendronate sodium hydrate
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述阿仑膦酸钠水合物 (Alendronate;MK 217;G-704650 Adronat) 是一种双膦酸盐,可作为破骨细胞介导的骨吸收的特异性抑制剂。
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产品描述Alendronate sodium hydrate (Alendronate;MK 217;G-704650 Adronat) is a bisphosphonate that acts as a specific inhibitor of osteoclastmediated bone resorption, inhibits osteoclast protein-tyrosine phosphatase (PTPepsilon) with IC50 of 2 uM; also inhibits the activities of other bacterially expressed PTPs such as PTPsigma and CD45, suppresses in vitro formation of multinucleated osteoclasts from osteoclast precursors and in vitro bone resorption by isolated rat osteoclasts with IC50 of 10 uM; also is also inhibits farnesyl disphosphate synthase with IC50 of 1.7 uM.Osteoporosis Approved(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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体外实验——
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体内实验——
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同义词Alendronate | MK 217 | G-704650 Adronat
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通路Others
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靶点Other Targets
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受体Farnesyldiphosphatesynthase
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研究领域Metabolic Disease
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适应症Osteoporosis
化学信息
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CAS Number121268-17-5
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分子量325.1237
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分子式C4H18NNaO10P2
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纯度>98% (HPLC)
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溶解度H2O: ≥ 28.57 mg/mL; DMSO: < 3.2 mg/mL
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SMILESOC(P([O-])(O)=O)(P(O)(O)=O)CCCN.[H]O[H].[H]O[H].[H]O[H].[Na+]
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化学全称Phosphonic acid, P,P'-(4-amino-1-hydroxybutylidene)bis-, sodium salt, hydrate (1:1:3)
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Bergstrom JD, et al. Arch Biochem Biophys. 2000 Jan 1;373(1):231-41.
2. Opas EE, et al.Biochem Pharmacol. 1997 Sep 15;54(6):721-7.
3. David P, et al. J Bone Miner Res. 1996 Oct;11(10):1498-507.
4. Schmidt A, et al. Proc Natl Acad Sci U S A. 1996 Apr 2;93(7):3068-73.