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Risedronic Acid

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纯度: 99.87%

货号 T0379Cas号 105462-24-6

别名 利塞膦酸, Risedronate

Risedronic Acid (Risedronate) 具有抑制破骨细胞介导的骨重吸收的作用。

Risedronic Acid
其他形式的 “Risedronic Acid”:

Risedronic Acid

一键复制产品信息
Rating icon 很棒

纯度: 99.87%

货号 T0379 别名 利塞膦酸, RisedronateCas号 105462-24-6

Risedronic Acid (Risedronate) 具有抑制破骨细胞介导的骨重吸收的作用。

规格价格库存数量
5 mg
¥ 118
现货
10 mg
¥ 158
现货
25 mg
¥ 242
现货
50 mg
¥ 343
现货
100 mg
¥ 496
现货
500 mg
¥ 1,230
现货
1 g
¥ 1,830
现货
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产品介绍


生物活性
产品描述
Risedronic Acid (Risedronate), a pyridinyl biphosphonate, can inhibit osteoclast-mediated bone resorption.
别名利塞膦酸, Risedronate
化学信息
分子量283.11
分子式C7H11NO7P2
CAS No.105462-24-6
SmilesO.OC(Cc1cccnc1)(P(O)(O)=O)P(O)(O)=O
密度1.870 g/cm3 (Predicted)
储存&溶解度
存储Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
H2O: Insoluble
DMSO: 2.84 mg/mL (10.03 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM3.5322 mL17.6610 mL35.3220 mL176.6098 mL
5 mM0.7064 mL3.5322 mL7.0644 mL35.3220 mL
10 mM0.3532 mL1.7661 mL3.5322 mL17.6610 mL

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
TargetMol | Animal experiments 比如您的给药剂量是10 mg/kg,每只动物体重20g,给药体积100 μLTargetMol | Animal experiments 一共给药动物10只,您使用的配方为5%TargetMol | reagent DMSO + 30%PEG300 + 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为2mg/mL
母液配置方法: 2 mg 药物溶于 50 μLDMSOTargetMol | reagent ( 母液浓度为 40 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween80, 混匀澄清,再加 600μLSaline/PBS/ddH2OTargetMol | reagent 混匀澄清

以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。

方案所需的各类助溶剂如: DMSOPEG300 / PEG400Tween 80SBE-β-CD玉米油 等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

TargetMol AI Summary
Risedronic Acid shows a diverse range of bioactivities, particularly in inhibiting various enzymes and parasites. It inhibits the growth of Trypanosoma brucei rhodesiense, Trypanosoma cruzi, Toxoplasma gondii, Leishmania major, and Plasmodium species, with IC50 values varying from nanomolar to micromolar levels. The compound also demonstrates significant inhibitory activity against farnesyl diphosphate synthase (FPPS) and geranylgeranyl diphosphate synthase (GGPPS) from multiple organisms, with IC50 values as low as 3.9 nM for human FPPS. Risedronic Acid shows considerable antiproliferative effects against various human and parasite cell lines. It has a notable therapeutic index, although toxicity concerns are present, particularly in its cytotoxicity against human KB and HepG2 cell lines. Additionally, it displays anti-inflammatory and bone resorption inhibition properties in rat models. Structurally, Risedronic Acid demonstrates high binding affinity to FPPS, significantly inhibiting enzyme activity and protein prenylation, indicating potential applications in treating diseases related to these pathways. Despite its broad spectrum of activity, it does not show significant inhibitory potential against Aquifex aeolicus IspH or recombinant GGTase 2 enzyme. Furthermore, it has displayed minimal antiviral activity against SARS-CoV-2 and weak binding affinity towards several human receptors..
Note: Summary generated by AI, AI may be wrong some times, we do not provide any medical advice and only sell our product to accredited institution, Please cross-check with other sources, data source: chembl
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