IC2940 沙苑子苷 A 抑制剂/拮抗剂/激动剂 索莱宝

IC2940 沙苑子苷 A 抑制剂/拮抗剂/激动剂 索莱宝

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  • ¥900 - 2000
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  • 北京
  • IC2940
  • 2025年07月23日
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    • 详细信息
    • 技术资料
    • 保存条件

      Powder:-20℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year

    • 保质期

      Powder:-20℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year

    • 英文名

      Complanatoside A

    • 库存

      现询

    • 供应商

      北京索莱宝科技有限公司

    • CAS号

      146501-37-3

    • 规格

      20mg/10mg/5mg

    规格:20mg产品价格:¥2000.0
    规格:10mg产品价格:¥1320.0
    规格:5mg产品价格:¥900.0

    基本信息
    CASNo.146501-37-3
    中文名称沙苑子苷 A
    英文名称Complanatoside A
    分子式C27H30O18
    分子量642.52
    溶解性Soluble in DMSO ≥1mg/mL
    纯度≥98%
    外观(性状)Solid
    储存条件Powder:-20℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
    SMILESO=C1C(O[C@@H]([C@@H]([C@@H](O)[C@@H]2O)O)O[C@@H]2CO)=C(C3=CC(O)=C(O[C@@H]([C@@H]([C@@H](O)[C@@H]4O)O)O[C@@H]4CO)C(O)=C3)OC5=CC(O)=CC(O)=C15
    靶点Others
    通路Others
    背景说明是一种存在于沙苑子中的一种黄酮苷,具有生物或化学活性。
    In VitroA simple and sensitive LC-MS/MS method is developed for the determination of complanatoside A in rat plasma over the range of 2.3–575 ng/mL. Complanatoside A is extracted from plasma by a protein precipitation procedure,separated by LC and detected by MS/MS in positive electrospray ionization mode. The lower limit of quantification is established at 2.3 ng/mL. Intra- and inter-day precisions(LLOQ,low-QC,med-QC and high-QC)are less than 7.9%,and accuracies are between 94.0 and 105.1%. Matrix effect is acceptable(97.9–103.0%)and extraction recovery is reproducible(88.5–94.4%). Complanatoside A is stable in the investigated conditions. The method is applied to the pharmacokinetics of complanatoside A in rats[1].
    动物实验The assay was applied to determine the concentrations of complanatoside A in plasma samples collected from a pharmacokinetic study in rats. Six healthy male Sprague–Dawley rats(200–230 g)were used for the pharmacokinetic study. The rats were housed and handled as reported previously(Guo et al.,2015). The rats were fasted for 12 h before the experiment. Complanatoside A was formulated in water and a single dose of 30 mg/kg was administered by oral gavage. Blood samples were obtained from the vena orbitalis just prior to dose and at 0.083,0.167,0.25,0.5,0.75,1,2,3,5,7,10 and 14 h after administration. After centrifuga_x0002_tion at 6000g for 10 min,the upper plasma was collected and stored at –20°C before analysis.[1]
    数据来源文献[1]. Li N, et al. Quantification of complanatoside A in rat plasma using LC-MS/MS and its application to a pharmacokinetic study. Biomed Chromatogr. 2016 Jun;30(6):888-93.
    单位

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