1. Cell Cycle/DNA Damage Cytoskeleton Autophagy
  2. Microtubule/Tubulin Autophagy
  3. Cabazitaxel

Cabazitaxel  (Synonyms: XRP6258; RPR-116258A; taxoid XRP6258)

目录号: HY-15459 纯度: 99.91%
COA 产品使用指南

Cabazitaxel 是天然紫杉烷脱乙酰基巴卡丁III 的半合成衍生物,具有显著的抗肿瘤功效。

MCE 的所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Cabazitaxel Chemical Structure

Cabazitaxel Chemical Structure

CAS No. : 183133-96-2

1.  客户无需承担相应的运输费用。

2.  同一机构(单位)同一产品试用装仅限申领一次,同一机构(单位)一年内

     可免费申领三个不同产品的试用装。

3.  试用装只面向终端客户

规格 价格 是否有货 数量
10 mM * 1 mL in DMSO ¥550
In-stock
1 mg ¥156
In-stock
5 mg ¥312
In-stock
10 mg ¥500
In-stock
50 mg ¥800
In-stock
100 mg ¥1500
In-stock
500 mg ¥4500
In-stock
1 g   询价  
5 g   询价  

* Please select Quantity before adding items.

Customer Review

Other Forms of Cabazitaxel:

    Cabazitaxel purchased from MCE. Usage Cited in: Prostate. 2018 Feb;78(3):166-177.  [Abstract]

    Western blot analysis of apoptosis marker PARP in stable cell lines treated with 50 or 100 nM Cabazitaxel.

    Cabazitaxel purchased from MCE. Usage Cited in: Oncotarget. 2016 May 17;7(20):28891-902.  [Abstract]

    Western blot analyses for Brachyury and AR expression in prostate cell lines treated with Docetaxel (Doc) or with Cabazitaxel (Cab). Graphs represent the densimetric semi-quantification of western blot images.
    • 生物活性

    • 实验参考方法

    • 纯度 & 产品资料

    • 参考文献

    生物活性

    Cabazitaxel is a semi-synthetic derivative of the natural taxoid 10-deacetylbaccatin III with potential antineoplastic activity.

    细胞效力
    (Cellular Effect)
    Cell Line Type Value Description References
    A-431 GI50
    1.483 nM
    Compound: 3
    Growth inhibition of human A431 cells by MTT assay
    Growth inhibition of human A431 cells by MTT assay
    [PMID: 24405702]
    A549 GI50
    1.483 nM
    Compound: 3
    Growth inhibition of human A549 cells by MTT assay
    Growth inhibition of human A549 cells by MTT assay
    [PMID: 24405702]
    A549 IC50
    15 nM
    Compound: Cabazitaxel
    Cytotoxicity against human A549 cells assessed as inhibition of cell growth measured after 72 hrs by CCK-8 assay
    Cytotoxicity against human A549 cells assessed as inhibition of cell growth measured after 72 hrs by CCK-8 assay
    [PMID: 34058663]
    A549/TR IC50
    62.5 nM
    Compound: Cabazitaxel
    Cytotoxicity against human A549/Taxol cells assessed as inhibition of cell growth measured after 72 hrs by CCK-8 assay
    Cytotoxicity against human A549/Taxol cells assessed as inhibition of cell growth measured after 72 hrs by CCK-8 assay
    [PMID: 34058663]
    BGC-823 GI50
    467.2 nM
    Compound: 3
    Growth inhibition of human BGC823 cells by MTT assay
    Growth inhibition of human BGC823 cells by MTT assay
    [PMID: 24405702]
    DU-145 GI50
    1.429 nM
    Compound: 3
    Growth inhibition of human DU145 cells by MTT assay
    Growth inhibition of human DU145 cells by MTT assay
    [PMID: 24405702]
    HeLa GI50
    1.799 nM
    Compound: 3
    Growth inhibition of human HeLa cells by MTT assay
    Growth inhibition of human HeLa cells by MTT assay
    [PMID: 24405702]
    HL-60 GI50
    4.736 nM
    Compound: 3
    Growth inhibition of human HL60 cells by MTT assay
    Growth inhibition of human HL60 cells by MTT assay
    [PMID: 24405702]
    HT-1080 GI50
    1.406 nM
    Compound: 3
    Growth inhibition of human HT1080 cells by MTT assay
    Growth inhibition of human HT1080 cells by MTT assay
    [PMID: 24405702]
    K562 GI50
    4.186 nM
    Compound: 3
    Growth inhibition of human K562 cells by MTT assay
    Growth inhibition of human K562 cells by MTT assay
    [PMID: 24405702]
    KB IC50
    20 nM
    Compound: Cabazitaxel
    Cytotoxicity against human KB cells assessed as inhibition of cell growth measured after 72 hrs by CCK-8 assay
    Cytotoxicity against human KB cells assessed as inhibition of cell growth measured after 72 hrs by CCK-8 assay
    [PMID: 34058663]
    MCF7 GI50
    1.187 nM
    Compound: 3
    Growth inhibition of human MCF7 cells by MTT assay
    Growth inhibition of human MCF7 cells by MTT assay
    [PMID: 24405702]
    MES-SA/Dx5 IC50
    15 nM
    Compound: Cabazitaxel
    Growth inhibition of human MES-SA/Dx5 cells after 72 hrs by SRB assay
    Growth inhibition of human MES-SA/Dx5 cells after 72 hrs by SRB assay
    [PMID: 29251920]
    NCI-H524 IC50
    0.26 nM
    Compound: Cabazitaxel
    Cytotoxicity in human NCI-H524 cells pre-incubated for 2 hrs followed by compound wash out and subsequently incubated for 70 hrs by Cell Titer Glo assay
    Cytotoxicity in human NCI-H524 cells pre-incubated for 2 hrs followed by compound wash out and subsequently incubated for 70 hrs by Cell Titer Glo assay
    [PMID: 30735385]
    PANC-1 GI50
    1.283 nM
    Compound: 3
    Growth inhibition of human PANC1 cells by MTT assay
    Growth inhibition of human PANC1 cells by MTT assay
    [PMID: 24405702]
    SGC-7901 GI50
    0.3553 nM
    Compound: 3
    Growth inhibition of human SGC7901 cells by MTT assay
    Growth inhibition of human SGC7901 cells by MTT assay
    [PMID: 24405702]
    U-937 GI50
    0.5391 nM
    Compound: 3
    Growth inhibition of human U937 cells by MTT assay
    Growth inhibition of human U937 cells by MTT assay
    [PMID: 24405702]
    体外研究
    (In Vitro)

    The cytotoxicity of cabazitaxel (100 μg/mL) on 4T1 cells without irradiation is 70.8%. Cabazitaxel (100 μg/mL) exhibits a concentration-dependent antiproliferation effect, with the antiproliferative activity of 56.2%[1].

    MCE has not independently confirmed the accuracy of these methods. They are for reference only.

    体内研究
    (In Vivo)

    Cabazitaxel (10 mg/kg, i.v.) has certain toxicity to liver and kidney but it can be avoided by integrated into Ans. The body weights of mice treated with AN-ICG-CBX and AN-CBX have a slightly decrease, while body weights of the free CBX group significantly decrease compared to the control group[1].

    MCE has not independently confirmed the accuracy of these methods. They are for reference only.

    Clinical Trial
    分子量

    835.93

    Formula

    C45H57NO14

    CAS 号
    性状

    固体

    颜色

    White to off-white

    结构分类
    初始来源
    运输条件

    Room temperature in continental US; may vary elsewhere.

    储存方式
    Powder -20°C 3 years
    4°C 2 years
    In solvent -80°C 2 years
    -20°C 1 year
    溶解性数据
    细胞实验: 

    DMSO 中的溶解度 : ≥ 100 mg/mL (119.63 mM; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

    * "≥" means soluble, but saturation unknown.

    配制储备液
    浓度 溶剂体积 质量 1 mg 5 mg 10 mg
    1 mM 1.1963 mL 5.9814 mL 11.9627 mL
    5 mM 0.2393 mL 1.1963 mL 2.3925 mL
    查看完整储备液配制表

    * 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
    储备液的保存方式和期限:-80°C, 2 years; -20°C, 1 year。-80°C储存时,请在2年内使用, -20°C储存时,请在1年内使用。

    • 摩尔计算器

    • 稀释计算器

    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

    质量
    =
    浓度
    ×
    体积
    ×
    分子量 *

    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

    浓度 (start)

    C1

    ×
    体积 (start)

    V1

    =
    浓度 (final)

    C2

    ×
    体积 (final)

    V2

    动物实验:

    请根据您的 实验动物和给药方式 选择适当的溶解方案。

    以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:
    ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用
    以下溶剂前显示的百分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

    • 方案 一

      请依序添加每种溶剂: 10% DMSO    40% PEG300    5% Tween-80    45% Saline

      Solubility: ≥ 2.5 mg/mL (2.99 mM); 澄清溶液

      此方案可获得 ≥ 2.5 mg/mL(饱和度未知)的澄清溶液。

      1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;再向上述体系中加入 50 μL Tween-80,混合均匀;然后再继续加入 450 μL 生理盐水 定容至 1 mL

      生理盐水的配制:将 0.9 g 氯化钠,溶解于 ddH₂O 并定容至 100 mL,可以得到澄清透明的生理盐水溶液。
    • 方案 二

      请依序添加每种溶剂: 10% DMSO    90% (20% SBE-β-CD in Saline)

      Solubility: ≥ 2.5 mg/mL (2.99 mM); 澄清溶液

      此方案可获得 ≥ 2.5 mg/mL(饱和度未知)的澄清溶液。

      1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液 中,混合均匀。

      2 g SBE-β-CD(磺丁基醚 β-环糊精)粉末定容于 10 mL 的生理盐水中,完全溶解至澄清透明。
    动物溶解方案计算器
    请输入动物实验的基本信息:

    给药剂量

    mg/kg

    动物的平均体重

    g

    每只动物的给药体积

    μL

    动物数量

    由于实验过程有损耗,建议您多配一只动物的量
    请输入您的动物体内配方组成:
    %
    DMSO +
    +
    %
    Tween-80 +
    %
    Saline
    如果您的动物是免疫缺陷鼠或者体弱鼠,建议 DMSO 中的在最后工作液体系中的占比尽量不超过 2%。
    方案所需 助溶剂 包括:DMSO ,均可在 MCE 网站选购。 Tween 80,均可在 MCE 网站选购。
    计算结果
    工作液所需浓度 : mg/mL
    储备液配制方法 : mg 药物溶于 μL  DMSO(母液浓度为 mg/mL)。
    您所需的储备液浓度超过该产品的实测溶解度,以下方案仅供参考,如有需要,请与 MCE 中国技术支持联系。
    动物实验体内工作液的配制方法 : 取 μL DMSO 储备液,加入 μL  μL ,混合均匀至澄清,再加 μL Tween 80,混合均匀至澄清,再加 μL 生理盐水
    连续给药周期超过半月以上,请谨慎选择该方案。
    请确保第一步储备液溶解至澄清状态,从左到右依次添加助溶剂。您可采用超声加热 (超声清洗仪,建议频次 20-40 kHz),涡旋吹打等方式辅助溶解。
    纯度 & 产品资料

    纯度: 99.96%

    参考文献
    Cell Assay
    [1]

    The cytotoxicity of CBX-loaded ANs and free Cabazitaxel (CBX) is evaluated with MTT assay. Cells are seeded onto a 96-well plate at a density of 3000 cells per well and cultured for 24 h. CBX-loaded ANs and free CBX are diluted to predetermined concentrations with PBS and added into each well. Blank AN, AN-ICG and free CBX solvent (a mixture of Tween-80 and anhydrous alcohol) are added as well to different final concentrations. The incubation continued for another 48 hours. 20 µL MTT solutions (5 mg/mL in PBS) are added into each well and cells are incubated for another 4 hours under 37°C. Subsequently the medium is removed and 150 µL dimethyl sulphoxide (DMSO) is added to dissolve the purple formazan salt crystals. Then the absorbance is measured by a microplate reader at 490 nm. The cells treated with medium are evaluated as controls.

    MCE has not independently confirmed the accuracy of these methods. They are for reference only.

    Animal Administration
    [1]

    To evaluate the antitumor efficiency of the combined chemotherapy and PTT in vivo, mice bearing 4T1 tumor are randomLy divided into 6 treatment groups (n=5). Treatment begin when the tumors reached 50 mm3-100 mm3. The mice are intravenously injected with saline, AN-ICG, free Cabazitaxel (CBX), AN-CBX and AN-ICG-CBX (ICG 2 mg/kg, CBX 10 mg/kg). 8 hours later, the groups injected with AN-ICG and AN-ICG-CBX is irradiated by the 808 nm laser (0.8 W/cm2, 5 min). The length and width of every tumor are measured by a caliper every other day. The formula (volume (mm3) =1/2 × length × width2) is used to calculate the tumor volume. The body weights of these mice are recorded every two days using an electronic balance as well. At the end of the antitumor study, the 4T1 tumor bearing mice are sacrificed to collect the tumors and major organs.

    MCE has not independently confirmed the accuracy of these methods. They are for reference only.

    参考文献

    完整储备液配制表

    * 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
    储备液的保存方式和期限:-80°C, 2 years; -20°C, 1 year。-80°C储存时,请在2年内使用, -20°C储存时,请在1年内使用。

    可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
    DMSO 1 mM 1.1963 mL 5.9814 mL 11.9627 mL 29.9068 mL
    5 mM 0.2393 mL 1.1963 mL 2.3925 mL 5.9814 mL
    10 mM 0.1196 mL 0.5981 mL 1.1963 mL 2.9907 mL
    15 mM 0.0798 mL 0.3988 mL 0.7975 mL 1.9938 mL
    20 mM 0.0598 mL 0.2991 mL 0.5981 mL 1.4953 mL
    25 mM 0.0479 mL 0.2393 mL 0.4785 mL 1.1963 mL
    30 mM 0.0399 mL 0.1994 mL 0.3988 mL 0.9969 mL
    40 mM 0.0299 mL 0.1495 mL 0.2991 mL 0.7477 mL
    50 mM 0.0239 mL 0.1196 mL 0.2393 mL 0.5981 mL
    60 mM 0.0199 mL 0.0997 mL 0.1994 mL 0.4984 mL
    80 mM 0.0150 mL 0.0748 mL 0.1495 mL 0.3738 mL
    100 mM 0.0120 mL 0.0598 mL 0.1196 mL 0.2991 mL
    Help & FAQs
    • Do most proteins show cross-species activity?

      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

    您最近查看的产品:

    Your information is safe with us. * Required Fields.

       产品名称:

     

    * 需求量:

    * 客户姓名:

     

    * Email:

    * 电话:

     

    * 公司或机构名称:

       留言给我们:

    Bulk Inquiry

    Inquiry Information

    产品名称:
    Cabazitaxel
    目录号:
    HY-15459
    需求量: