1. Apoptosis Epigenetics
  2. Apoptosis SF3B1
  3. Pladienolide B

Pladienolide B 是一种有效的癌细胞生长抑制剂,其作用靶向剪接体的 SF3B1 亚单位。Pladienolide B 通过抑制前 mRNA 剪接发挥抗肿瘤作用,诱导调亡。

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Pladienolide B Chemical Structure

Pladienolide B Chemical Structure

CAS No. : 445493-23-2

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规格 价格 是否有货 数量
100 μg ¥4200
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Customer Review

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Pladienolide B is a potent cancer cell growth inhibitor that targets the SF3B1 subunit of the spliceosome. Pladienolide B exerts antitumor activities mediated through the inhibition of pre-mRNA splicing. Pladienolide B induces apoptosis[1][2][3].

体外研究
(In Vitro)

Pladienolide B (0.1-2 nM; 24-72 hours) inhibits human cervical carcinoma cells viability[3].
Pladienolide B (0.1-2 nM; 24-48 hours) reduces SF3b1 expression in human cervical carcinoma cells[3].
Pladienolide B induces (0.1-2 nM; 24 hours) cell cycle arrest and apoptosis[3].

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

Cell Viability Assay[3]

Cell Line: HeLa cells
Concentration: 0.1, 0.5, 1, 1.5, 2 nM
Incubation Time: 24, 48, 72 hours
Result: Significantly decreased cell viability, and the decrease was concentration- and time-dependent.

Apoptosis Analysis[3]

Cell Line: HeLa cells
Concentration: 0.1, 0.5, and 2 nM
Incubation Time: 24 hours
Result: The apoptotic cells were highly induced at 24 hours.

RT-PCR[3]

Cell Line: HeLa cells
Concentration: 0.1, 0.5, and 2 nM
Incubation Time: 24, 48 hours
Result: Induced a time- and concentration-dependent decrease in cellular SF3b1 proteins.
体内研究
(In Vivo)

Pladienolide B (2.5-10 mg/kg; i.v.; daily for 5 days) has strong antitumor activities[4].

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

Animal Model: Female or male BALB/c nu/nu mice (7 weeks of age) (PC-3, OVCAR-3, DU-145, WiDr, and HCT-116, BSY-1 xenografts)[4]
Dosage: 2.5, 5, and 10 mg/kg
Administration: I.v.; daily for 5 days
Result: Showed strong growth inhibitory or regressive activities against these xenografts.
分子量

536.70

Formula

C30H48O8

CAS 号
性状

油状物

颜色

Colorless to light yellow

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Pure form -20°C 3 years
In solvent -80°C 6 months
-20°C 1 month
溶解性数据
In Vitro: 

DMSO 中的溶解度 : 1 mg/mL (1.86 mM; 超声加热助溶; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 1.8632 mL 9.3162 mL 18.6324 mL
5 mM --- --- ---
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, 6 months; -20°C, 1 month。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

  • 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
计算结果
工作液所需浓度 : mg/mL
纯度 & 产品资料

纯度: ≥99.0%

参考文献

Pladienolide B 相关分类

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, 6 months; -20°C, 1 month。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 1.8632 mL 9.3162 mL 18.6324 mL 46.5810 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.

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产品名称:
Pladienolide B
目录号:
HY-16399
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