MN58b

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MN58b  纯度: 99.17%

MN58b 是一种选择性的 choline kinase α (CHKα) 抑制剂,可抑制磷酸胆碱的合成。MN58b 通过诱导凋亡来减少细胞生长,并具有抗肿瘤活性。

MN58b

MN58b Chemical Structure

CAS No. : 203192-01-2

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MN58b 相关产品

相关化合物库:

  • Bioactive Compound Library Plus

生物活性

MN58b is a selective choline kinase α (CHKα) inhibitor, and results in inhibition of phosphocholine synthesis. MN58b reduces cell growth through the induction of apoptosis, and also has antitumoral activity[1][2].

IC50 & Target

Choline kinase α (CHKα)[1]

体外研究
(In Vitro)

The IC50s of MN58b for parental and Gemcitabine-resistant Suit2 007 cells are 3.14 µM and 0.77 µM, respectively[1].
MN58b (1-5 µM; 72 hours; SK-PC-1, Suit2 008, IMIM-PC2, and RWP-1 cells) has a marked effect on colony formation at 1 µM, and growth is completely abolished at 5 µM in all the cell lines[1].
MN58b ((1-10 µM; 24-48 hours; SK-PC-1, Suit2 008, IMIM-PC2, and RWP-1 cells) induces apoptosis and this response correlates with CHKα expression[1].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[1]

Cell Line: SK-PC-1, Suit2 008, IMIM-PC2, and RWP-1 cells
Concentration: 1 µM, 5 µM
Incubation Time: 72 hours
Result: Inhibited cells growth.

Apoptosis Analysis[1]

Cell Line: SK-PC-1, Suit2 008, IMIM-PC2, and RWP-1 cells
Concentration: 1 µM, 2 µM, 5 µM, 10 µM
Incubation Time: 24 and 48 hours
Result: Induced cell apoptosis.

体内研究
(In Vivo)

MN58b (4 mg/kg; intraperitoneal injection; once a day; for 5 days; MF-1 nude mice) treatment significantly decreases phosphomonoesters in both HT29 and MDA-MB-231 xenografts. Phosphocholine levels are found to correlate with choline kinase activities[2].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: MF-1 nude mice with HT29 or MDA-MB-231 cells[2]
Dosage: 4 mg/kg
Administration: Intraperitoneal injection; once a day; for 5 days
Result: Phosphomonoesters decreased significantly.

分子量

640.49

Formula

C32H40Br2N4

CAS 号

203192-01-2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

溶解性数据
In Vitro: 

DMSO : 14.71 mg/mL (22.97 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 1.5613 mL 7.8065 mL 15.6130 mL
5 mM 0.3123 mL 1.5613 mL 3.1226 mL
10 mM 0.1561 mL 0.7807 mL 1.5613 mL

*

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 (sealed storage, away from moisture)。-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。

In Vivo:

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

  • 1.

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

    Solubility: ≥ 1.47 mg/mL (2.30 mM); Clear solution

    此方案可获得 ≥ 1.47 mg/mL (2.30 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 14.7 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH₂O 中,得到澄清透明的生理盐水溶液

  • 2.

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

    Solubility: ≥ 1.47 mg/mL (2.30 mM); Clear solution

    此方案可获得 ≥ 1.47 mg/mL (2.30 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 14.7 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。

    将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
*以上所有助溶剂都可在 上海金畔生物科技有限公司 网站选购。
参考文献
  • [1]. Mazarico JM, et al. Choline Kinase Alpha (CHKα) as a Therapeutic Target in Pancreatic Ductal Adenocarcinoma: Expression, Predictive Value, and Sensitivity to Inhibitors. Mol Cancer Ther. 2016 Feb;15(2):323-33.

    [2]. Al-Saffar NM, et al. Noninvasive magnetic resonance spectroscopic pharmacodynamic markers of the choline kinase inhibitor MN58b in human carcinoma models. Cancer Res. 2006 Jan 1;66(1):427-34.

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