2. Protein Tyrosine Kinase/RTK MAPK/ERK Pathway Autophagy
  3. Src p38 MAPK Autophagy
  4. UM-164

UM-164  (Synonyms: DAS-DFGO-II)

目录号: HY-112182 纯度: 99.15%
COA 产品使用指南

摩尔计算器

UM-164 (DAS-DFGO-II) 是一种高效的 c-Src 抑制剂，Kd 为 2.7 nM。UM-164 还高效抑制 p38α 和 p38β 活性。

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UM-164 Chemical Structure

UM-164 Chemical Structure

CAS No. : 903564-48-7

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     可免费申领三个不同产品的试用装。

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规格 价格 是否有货 数量
1 mg ￥323
In-stock
5 mg ￥850
In-stock
10 mg ￥1500
In-stock
50 mg   询价  
100 mg   询价  

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Customer Review

UM-164 相关抗体

Top Publications Citing Use of Products

查看 Src 亚型特异性产品:

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Lck

查看 p38 MAPK 亚型特异性产品:

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p38 MAPK p38α p38β MAPK13 p38δ p38γ

  • 生物活性

  • 实验参考方法

  • 纯度 & 产品资料

  • 参考文献

生物活性

UM-164 (DAS-DFGO-II) is a highly potent inhibitor of c-Src with a Kd of 2.7 nM. UM-164 also potently inhibits p38α and p38β.

IC50 & Target[1]

c-Src

2.7 nM (Kd)

p38α

 

p38β

 

体外研究
(In Vitro)

In biochemical assays, UM-164 is a highly potent inhibitor of c-Src with a binding constant comparable with Dasatinib (UM-164 Kd=2.7 nM, Dasatinib Kd=0.7 nM). To confirm that UM-164 is capable of inhibiting the activation of c-Src in vitro, the effect of UM-164 is examined on the c-Src autophosphorylation in two TNBC cell lines (MDA-MB 231 and SUM 149). Inhibition of c-Src autophosphorylation is detected in a concentration- and a time-dependent manner. At 120 minutes, complete abrogation of c-Src autophosphorylation is observed at 50 nM, demonstrating that UM-164 is a potent c-Src inhibitor in vitro. Flow cytometry experiments demonstrate that UM-164 treatment of MDA-MB 231 and SUM 149 increased the proportion of G0-G1 cells by 25% and 28%, respectively, and concurrently decreased the fraction of S cells by 16% and 19%, respectively[1].

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

UM-164 相关抗体:
体内研究
(In Vivo)

A xenograft study is performed using NCr/nude mice implanted with MDA-MB 231 and SUM 149 cell lines. Once the tumors become palpable, the mice are randomized into control and treatment groups. Mice are injected intraperitoneally with either drug (10 and 20 mg/kg in both xenograft studies; a 15 mg/kg dose is added to the SUM 149 xenograft studies) or vehicle every other day (n=5 for each group). At the selected doses of UM-164, there is no significant weight loss or gross abnormalities observed in the treated animals, even after 52 days of treatment. However, tumor growth is significantly inhibited in both the 10 mg/kg and 20 mg/kg dose groups compared with the vehicle-treated group (P<0.026 and P<0.004, respectively)[1].

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

640.68

Formula

C30H31F3N8O3S
CAS 号
性状

固体

颜色

White to off-white

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
In Vitro: 

DMSO 中的溶解度 : 5 mg/mL (7.80 mM; 超声助溶 (<60°C); 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 1.5608 mL 7.8042 mL 15.6084 mL
5 mM 0.3122 mL 1.5608 mL 3.1217 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

In Vivo:

以下溶解方案，请直接配置工作液。建议现用现配，在短期内尽快用完。 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： 50% PEG300    50% Saline

    Solubility: 5 mg/mL (7.80 mM); 悬浊液; 超声助溶

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

只
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: 99.15%

COA (190 KB) HNMR (285 KB) LCMS (97 KB)

产品使用指南 (1538 KB)
参考文献
Cell Assay
[1]

MDA-MB 231 and SUM 149 cells are plated in triplicate on 60 mm dishes at a density of 1×106 cells/flask. After 24 h, a final concentration of 1 µM UM-164 is added to the cells and incubated for 24 h. Growth medium is then removed and cells are washed with PBS. The remaining cells are trypsinized, harvested, and placed together with growth medium and PBS. Cells are pelleted and re-suspended in 3 mL of 75% ethanol, followed by overnight storage at -20°C. After incubation, cells are centrifuged at 1,500 rpm for 5 min and the cell pellets are re-suspended in 0.05 mg/mL propidium iodide (10 μg/mL) containing 300 μg/mL RNase. Cell clumps are filtered. Cell DNA content is measured on flow cytometer and cell cycle distribution is calculated from 10,000 cells using FACS analysis[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Administration
[1]

Mice[1]
NCr/nude mice, 6 weeks of age, are anesthetized by injecting ketamine:xylazine combination at a concentration of 100 mg/kg:10 mg/kg. A total of 10,000 MDA-MB 231 cells are mixed with Matrigel in a 1:1 ratio by volume and injected into both left and right fourth mammary gland fat pads. Mice are randomized into treatment groups once the tumors are palpable. UM-164 is dissolved in a mixture of DMSO/propylene glycol (1:9). The volume of administration is 0.05 mL/mouse. The control group receive 10 % DMSO/propylene glycol, and the treatment groups receive 10 mg/kg, 15 mg/kg, or 20 mg/kg of UM-164. Mice are treated every other day by intraperitoneal injection, for up to 48 consecutive days. The tumors are monitored twice weekly, and body weight is measured once weekly. Tumor volume is calculated[1].

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

UM-164 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, 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 1.5608 mL 7.8042 mL 15.6084 mL 39.0210 mL
5 mM 0.3122 mL 1.5608 mL 3.1217 mL 7.8042 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.

Keywords:

UM-164903564-48-7DAS-DFGO-IIUM164UM 164Srcp38 MAPKAutophagyInhibitorinhibitorinhibit

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