1. JAK/STAT Signaling Protein Tyrosine Kinase/RTK Apoptosis
  2. EGFR VEGFR Apoptosis
  3. EGFR-IN-174

EGFR-IN-174 是一种有效的 EGFR 抑制剂 (IC50 = 0.17 μM),同时也能够抑制 VEGFR-2 (IC50 = 0.2007 μM)。EGFR-IN-174 具有强效的抗癌作用,且对正常细胞的毒性较低。EGFR-IN-174 可诱导 G2/M 期和 Pre-G1 期细胞阻滞,并显著引发细胞凋亡 (apoptosis)。EGFR-IN-174 可用于癌症相关研究,例如结直肠癌、肝细胞癌和乳腺癌的研究。

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

EGFR-IN-174

EGFR-IN-174 Chemical Structure

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 是否有货
50 mg   询价  
100 mg   询价  
250 mg   询价  

* Please select Quantity before adding items.

Customer Review

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

EGFR-IN-174 is a potent EGFR inhibitor (IC50 = 0.17 μM) and also displays VEGFR-2 inhibition (IC50 = 0.2007 μM). EGFR-IN-174 exhibits potent anticancer effects with low cytotoxicity to normal cells. EGFR-IN-174 induces G2/M and Pre-G1 phase arrest and significantly triggers apoptosis. EGFR-IN-174 can be used in cancer research, such as colorectal carcinoma, hepatocellular carcinoma, and breast cancer[1].

IC50 & Target[1]

VEGFR-2

0.2007 μM (IC50)

体外研究
(In Vitro)

EGFR-IN-174 (compound 3a) (2 天) 对 HCT-116、HepG-2 和 MCF-7 细胞系表现出强细胞毒性 (IC50 值分别为 5.58、4.82 和 11.15 μM),同时对正常 WI-38 细胞表现出极小的细胞毒性 (IC50 = 86.26 μM)[1]
EGFR-IN-174 (4.82-11.15 μM,72 小时) 能有效诱导 HCT-116、HepG-2 和 MCF-7 细胞的 G2/M 期和 Pre-G1 期细胞周期阻滞,并显著触发细胞凋亡[1]

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

Cell Cycle Analysis[1]

Cell Line: HCT-116, HepG-2, and MCF-7 Cells
Concentration: 5.58, 4.82, and 11.15 μM for HCT-116, HepG-2, and MCF-7 Cells, respectively
Incubation Time: 72 h
Result: Induced a significant increase in the Hep-G2 cell population in the G2/M (from 12.73 % to 34.85 %) and Pre-G1 (from 1.92 % to 11.82 %) phases.
Induced a significant increase in the HCT-116 cell population in the G2/M (from 5.45 % to 29.21 %) and Pre-G1 (from 1.91 % to 11.22 %) phases.
Significantly increased the population of MCF-7 Cells in the G2/M and Pre-G1 phases from 9.55 % and 2.14 % to 35.31 % and 15.52 %, respectively.
Reduced the proportion of cells in the G0-G1 and S phases compared to the control in Hep-G2, HCT-116, and MCF-7 cell lines.

Apoptosis Analysis[1]

Cell Line: HCT-116, HepG-2, and MCF-7 Cells
Concentration: 5.58, 4.82, and 11.15 μM for HCT-116, HepG-2, and MCF-7 Cells, respectively
Incubation Time: 72 h
Result: Induced a total apoptosis rate of 11.22 % in HCT-116 cells (early: 3.62 %; late: 6.24 %).
Induced a total apoptosis rate of 11.82 % in HepG-2 cells (early: 3.59 %; late: 6.65 %).
Induced a total apoptosis rate of 15.52 % in MCF-7 cells (early: 4.49 %; late: 8.88 %).
分子量

385.57

Formula

C16H23N3O2S3

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

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

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

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

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
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:
EGFR-IN-174
目录号:
HY-178005
需求量: