1. PROTAC Protein Tyrosine Kinase/RTK
  2. PROTACs VEGFR
  3. VEGFR-2-IN-39

VEGFR-2-IN-39 (PROTAC-5) 是靶向 VEGFR-2PROTAC (IC50: 208.6 nM)。VEGFR-2-IN-39 具有低毒性。VEGFR-2-IN-39 浓度依赖性抑制 EA.hy926 (一种 HUVEC) 增殖,IC50 为 38.65 µM。

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VEGFR-2-IN-39 Chemical Structure

VEGFR-2-IN-39 Chemical Structure

CAS No. : 2353417-86-2

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Customer Review

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

VEGFR-2-IN-39 (PROTAC-5) is a PROTAC targeting VEGFR-2 (IC50: 208.6 nM). VEGFR-2-IN-39 has low toxicity.VEGFR-2-IN-39 inhibits the proliferation of EA.hy926, one of HUVECs, in a concentration-dependent manner, with an IC50 of 38.65 µM[1].

IC50 & Target

VEGFR2

 

体外研究
(In Vitro)

VEGFR-2-IN-39(0-60 μM; 0-72 h) 能以剂量依赖的方式有效降低 VEGFR-2 的蛋白质水平[1]
VEGFR-2-IN-39 (10-40 μM; 72 h) 延长 HUVEC 细胞周期的 S 期[1]
VEGFR-2-IN-39 (0.1-40 μM; 72 h),以剂量依赖性方式诱导 HUVEC 细胞凋亡[1]

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

Western Blot Analysis[1]

Cell Line: HUVECs
Concentration: 0-60 μM
Incubation Time: 0-72 h
Result: VEGFR-2 levels by up to 60% at a concentration of 40 μmol/L, with rapid degradation visible as early as 24 hours and nearly complete by 48 hours.

Cell Cycle Analysis[1]

Cell Line: HUVECs
Concentration: 10-40 μM
Incubation Time: 0-72 h
Result: Resulted in a significant increase in the proportion of cells in the S phase, indicating a halt or delay in the progression of the cell cycle. Correspondingly, there was a notable reduction in the number of cells in the G1 phase.

Apoptosis Analysis[1]

Cell Line: HUVECs
Concentration: 0.1-40 μM
Incubation Time: 0-72 h
Result: Resulted in a significant dose-dependent increase in the percentage of apoptotic cells. The percentage of late apoptotic cells increased as follows:
control (untreated) : 5.34%
10 μM: 6.94%
20 μM: 8.32%
30 μM: 15.6%
40 μM: 48.7%
分子量

1000.23

Formula

C55H66FN9O6S

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

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

溶解性数据
In Vitro: 

DMSO 中的溶解度 : 200 mg/mL (199.95 mM; 超声助溶; 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 0.9998 mL 4.9989 mL 9.9977 mL
5 mM 0.2000 mL 0.9998 mL 1.9995 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, 6 months; -20°C, 1 month (protect from light)。-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
参考文献

VEGFR-2-IN-39 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 (protect from light)。-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 0.9998 mL 4.9989 mL 9.9977 mL 24.9943 mL
5 mM 0.2000 mL 0.9998 mL 1.9995 mL 4.9989 mL
10 mM 0.1000 mL 0.4999 mL 0.9998 mL 2.4994 mL
15 mM 0.0667 mL 0.3333 mL 0.6665 mL 1.6663 mL
20 mM 0.0500 mL 0.2499 mL 0.4999 mL 1.2497 mL
25 mM 0.0400 mL 0.2000 mL 0.3999 mL 0.9998 mL
30 mM 0.0333 mL 0.1666 mL 0.3333 mL 0.8331 mL
40 mM 0.0250 mL 0.1250 mL 0.2499 mL 0.6249 mL
50 mM 0.0200 mL 0.1000 mL 0.2000 mL 0.4999 mL
60 mM 0.0167 mL 0.0833 mL 0.1666 mL 0.4166 mL
80 mM 0.0125 mL 0.0625 mL 0.1250 mL 0.3124 mL
100 mM 0.0100 mL 0.0500 mL 0.1000 mL 0.2499 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:
VEGFR-2-IN-39
目录号:
HY-160259
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