1. Protein Tyrosine Kinase/RTK Stem Cell/Wnt MAPK/ERK Pathway
  2. VEGFR ERK
  3. EVT801

EVT801 是一种口服有效、选择性的 VEGFR-3 抑制剂 (IC50=11 nM),具有抗肿瘤作用。EVT801 不仅抑制 VEGF-C 诱导的人内皮细胞增殖,还抑制肿瘤小鼠模型中的肿瘤 (淋巴) 血管生成。EVT801 能够减少肿瘤缺氧,减少免疫抑制细胞因子 (CCL4、CCL5) 和髓系衍生抑制细胞 (MDSC) 产生。EVT801 与免疫检查点疗法 (ICT) 组有协同作用,它提高 ICT 应答率,对癌小鼠模型的抑制效果更好。

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EVT801 Chemical Structure

EVT801 Chemical Structure

CAS No. : 1412453-70-3

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规格 价格 是否有货 数量
5 mg ¥9800
10 - 12 周
10 mg   询价  
50 mg   询价  

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

EVT801 is an orally active and selective inhibitor of VEGFR-3 (IC50=11 nM), which has antitumor effects. EVT801 inhibits not only VEGF-C-induced human endothelial cell proliferation, but also tumor (lymphatic) angiogenesis in tumor mouse models. EVT801 can reduce tumor hypoxia, immunosuppressive cytokines (CCL4, CCL5) and myeloid derived suppressor cells (MDSC) production. EVT801 has synergistic effect with immune checkpoint therapy (ICT), which improves ICT response rate and has better inhibitory effect on cancer mouse models[1]. EVT801 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

IC50 & Target[1]

VEGFR3

11 nM (IC50)

VEGFR1

396 nM (IC50)

VEGFR2

130 nM (IC50)

ERK

13 nM (IC50)

体外研究
(In Vitro)

EVT801 (10 nM-1 μM) dose-dependently inhibits VEGFR-1/2/3 autophosphorylation in HEK293 cells with IC50s of 39 nM (VEGFR-3), 2130 nM (VEGFR-1), 260 nM (VEGFR-2), respectively[1].
EVT801 (1 nM-1 μM) prevents proliferation of VEGFR-3-positive cells, human lymphatic microvascular endothelial cells (hLMVEC) for example. EVT801 inhibits the induction of hLMVECs proliferation dose-dependently with IC50s of 15 nM (VEGF-C), 8 nM (VEGF-D), 155 nM (VEGF-A), respectively[1].
EVT801 (1 μM) inhibits proliferation and tumor growth of VEGFR-3-positive tumor cells[1].

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

Cell Proliferation Assay[1]

Cell Line: VEGFR-3-positive cells, human lymphatic microvascular endothelial cells (hLMVEC)
Concentration: 1 nM-1 μM
Incubation Time:
Result: Showed a maximum inhibition of 74%, 100%, and 65% against VEGF-C, VEGF-D, VEGF-A induction, respectively.
体内研究
(In Vivo)

EVT801 (30 mg/kg; p.o.; twice daily for 7 d) shows inhibitory effect on VEGFR-3-positive tumors in mouse models, such as RT-001-HAM Subcutaneous Patient-derived xenograft (PDx) Tumor Mouse Model, 4T1 Mammary Carcinoma Mouse Model, N-diethylnitrosamine-Induced Hepatocarcinoma Mouse Model, NCI-H1703 Subcutaneous Xenograft Tumor Mouse Model, Rip1-Tag2/transgenic Mouse Models, and CT26 Ectopic Tumor Mouse Model. EVT801 is expressed in blood vessels of kidney cancer primary tumors and metastases, and in tumor cells of endothelial malignancies[1].

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

Clinical Trial
分子量

367.40

Formula

C19H21N5O3

CAS 号
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

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

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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:
EVT801
目录号:
HY-152293
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