1. Protein Tyrosine Kinase/RTK
  2. VEGFR c-Kit PDGFR
  3. Henatinib

Henatinib 是一种口服有效的小分子多激酶抑制剂,具有广泛的抗肿瘤活性。Henatinib 抑制 VEGFR-2c-kitPDGFR 的活性,IC50 值分别为 0.6 nM、3.3 nM 和 41.5 nM。Henatinib 显著抑制人脐静脉内皮细胞 (HUVECs) 中的 VEGFR-2 磷酸化及其下游信号通路。

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Henatinib Chemical Structure

Henatinib Chemical Structure

CAS No. : 1239269-51-2

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  • 生物活性

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  • 参考文献

生物活性

Henatinib is an orally active small-molecule multikinase inhibitor that has demonstrated broad and potent antitumor activities. Henatinib inhibits the activity of VEGFR-2, c-kit, PDGFR with IC50 values of 0.6 nM, 3.3 nM and 41.5 nM, respectively. Henatinib significantly inhibits VEGFR-2 phosphorylation and its downstream signal pathway in human umbilical vein endothelial cells (HUVECs)[1].

IC50 & Target

VEGFR-2

0.6 nM (IC50)

PDGFRα

 

PDGFRβ

 

体外研究
(In Vitro)

Henatinib shows high binding affinities for VEGFRs, PDGFR and stem cell factor receptor[1].
Henatinib significantly inhibits VEGFR-2 phosphorylation and its downstream signal pathway in human umbilical vein endothelial cells (HUVECs), and consistently inhibited VEGF-stimulated HUVEC proliferation, migration and tubule formation[2].

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

Clinical Trial
分子量

468.52

Formula

C25H29FN4O4

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
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  • 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:
Henatinib
目录号:
HY-13645
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