• 13585831301
  • 021-59541103 021-60443211
  • 3004967995

Fumalic acid

  • 產(chǎn)品貨號(hào):CS-01Y64151
  • 產(chǎn)品價(jià)格:電議
  • 產(chǎn)品產(chǎn)地:進(jìn)口、國(guó)產(chǎn)
  • 包裝類型:10mM (in 1mL DMSO)
  • 采購(gòu)熱度:181
  • 庫(kù)存:100
  • CAS號(hào):1135-24-6
  • 方法:
  • 含量:>98.00%
  • 品牌名稱:莼試
  • 分子式:C10H10O4
  • 分子量:194.18

簡(jiǎn)介內(nèi)容:質(zhì)量保證、價(jià)格優(yōu)惠

在線訂購(gòu)  免費(fèi)訂購(gòu)熱線:021-59541103 021-60443211

標(biāo)簽:Fumalic acid 

產(chǎn)品目錄

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商品詳情購(gòu)物流程代測(cè)服務(wù)付款方式常見(jiàn)問(wèn)題

化學(xué)性質(zhì):                                                                                                             

規(guī)格

10mM (in 1mL DMSO)

CAS

1135-24-6

別名

Coniferic acid

化學(xué)名

(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid

分子式

C10H10O4

分子量

194.18

溶解度

9.45mg/mL in DMSO

儲(chǔ)存條件

Store at 2-8°C

General tips

For obtaining a higher solubility , please warm the tube at 37 and shake it in the ultrasonic bath for a while.

Shipping Condition

Evaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request

 

 

產(chǎn)品描述:                                                                                                             

Ferulic acid is a novel fibroblast growth factor receptor 1 (FGFR1) inhibitor with IC50s of 3.78 and 12.5 μM for FGFR1 and FGFR2, respectively.

Ferulic acid (FA) is a novel fibroblast growth factor receptor 1 (FGFR1) inhibitor with IC50s of 3.78 and 12.5 μM for FGFR1 and FGFR2, respectively. Ferulic acid exhibits great inhibitory activity on FGFR1 with an inhibitory rate of 92% at 1 μM. The proliferation of HUVEC stimulated by FGF1 is markedly decreased after Ferulic acid treatment ranging from 5 to 40 μM for 24 h. Ferulic acid does not exert significant cell viability up to 20 μM, but over 30 μM Ferulic acid exhibits a cytotoxic effect in HUVEC compare to the control. Ferulic acid inhibits FGF1-induced HUVEC migration and invasion in a dose-dependent manner. Ferulic acid markedly suppresses the FGF1-induced phosphorylation of PI3K and Akt. Ferulic acid treatments significantly inhibit MMP-2 and MMP-9 expression stimulated by FGF1[1].

Treatment with Ferulic acid (FA) potently inhibits FGF1-induced neovascularization. It is found that intragastric administration of Ferulic acid markedly inhibits tumor volume and tumor weight, as compare to the counterparts treated with DMSO. Furthermore, Ferulic acid treatment is well tolerated, and there is no significant difference in weight between the vehicle group and the FA-treated groups[1]. Ferulic acid (0.01, 0.1, 1 or 10 mg/kg) given by oral route decreases significantly the immobility time in the forced swimming test (FST) and tail suspension test (TST), whereas produces no effect in the open-field test. Results demonstrate that the administration of Ferulic acid (0.001 mg/kg, p.o.) boosts the antidepressant-like effect of fluoxetine (5 mg/kg, p.o.) in the TST[2].

References:

[1]. Yang GW, et al. Ferulic Acid Exerts Anti-Angiogenic and Anti-Tumor Activity by Targeting Fibroblast Growth Factor Receptor 1-Mediated Angiogenesis. Int J Mol Sci. 2015 Oct 12;16(10):24011-31.

[2]. Zeni AL, et al. Ferulic acid exerts antidepressant-like effect in the tail suspension test in mice: evidence for the involvement of the serotonergic system. Eur J Pharmacol. 2012 Mar 15;679(1-3):68-74.

 

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原創(chuàng)作者:上海莼試生物技術(shù)有限公司

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