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FH535 {[allProObj[0].p_purity_real_show]}

货号:A504800

FH535是一种Wnt/β-catenin和PPAR的抑制剂,具有抗肿瘤活性。

HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
FH535 化学结构 CAS号:108409-83-2
FH535 化学结构
CAS号:108409-83-2
FH535 3D分子结构
CAS号:108409-83-2
FH535 化学结构 CAS号:108409-83-2
FH535 3D分子结构 CAS号:108409-83-2
规格 价格 会员价 库存 数量
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FH535 纯度/质量文件 产品仅供科研

货号:A504800 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 PPARα PPARβ/δ PPARγ PPARδ 其他靶点 纯度
Fenofibric acid 98%
GW6471 ++

PPARα, IC50: 0.24 μM

99%+
GSK3787 ++

PPARδ, pIC50: 6.6

++

PPARδ, pIC50: 6.6

99%+
FH535 98%+
GW9662 +++

PPARα, IC50: 32 nM

+++

PPARγ, IC50: 3.3 nM

98%
T0070907 ++++

PPARγ, IC50: 1 nM

98%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

FH535 生物活性

靶点
  • PPARγ

描述 FH535 is a compound that suppresses both Wnt/beta-catenin and peroxisome proliferator-activated receptor (PPAR) signaling.

FH535 细胞实验

Cell Line
Concentration Treated Time Description References
Caco2 cells 20 µM 2 hours To verify the protective effect of BBR on TNF-α induced TJ damage in Caco2 cells Int J Biol Sci. 2022 Jan 16;18(4):1381-1397.
KYSE-150R cells 20 µM 24 hours FH535 reduced the expression of nuclear β-catenin, reversed EMT phenotypes, and increased the radiosensitivity of KYSE-150R cells. J Transl Med. 2015 Mar 31;13:104.
ARPE-19 cells 0.5 µM 48 hours To assess the impact of FH535 on the activation of EMT; FH535 treatment significantly attenuated the increase of EMT-related markers in TGFβ1-treated ARPE-19 cells. J Neuroinflammation. 2024 Mar 26;21(1):75.
Transformed human hepatocytes (THH) 5 µM 48 hours The combination of AZD5363 and FH535 treatment displays a much greater (~80%) cell death. Cell Death Dis. 2020 Jul 17;11(7):540.
HTR-8/SVneo cells 30 mM 72 hours To investigate the effect of FH535 on glucose uptake and apoptosis in HTR-8/SVneo cells under high glucose conditions. The results showed that FH535 treatment reversed the glucose uptake dysfunction and apoptosis induced by high glucose. Biol Res. 2023 Aug 22;56(1):48.

FH535 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
Mice Laser-induced CNV model Intravitreal injection 0.5 μmol/L Single treatment To evaluate the effect of FH535 on subretinal fibrosis; the area of transformed RPE was reduced by 52.57%. J Neuroinflammation. 2024 Mar 26;21(1):75.

FH535 参考文献

[1]Wachter J, Neureiter D, et al. Influence of five potential anticancer drugs on wnt pathway and cell survival in human biliary tract cancer cells. Int J Biol Sci. 2012;8(1):15-29. Epub 2011 Nov 7.

[2]Handeli S, Simon JA. A small-molecule inhibitor of Tcf/beta-catenin signaling down-regulates PPARgamma and PPARdelta activities. Mol Cancer Ther. 2008 Mar;7(3):521-9.

FH535 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.77mL

0.55mL

0.28mL

13.84mL

2.77mL

1.38mL

27.69mL

5.54mL

2.77mL

FH535 技术信息

CAS号108409-83-2
分子式C13H10Cl2N2O4S
分子量 361.2
SMILES Code O=S(C1=CC(Cl)=CC=C1Cl)(NC2=CC=C([N+]([O-])=O)C=C2C)=O
MDL No. MFCD01212888
别名
运输蓝冰
InChI Key AXNUEXXEQGQWPA-UHFFFAOYSA-N
Pubchem ID 3463933
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Sealed in dry,2-8°C

溶解方案

DMSO: 35 mg/mL(96.9 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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