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防己诺林碱 /Fangchinoline {[allProObj[0].p_purity_real_show]}

货号:A334684 同义名: 防己醇灵 / 7-O-Demethyltetrandrine;NSC 77036

Fangchinoline is an isolate of Stephania tetrandra and has anticancer activity through induction of G1 arrest in breast cancer cells.

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+
Fangchinoline 化学结构 CAS号:436-77-1
Fangchinoline 化学结构
CAS号:436-77-1
Fangchinoline 3D分子结构
CAS号:436-77-1
Fangchinoline 化学结构 CAS号:436-77-1
Fangchinoline 3D分子结构 CAS号:436-77-1
规格 价格 会员价 库存 数量
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Fangchinoline 纯度/质量文件 产品仅供科研

货号:A334684 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 FAK 其他靶点 纯度
Defactinib 99%+
NVP-TAE 226 ++

PYK2, IC50: 3.5 nM

FAK, IC50: 5.5 nM

Insulin Receptor,IGF-1R 98+%
PF-573228 +

FAK, IC50: 4 nM

98%
Solanesol 90% +(HPLC)
PF-431396 ++

PYK2, IC50: 11 nM

FAK, IC50: 2 nM

99%+
PND-1186 ++++

FAK, IC50: 1.5 nM

99%+
PF-562271 ++++

PYK2, IC50: 13 nM

FAK, IC50: 1.5 nM

99%+
GSK2256098 ++++

FAK, Ki: 0.4 nM

99%+
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。

Fangchinoline 生物活性

描述 Fangchinoline, as a natural product, has the characteristics of enhancing immune function, low toxicity and good liver protection features. Fangchinoline inhibited the proliferation of A375 and A875 cells activity with IC50 values of 12.41 and 16.20 µM. Fangchinoline significantly decreased the invasion and migration potential of A375 cells and A875 cells in a dose-dependent manner [3]. Fangchinoline inhibited the growth of MDA-MB-231 cells in concentration-dependent manner and it induced MDA-MB-231 cell apoptosis[4]. In addition, fangchinoline suppressed the growth of subcutaneous osteosarcoma tumors in Balb/c mice subcutaneously injected with osteosarcoma cells[5].

Fangchinoline 参考文献

[1]Guo B, Su J, et al. Fangchinoline as a kinase inhibitor targets FAK and suppresses FAK-mediated signaling pathway in A549. J Drug Target. 2015 Apr;23(3):266-74.

[2]Wang CD, Yuan CF, et al. Fangchinoline inhibits cell proliferation via Akt/GSK-3beta/ cyclin D1 signaling and induces apoptosis in MDA-MB-231 breast cancer cells. Asian Pac J Cancer Prev. 2014;15(2):769-73.

[3]Shi J, Guo B, Hui Q, Chang P, Tao K. Fangchinoline suppresses growth and metastasis of melanoma cells by inhibiting the phosphorylation of FAK. Oncol Rep. 2017 Jul;38(1):63-70. doi: 10.3892/or.2017.5678. Epub 2017 May 30. PMID: 28560386; PMCID: PMC5492563.

[4]Wang B, Xing Z, Wang F, Yuan X, Zhang Y. Fangchinoline inhibits migration and causes apoptosis of human breast cancer MDA-MB-231 cells. Oncol Lett. 2017 Nov;14(5):5307-5312. doi: 10.3892/ol.2017.6831. Epub 2017 Aug 25. PMID: 29098027; PMCID: PMC5652195.

[5]Li X, Yang Z, Han W, Lu X, Jin S, Yang W, Li J, He W, Qian Y. Fangchinoline suppresses the proliferation, invasion and tumorigenesis of human osteosarcoma cells through the inhibition of PI3K and downstream signaling pathways. Int J Mol Med. 2017 Aug;40(2):311-318. doi: 10.3892/ijmm.2017.3013. Epub 2017 Jun 6. PMID: 28586029; PMCID: PMC5504998.

Fangchinoline 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.64mL

0.33mL

0.16mL

8.21mL

1.64mL

0.82mL

16.43mL

3.29mL

1.64mL

Fangchinoline 技术信息

CAS号436-77-1
分子式C37H40N2O6
分子量 608.723
别名 防己醇灵 ;7-O-Demethyltetrandrine;NSC 77036;Hanfangchin B
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Keep in dark place,Inert atmosphere,2-8°C

溶解度

DMSO: 50 mg/mL(82.14 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

动物实验配方
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