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Ailanthone {[allProObj[0].p_purity_real_show]}

货号:A619453 同义名: Δ13-Dehydrochaparrinone;AIL

Ailanthone, a natural product isolated and purified from the barks of Ailanthus altissima with high toxicity, has significant pre-emergence herbicide activity directly correlated to its concentration.

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+
Ailanthone 化学结构 CAS号:981-15-7
Ailanthone 化学结构
CAS号:981-15-7
Ailanthone 3D分子结构
CAS号:981-15-7
Ailanthone 化学结构 CAS号:981-15-7
Ailanthone 3D分子结构 CAS号:981-15-7
规格 价格 会员价 库存 数量
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Ailanthone 纯度/质量文件 产品仅供科研

货号:A619453 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 Androgen Receptor 其他靶点 纯度
Cyproterone acetate ++++

Androgen Receptor, IC50: 7.1 nM

98%
Apalutamide +++

Androgen Receptor, IC50: 16 nM

98%
AZD3514 +

Androgen Receptor, Ki: 2.2 μM

98%
Darolutamide ++++

Androgen receptor, Ki: 11 nM

98%
Flutamide +++

Androgen Receptor, Ki: 55 nM

98%
Galeterone ++

Androgen Receptor, IC50: 384 nM

98%
Enzalutamide +++

Androgen Receptor, IC50: 36 nM

98%
Megestrol 98%
Bicalutamide ++

Androgen Receptor, IC50: 0.16 μM

99%
EPI-001 +

Androgen Receptor, IC50: ~6 μM

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。

Ailanthone 生物活性

靶点
  • PI3K

描述 Ailanthone (Δ13-Dehydrochaparrinone) is a potent inhibitor of both full-length androgen receptor (AR) (IC50=69 nM) and constitutively active truncated AR splice variants (AR1-651 IC50=309 nM)[3]. Ailanthone triggered DNA damage characterized by activation of the ATM/ATR pathway. Moreover, ailanthone-induced cell death was associated with apoptosis, as evidenced by an increased ratio of cells in the subG1 phase and by PARP cleavage and caspase activation. Ailanthone inhibited the growth and angiogenesis of tumor xenografts without significant secondary adverse effects, indicating its safety for treating HCC (anti-hepatocellular carcinoma)[4]. Ailanthone induces cell cycle arrest via the PI3K-Akt signaling pathway as well as cell apoptosis via the mitochondria-mediated apoptotic signaling pathway[5]. AIL (Ailanthone) suppresses the activity of colon cancer cells via the STAT3 pathway[6].

Ailanthone 参考文献

[1]Pedersini C, Bergamin M, et al. Herbicide activity of extracts from Ailanthus altissima (Simaroubaceae). Nat Prod Commun. 2011 May;6(5):593-6.

[2]Kato T, Suzumura Y, et al. Antitumor activity of novel ailanthone derivatives in vitro and in vivo. Anticancer Res. 1988 Jul-Aug;8(4):573-9.

[3]He Y, Peng S, Wang J, Chen H, Cong X, Chen A, Hu M, Qin M, Wu H, Gao S, Wang L, Wang X, Yi Z, Liu M. Ailanthone targets p23 to overcome MDV3100 resistance in castration-resistant prostate cancer. Nat Commun. 2016 Dec 13;7:13122

[4]Zhuo Z, Hu J, Yang X, Chen M, Lei X, Deng L, Yao N, Peng Q, Chen Z, Ye W, Zhang D. Ailanthone Inhibits Huh7 Cancer Cell Growth via Cell Cycle Arrest and Apoptosis In Vitro and In Vivo. Sci Rep. 2015 Nov 3;5:16185

[5]Liu W, Liu X, Pan Z, Wang D, Li M, Chen X, Zhou L, Xu M, Li D, Zheng Q. Ailanthone Induces Cell Cycle Arrest and Apoptosis in Melanoma B16 and A375 Cells. Biomolecules. 2019 Jul 11;9(7):275

[6]Ding H, Yu X, Yan Z. Ailanthone suppresses the activity of human colorectal cancer cells through the STAT3 signaling pathway. Int J Mol Med. 2022 Feb;49(2):21

Ailanthone 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.66mL

0.53mL

0.27mL

13.28mL

2.66mL

1.33mL

26.57mL

5.31mL

2.66mL

Ailanthone 技术信息

CAS号981-15-7
分子式C20H24O7
分子量 376.4
别名 Δ13-Dehydrochaparrinone;AIL;Δ13-Dehydrochaparrinone, Ailanthone
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Sealed in dry,Store in freezer, under -20°C

溶解度

DMSO: 50 mg/mL(132.84 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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