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Ailanthone (AIL) 是一种来自臭椿Ailanthus altissima的天然通过抗肝癌(HCC)成分,可通过降低 cyclins 和 CDKs 的表达、提高 p21 和 p27 的表达来诱导 G0/G1 期细胞周期阻滞。Ailanthone 同时也是一种有效的雄激素受体 (androgen receptor (AR)) 抑制剂,能够抑制完整雄激素受体(IC50:69 nM)、持续活跃剪切变体(IC50:309 nM)
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Ailanthone (AIL) 是一种来自臭椿Ailanthus altissima的天然通过抗肝癌(HCC)成分,可通过降低 cyclins 和 CDKs 的表达、提高 p21 和 p27 的表达来诱导 G0/G1 期细胞周期阻滞。Ailanthone 同时也是一种有效的雄激素受体 (androgen receptor (AR)) 抑制剂,能够抑制完整雄激素受体(IC50:69 nM)、持续活跃剪切变体(IC50:309 nM)
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 313 | 现货 | |
5 mg | ¥ 828 | 现货 | |
10 mg | ¥ 1,490 | 现货 | |
25 mg | ¥ 2,950 | 现货 | |
50 mg | ¥ 4,350 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 913 | 现货 |
产品描述 | Ailanthone (AIL) is a natural compound derived from the tree Ailanthus altissima and has anti-hepatocellular carcinoma (HCC) properties. It can induce G0/G1 phase cell cycle arrest by downregulating the expression of cyclins and CDKs, while upregulating the expression of p21 and p27. Additionally, Ailanthone is a potent androgen receptor (AR) inhibitor, capable of inhibiting both the full-length androgen receptor (IC50: 69 nM) and constitutively active splice variants (IC50: 309 nM). |
靶点活性 | Androgen receptor:69 nM |
体外活性 | Ailanthone通过结合共伴侣蛋白p23,阻止AR与HSP90的相互作用,从而破坏AR-伴侣复合体,进而通过泛素/蛋白酶体介导的途径促进AR以及包括AKT和Cdk4在内的其他p23客户蛋白的降解,下调PCa细胞系和原位动物肿瘤中AR及其靶基因的表达。此外,Ailanthone能够阻断CRPC的肿瘤生长和转移[1]。Ailanthone对包括R-HepG2、Jurkat、HeLa、HepG2、Hep3B、MCF-7、MDA-MB-231及A549细胞在内的多个癌细胞系显示出生长抑制作用。Ailanthone通过诱导线粒体介导的细胞凋亡和G0/G1细胞周期停滞,抑制Huh7细胞生长。Ailanthone诱导的凋亡是线粒体介导的,并在Huh7细胞中涉及PI3K/AKT信号通路[2]。 |
体内活性 | Ailanthone(i.p.或p.o.)在阻断CRPC异种移植瘤生长方面展现出卓越的效能。药动学研究表明,Ailanthone在水中具有良好的溶解度和良好的生物利用度(>20%)。此外,尽管在治疗过程中未达到血浆化合物浓度的稳态,Ailanthone仍有效地抑制CRPC肿瘤生长[1]。 |
细胞实验 | For SRB assay, cells are cultured in complete RPMI 1640 and incubated with indicated concentrations of Ailanthone or cells are maintained in fresh phenol red-free RPMI 1640 medium with 5% charcoal-stripped FBS, 1?nM DHT and indicated compounds. After 48 or 72?h, the cells are then fixed and the cell growth is detected with the SRB assay. For colony formation assay, prostate cancer cells are incubated with indicated concentrations of Ailanthone in complete RPMI 1640 for 2 weeks and then cells are fixed with 4% paraformaldehyde and stained with crystal violet. Colonies are visualized under a microscope, and all of the fields are imaged and counted. Colony formation as a percentage of vehicle control for each cell line is presented [1]. |
动物实验 | In the orthotopic castration-resistant prostate cancer xenografts model, mice are intraperitoneally injected with Ailanthone (2?mg/kg), MDV (10 mg/kg) or DMSO (as controls). Prostate tumor growth and local metastasis are monitored weekly using the IVIS Imaging System. Images and measurements of bioluminescent signals are acquired and analyzed using software [1]. |
别名 | 臭椿酮, Δ13-Dehydrochaparrinone |
分子量 | 376.4 |
分子式 | C20H24O7 |
CAS No. | 981-15-7 |
Smiles | [H][C@]12[C@@]3(O)OC[C@@]11[C@@]([H])(C[C@@]4([H])C(C)=CC(=O)[C@@H](O)[C@]24C)OC(=O)C[C@@]1([H])C(=C)[C@H]3O |
密度 | 1.47g/cm3 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 80 mg/mL (212.54 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
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中药材名称 | 中药材拉丁名 | 性 | 味 | 归经 |
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高樗 | Ailanthus atissima (Mill.)Swingle[Toxicodendron altissima Mill.] | 凉 | 苦 | 肺 |
樗白皮 | Ailanthus altissima(Mill.)Swingle | 寒 | 苦, 涩 | 胃, 大肠 |
椿白皮 | Toona sinensis(A.Juss.)Roem. | 微寒 | 苦, 涩 | 大肠, 胃 |
中成药名称 | 处方组成 | 中成药类型 |
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方剂名称 | 处方组成 | 剂型 | 处方来源 |
---|---|---|---|
椿皮丸2 | 椿白皮,椿白皮 | 丸剂 | 《惠直堂方》卷一。 |
固经汤 | 黄柏,白芍,黄芩,龟板,樗白皮,香附,阿胶,地榆,黄芪 | 汤剂 | 《嵩崖尊生》卷十四。 |
樗白皮汤 | 樗白皮,黄芩,熟地黄,当归,地榆,川芎,芍药,生地黄,伏龙肝,艾叶 | 汤剂 | 《摄生众妙方》卷十。 |
二黄三白汤 | 酒侧柏叶,黄连,黄柏,香附,白石脂,白术,白芍,椿白皮 | 汤剂 | 《妇科玉尺》卷五。 |
荆芥散22 | 荆芥,黄芪,熟地黄,当归,桑耳,地榆,樗白皮,皂荚刺,干姜,槐角,牛蒡子,甘草 | 散剂 | 《圣惠》卷七十二。 |
荆芥穗散 | 荆芥,黄芪,熟地黄,当归,桑耳,地榆,樗白皮,皂角刺,干姜,槐角,牛蒡子,甘草 | 散剂 | 方出《妇人良方》卷八,名见《普济方》卷三二一。 |
金华散1 | 椿白皮,松花 | 散剂 | 《惠直堂方》卷一。 |
樗柏丸 | 樗白皮,黄柏,青黛,干姜,滑石,蛤粉,神曲 | 丸剂 | 《医学入门》卷七。 |
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