Cyasterone
CAS No. 17086-76-9
Cyasterone ( Cyasterone | AI3-44890 | AI3 44890 )
产品货号. M18117 CAS No. 17086-76-9
Cyasterone是一种天然EGFR抑制剂,可通过调节EGFR信号通路抑制A549和MGC823细胞的生长,可能是一种有前途的抗癌化合物。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥518 | 有现货 |
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| 10MG | ¥915 | 有现货 |
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| 25MG | ¥1725 | 有现货 |
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| 50MG | ¥2584 | 有现货 |
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| 100MG | ¥3848 | 有现货 |
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| 200MG | 获取报价 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Cyasterone
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Cyasterone是一种天然EGFR抑制剂,可通过调节EGFR信号通路抑制A549和MGC823细胞的生长,可能是一种有前途的抗癌化合物。
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产品描述Cyasterone was demonstrated potential inhibition effect in skin carcinoma cells.
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体外实验Cyasterone exerts cytotoxicity on multiple cell lines: HeLa (IC50=77.24 μg/ml);HepG-2 (IC50=52.03 μg/ml);MCF-7 (IC50=82.07μg/ml) andMCF-7 (IC50=82.07 μg/ml). And It has none cytotoxicity (IC50>400 μg/ml) on 3 types of carcinoma (HT-29, Caco-2, T47D) and 1 type of normal (NIH 3T3) cell lines.Cyasterone (0-60 μg/ml; 48 hours) causes a significantly decreasing of the cell proliferation. It inhibits cell growth as a dose-dependent manner, exhibits IC50 values of 38.50 μg/ml and 32.96 μg/ml, respectively.Cyasterone (0-60 μg/ml; 24 hours) decreases p-EGFR, p-MEK, and p-mTOR as a dose-dependent manner in A549 cells, it affects the MAPK signaling pathway activities. Cell Viability Assay Cell Line:A549 cells and MGC823 cells Concentration:0 μg/ml, 20 μg/ml, 40 μg/ml, 60 μg/mlIncubation Time:24 hours Result:Inhibited cellproliferation as a dose-dependent manner. Western Blot Analysis Cell Line:A549 cellsConcentration:0 μg/ml, 20 μg/ml, 40 μg/ml, 60 μg/ml Incubation Time:24 hours Result:Surpressed p-EGFR, p-MEK, and p-mTOR expression.
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体内实验Cyasterone (intraperitoneal injection; 5 mg/kg, 10 mg/kg and 15 mg/kg; 21 days) has anti-proliferation effect in vivo and inhibits MGC823 cells xenografted tumor growth in vivo with few changes in body weights. Animal Model:MGC823 xenograft tumor in BALB/C-nu mice Dosage:5 mg/kg, 10 mg/kg and 15 mg/kg Administration:Intraperitoneal injection Result:Inhibited MGC823 xenograft tumor growth in vivo.
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同义词Cyasterone | AI3-44890 | AI3 44890
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通路Others
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靶点Other Targets
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受体EGFR
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研究领域Cancer
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适应症——
化学信息
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CAS Number17086-76-9
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分子量520.66
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分子式C29H44O8
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (192.07 mM)
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SMILESO1C(=O)[C@H]([C@@H]([C@H]1C)C[C@H]([C@@](C)([C@H]1CC[C@]2(C3=CC(=O)[C@@H]4C[C@H]([C@H](C[C@@]4([C@H]3CC[C@]12C)C)O)O)O)O)O)C
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化学全称5-beta-Stigmast-7-en-26-oic acid, 2-beta,3-beta,14,20,22,28-hexahydroxy-6-oxo-, gamma-lactone, (22R,24S,25S,28R)-
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Hirayama Y,et al. Stereochemical assignment of C-24 and C-25 of amarasterone A, a putative biosynthetic intermediate of cyasterone. J Org Chem. 2014 Jun 20;79(12):5471-7.
产品手册
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