
Polyphyllin I
CAS No. 50773-41-6
Polyphyllin I ( —— )
产品货号. M18674 CAS No. 50773-41-6
Polyphyllin D 通过线粒体凋亡途径诱导细胞凋亡,具体表现为 Bcl-2 表达水平降低、MMP 破坏以及 Bax、细胞色素 C 和 cleaved-caspase-3 水平升高。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥421 | 有现货 |
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10MG | ¥721 | 有现货 |
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25MG | ¥1239 | 有现货 |
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50MG | ¥1928 | 有现货 |
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100MG | ¥3216 | 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Polyphyllin I
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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Polyphyllin D 通过线粒体凋亡途径诱导细胞凋亡,具体表现为 Bcl-2 表达水平降低、MMP 破坏以及 Bax、细胞色素 C 和 cleaved-caspase-3 水平升高。
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产品描述Polyphyllin D induces apoptosis via the mitochondrial apoptotic pathway as evidenced by decreased Bcl-2 expression levels, disruption of MMP and increased Bax, cytochrome C, and cleaved-caspase-3 levels. Polyphyllin D has an anti-angiogenic effect. Polyphyllin D has toxicity in human RBCs as well as its underlying mechanism for the hemolysis and eryptosis/erythroptosis. Polyphyllin D has strong anticancer activity, can overcome drug resistance in R-HepG2 cells and elicit programmed cell death via mitochondrial dysfunction.
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体外实验Cell Proliferation Assay Cell Line:A549, H460, and SK-MES-1 cells Concentration:24, 48, 72 hours Incubation Time:24, 48, 72 hours Result:Markedly reduced proliferation capacity in vitro and in a concentration-dependent manner.
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体内实验Animal Model:BALB/c nude mice (5 weeks old) were s.c. inoculated with A549 cells Dosage:1.5 mg/kg Administration:I.p. twice daily from day 2 to day 11 Result:The tumor growth rate was much lower than that in cisplatin group and PBS group.
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同义词——
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通路Apoptosis
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靶点NF-κB
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受体Others
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研究领域Others-Field
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适应症——
化学信息
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CAS Number50773-41-6
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分子量855.03
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分子式C44H70O16
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (116.96 mM)
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SMILES[C@@H]1([C@@H]([C@@H]([C@H]([C@@H](O1)C)O)O)O)O[C@H]1[C@@H](O[C@@H]([C@H]([C@@H]1O)O[C@@H]1O[C@H]([C@@H]([C@H]1O)O)CO)CO)O[C@@H]1CC2=CC[C@H]3[C@@H]4C[C@@H]5O[C@@]6([C@H]([C@@H]5[C@]4(CC[C@@H]3[C@]2(CC1)C)C)C)CC[C@H](CO6)C
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化学全称——
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. Wu L,et al. Polyphyllin D induces apoptosis in K562/A02 cells through G2/M phase arrest.Wu L1, Li Q, Liu Y.J Pharm Pharmacol. 2014 May;66(5):713-21.
产品手册




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