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- 文献和实验
- 技术资料
- 英文名:
(5R,5aR,8aR,9S)-9-(((2R,4aR,6R,7R,8R,8aS)-7,8-Dihydroxy-2-(thiophen-2-yl)hexahydropyrano[3,2-d][1,3]dioxin-6-yl)oxy)-5-(4-hydroxy-3,5-dimethoxyphenyl)-5,5a,8a,9-tetrahydrofuro[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6(8H)-one
- 供应商:
上海安毕达生物科技有限公司
- CAS号:
29767-20-2
- 规格:
50μL/1mL/5mg/10mg/25mg/50mg/100mg
| 规格: | 50μL | 产品价格: | ¥119.0 |
|---|---|---|---|
| 规格: | 1mL | 产品价格: | ¥508.0 |
| 规格: | 5mg | 产品价格: | ¥173.0 |
| 规格: | 10mg | 产品价格: | ¥278.0 |
| 规格: | 25mg | 产品价格: | ¥528.0 |
| 规格: | 50mg | 产品价格: | ¥920.0 |
| 规格: | 100mg | 产品价格: | ¥1280.0 |
Type II topoisomerases are ubiquitous enzymes in all branches of life that can alter DNA superhelicity and unlink double-stranded DNA segments during processes such as replication and transcription. In cells, type II topoisomerases are particularly useful for their ability to disentangle newly-replicated sister chromosomes3. Teniposide is a topoisomerase II inhibitor. Teniposide (VM-26, 0.15-45 mg/L) inhibits the proliferation of Tca8113 cells in a dose-dependent manner, with an IC50 of 0.35 mg/L. Teniposide (5 mg/L) induces apoptosis of Tca8113 cells. Teniposide (5.0 mg/L) causes cell arrested at G2/M phase in Tca8113 cells4.Teniposide (0.5 mg/kg, i.p.) significantly increases micronucleated polychromatic erythrocyte (MNPCE) frequencies, which is directly related to bone marrow toxicity as significant suppression of bone marrow is noted. Teniposide (24 mg/kg, i.p.) markedly decreases the frequencies of BrdU-labelled sperm. Teniposide (12, 24 mg/kg, i.p.) also dramatically induces disomic sperm in the germ cell of male mice5. Teniposide is active on primary cultured glioma cells from patients, when the level of miR-181b is high in the cells, with an IC50 of 1.3 ± 0.34 μg/mL. Cells treated with teniposide with low MDM2 have decreased viability compared with control cells, and the IC50 decreases from 5.86 ± 0.36 μg/mL to 2.90 ± 0.35 μg/mL upon MDM2 suppression. Teniposide also inhibits the viability of glioma cell with high level of miR-181b, through mediation of MDM26.
溶解方案(细胞实验)
DMSO 中的溶解度 : ≥ 30 mg/mL (45.69 mM; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)|* "≥" means soluble, but saturation unknown.
溶解方案(动物实验)
"方案 一": "请依序添加每种溶剂:10% DMSO 40% PEG300 5% Tween-80 45% SalineSolubility: ≥ 2.5 mg/mL (3.81 mM); 澄清溶液 此方案可获得 ≥ 2.5 mg/mL(饱和度未知)的澄清溶液。以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;再向上述体系中加入 50 μL Tween-80,混合均匀;然后再继续加入 450 μL 生理盐水 定容至 1 mL。生理盐水的配制:将 0.9 g 氯化钠,溶解于 ddH₂O 并定容至 100 mL,可以得到澄清透明的生理盐水溶液。"
"方案 二": "请依序添加每种溶剂:10% DMSO 90% Corn OilSolubility: ≥ 2.5 mg/mL (3.81 mM); 澄清溶液 此方案可获得 ≥ 2.5 mg/mL(饱和度未知)的澄清溶液,此方案实验周期在半个月以上的动物实验酌情使用。以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。"
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文献和实验Richter A, Strausfeld U, et al. Effects of VM26 (teniposide), a specific inhibitor of type II DNA topoisomerase, on SV40 DNA replication in vivo. Nucleic Acids Res. 1987 Apr 24;15(8):3455-68.
Joyce H Lee, James M Berger. Cell Cycle-Dependent Control and Roles of DNA Topoisomerase II. Genes (Basel). 2019 Oct 30;10(11):859.
Li J, et al. Topoisomerase II trapping agent teniposide induces apoptosis and G2/M or S phase arrest of oral squamous cell carcinoma. World J Surg Oncol. 2006 Jul 6;4:41.
Attia SM, et al. Molecular cytogenetic evaluation of the aneugenic effects of teniposide in somatic and germinal cells of male mice. Mutagenesis. 2012 Jan;27(1):31-9.
Sun YC, et al. MiR-181b sensitizes glioma cells to teniposide by targeting MDM2. BMC Cancer. 2014 Aug 25;14:611.
The Role of Biotechnology in the Production of the Anticancer Compound Podophyllotox
Podophyllotoxin is a plant-derived compound found in Podophyllum sp. that is used to produce semi-synthetic anticancer pharmaceuticals such as etoposide, teniposide, and etoposide phosphate. This chapter describes the role
] teniposide|表鬼臼毒噻吩糖苷 tensin|张力蛋白[可维持微丝锚着点的张力] tenuin|细丝蛋白,细棒蛋白[一种肌肉蛋白] tenuivirus|细病毒组[一组植物病毒,模式成员是水稻条叶枯病毒] teratocarcinoma|畸胎癌[恶性的畸胎癌] teratogen|致畸剂 teratoma|畸胎瘤[由来自内胚层,中胚层和外胚层的混合组织组成的良性
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