天然产物 糖类和糖苷 Saccharides and Glycosides
10-Deacetyl-7-xylosyl paclitaxel;(Synonyms: 10-Deacetyl-7-xylosyltaxol; 10-Deacetylpaclitaxel 7-Xyloside; 10-Deacetyltaxol 7-Xyloside) 纯度: 98.19%
10-Deacetyl-7-xylosyl paclitaxel 是 Paclitaxel (一种 microtubule 稳定剂,增强 tubulin 聚合) 的衍生物,相比 Paclitaxel,具有更好的药学活性。
10-Deacetyl-7-xylosyl paclitaxel Chemical Structure
CAS No. : 90332-63-1
规格 | 价格 | 是否有货 | 数量 |
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10 mg | ¥800 | In-stock | |
50 mg | ¥2650 | 询价 | |
100 mg | ; | 询价 | ; |
200 mg | ; | 询价 | ; |
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10-Deacetyl-7-xylosyl paclitaxel 相关产品
bull;相关化合物库:
- Natural Product Library Plus
- Bioactive Compound Library Plus
- Toxins for Antibody-Drug Conjugate Research Library
生物活性 |
10-Deacetyl-7-xylosyl paclitaxel is a Paclitaxel (a microtubule stabilizing agent; enhances tubulin polymerization) derivative with improved pharmacological features. IC50 value: Target: Microtubule inhibitor 10-Deacetyl-7-xylosyl paclitaxel induced mitotic cell cycle arrest and apoptosis as measured by flow cytometry, DNA laddering, and transmission electron microscopy. Pro-apoptotic Bax and Bad protein expression was up-regulated and anti-apoptotic Bcl-2 and Bcl-XL expression down-regulated, which lead to a disturbance of the mitochondrial membrane permeability and to the activation of caspase-9. In turn, caspase-9 activated downstream caspases-3 and -6, but not caspase-8. Bid was also activated by caspase-3. Reversely, treatment with a caspase-10-specific inhibitor could not protect PC-3 cells from 7-xylosyl-10-deacetyl-paclitaxel-triggered apoptosis. Moreover, 7-xylosyl-10-deacetylpaclitaxel had no effect on the expression of CD95 and NF-kappaB proteins, indicating that apoptosis was induced through the mitochondrial-dependent pathway in PC-3 cells. |
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IC50 Target |
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分子量 |
943.98 |
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Formula |
C50H57NO17 |
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CAS 号 |
90332-63-1 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
4deg;C, protect from light *In solvent : -80deg;C, 6 months; -20deg;C, 1 month (protect from light) |
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溶解性数据 |
In Vitro:;
DMSO : 33.33 mg/mL (35.31 mM; Need ultrasonic) H2O : < 0.1 mg/mL (insoluble) 配制储备液
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
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参考文献 |
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