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Epothilone B

Epothilone B

产品编号 T6075   CAS 152044-54-7
别名: 帕妥匹隆, Patupilone, EPO 906

Epothilone B (EPO 906) 是微管稳定剂,Ki 为0.71 μM。 它与αβ-微管蛋白异二聚体亚基结合,使αβ-微管蛋白解离减少。

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Epothilone B Chemical Structure
Epothilone B, CAS 152044-54-7
规格 价格/CNY 货期 数量
1 mg ¥ 289 现货
2 mg ¥ 413 现货
5 mg ¥ 578 现货
10 mg ¥ 996 现货
25 mg ¥ 1,660 现货
50 mg ¥ 2,470 现货
100 mg ¥ 3,680 现货
1 mL * 10 mM (in DMSO) ¥ 648 现货
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
重组蛋白限时优惠
Doxorubicin hydrochloride限时半价
产品目录号及名称: Epothilone B (T6075)
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纯度: 99.54%
纯度: 99.48%
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生物活性
化学信息
存储 & 溶解度
参考文献
产品描述 Epothilone B (EPO 906) is a compound isolated from the myxobacterium Sorangium cellulosum. Similar to paclitaxel, patupilone induces microtubule polymerization and stabilizes microtubules against depolymerization conditions. In addition to promoting tubulin polymerization and stabilization of microtubules, this agent is cytotoxic for cells overexpressing P-glycoprotein, a characteristic that distinguishes it from the taxanes. Patupilone may cause complete cell-cycle arrest.
靶点活性 Tubulin:1.8 μM(EC0.01)
体外活性 Epothilone B shows better activity than Epothilone A. The EC0.01 of Epothilone B is 1.8 μM. Epothilone B potently inhibits cell proliferation in HCT116 cells, with IC50 of 0.8 nM. [1] Epothilone B induces mitotic arrest and displays cytotoxicity in KB3-1, KBV-1, Hela, and Hs578T cells, with IC50 of 3 nM to 92 nM. Epothilone B competes with Taxol in binding to microtubules, with IC50 of 3.3 μM. [2] In MCF-7 cells overexpressing GFP-α-tubulin, Epothilone B (3.5 nM) efficiently blocks microtubule dynamics. Meanwhile, Epothilone B induces mitotic arrest with IC50 of 3.5 nM. [3] In multiple myeloma (MM) cells, including RPMI 8226, U266, MM.1S, LR5, and MR20, Epothilone B directly suppresses proliferation with IC50 of 1 nM to 10 nM. Similarly, Epothilone B (10 nM) also induces cell cycle arrest and apoptosis. [4] A recent study reveals that, in ovarian cancer Hey cells, Epothilone B (5 nM–100 nM) enhances surface epithelial cell adhesion antigen (EpCAM), without affecting the transcription or the total cellular level of EpCAM. [5]
体内活性 In a mouse xenograft model of RPMI 8226 cells, Epothilone B (2.5 mg/kg–4 mg/kg) prolongs survival and suppresses tumor growth. [4] Similarly, in mouse xenograft models of prostate cancer cells, including DU145 and PC3, Epothilone B at the same dose also inhibits tumor growth. [6]
激酶实验 Tubulin polymerization assay: Calf brain microtubule proteins (MTP) are purified, which includes approximately 15%–20% microtubule associated proteins. The buffer (MES buffer) used for the Epothilone B-microtubule studies contains 0.1 M 2-morpholinoethanesulfonic acid (MES), 1 mM EGTA, 0.5 mM MgCl2, and 3 M glycerol at pH 6.6. Samples for electron microscopy are placed on carbon-over-Parlodion-coated grids (300 mesh) and negatively stained with 2% uranyl acetate. Microtubule assembly in the presence or absence of Epothilone B is monitored spectrophotometrically by using a spectrophotometer equipped with a thermostatically regulated liquid circulator. The temperature is held at 35 °C and changes in turbidity (representative of polymer mass) are monitored at 350 nm. Effective concentration (EC0.01), defined as the interpolated concentration capable of inducing an initial slope of 0.01 OD/min rate, is calculated using the formula EC0.01 = concentration/slope and expressed as the mean with standard deviation obtained from three different concentrations.
细胞实验 For mitotic block and aberrant mitosis, cells are plated either in 48-well plates (for trypan blue and cell counting) or onto coverslips. After 24 hours, cells are treated with Epothilone B and scored at regular intervals. For the cytotoxicity analysis, cells are counted and scored as trypan blue positive or negative. Concurrently, coverslips andaliquots of cells in the culture supernatant are fixed and stained with Hoechst33342 in PBS. These cells are scored for cells blocked at the G2/M transition and aberrant mitosis.(Only for Reference)
别名 帕妥匹隆, Patupilone, EPO 906
分子量 507.68
分子式 C27H41NO6S
CAS No. 152044-54-7

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

DMSO: 5.1 mg/mL (10 mM)

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 1.9697 mL 9.8487 mL 19.6974 mL 49.2436 mL
5 mM 0.3939 mL 1.9697 mL 3.9395 mL 9.8487 mL
10 mM 0.197 mL 0.9849 mL 1.9697 mL 4.9244 mL

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TargetMol Library Books参考文献

1. Regueiro-Ren A , et al. Org Lett, 2001, 3(17), 2693-2696. 2. Bollag DM, et al. Cancer Res, 1995, 55(11), 2325-2333. 3. Kamath K, et al. Cancer Res, 2003, 63(18), 6026-6031. 4. Lin B, et al. Blood, 2005, 105(1), 350-357. 5. Shahabi S, et al. Gynecol Oncol, 2010, 119(2), 345-350.
Cysteamine hydrochloride 5-LOX-IN-2 Tebufenozide Brevilin A Indirubin Piclidenoson Tuvusertib WYE-132

相关化合物库

该产品包含在如下化合物库中:
抗癌临床化合物库 药物功能重定位化合物库 抗癌药物库 抗癌活性化合物库 微管靶向化合物库 抗衰老化合物库 抗感染化合物库 细胞骨架化合物库 共价抑制剂库 抗生素库

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体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。

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您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。

Keywords

Epothilone B 152044-54-7 Apoptosis Cytoskeletal Signaling Microbiology/Virology Microtubule Associated Antibiotic Antifungal EPO-906 帕妥匹隆 Microtubule/Tubulin Inhibitor Patupilone inhibit EPO 906 Fungal EPO906 inhibitor

 

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