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Ixabepilone

    
95.1%

Ixabepilone

源葉(MedMol)
S81436 一鍵復(fù)制產(chǎn)品信息
219989-84-1
C2H42N2O5S
506.7
伊沙匹隆;Ixempra; [1S-[1R*,3R*(E),7R*,10S*,11R*,12R*,16S*]]-7,11-dihydroxy-8,8,10,12,16-pentamethyl-3-[1-methyl-2-(2-methyl-4-thiazolyl)ethenyl]-4-aza-17-oxabicyclo[14.1.0]heptadecane-5,9-dione; 16-aza-ep
貨號 規(guī)格 價格 上海 北京 武漢 南京 購買數(shù)量
S81436-1mg
95.1% ¥326.40 5 - - -
S81436-2mg
95.1% ¥544.00 5 - - -
S81436-5mg
95.1% ¥1020.00 4 - - -
S81436-10mg
95.1% ¥1496.00 5 - - -
S81436-25mg
≥95% ¥3060.00 貨期:2-3天 - - -
S81436-50mg
≥95% ¥4800.00 貨期:2-3天 - - -
產(chǎn)品介紹 參考文獻(xiàn) 質(zhì)檢證書(COA) 摩爾濃度計算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

Ixabepilone (BMS-247550) is an orally bioavailable microtubule inhibitor, which binds to tubulin and promotes tubulin polymerization and microtubule stabilization, thereby arrests cells in the G2-M phase of the cell cycle and induces tumor cell apoptosis.

產(chǎn)品描述: Ixabepilone (BMS-247550) is an orally bioavailable microtubule inhibitor, which binds to tubulin and promotes tubulin polymerization and microtubule stabilization, thereby arrests cells in the G2-M phase of the cell cycle and induces tumor cell apoptosis.
靶點: Apoptosis;Microtubule Associated;Apoptosis;?MicrotubuleAssociated
體內(nèi)研究: In vivo, BMS-247550 has clearly demonstrated antitumor activity that is superior to paclitaxel in both paclitaxel-resistant and -sensitive tumors. BMS-247550 is more efficacious compared to paclitaxel in all five paclitaxel-resistant tumors evaluated in this study (four human and one murine): i.e., the clinically derived paclitaxel resistant Pat-7 ovarian carcinoma, the A2780Tax ovarian carcinoma that is resistant to paclitaxel because of tubulin mutations, the HCT116/VM46 MDR colon carcinoma, the clinically derived paclitaxel-resistant Pat-21 breast carcinoma, and the murine fibrosarcoma M5076. Against three paclitaxel-sensitive human tumor xenografts, BMS-247550 produces antitumor activity equivalent to paclitaxel: i.e., A2780 human ovarian carcinoma, HCT116, and LS174T human colon carcinoma
細(xì)胞實驗: HCT116 cells from cultures are collected by trypsinization after 1, 2, 4, 8, 16, and 24 h exposure to 7.5 nm of BMS-247550. Cells are pelleted and fixed in 80% ethanol at ?20°C. After an overnight storage at ?20°C, cells are rehydrated with PBS buffer and DNA stain by incubation with propidium iodide (5 μg/ml) in 0.1% RNase for 15–30 min. Fluorescence-activated cell sorter acquisition is performed using the FACS Calibur instrument and analysis is done using Cellquest and Modfit software. (Only for Reference)
參考文獻(xiàn): 1.Lee FY, et al. Clin Cancer Res. 2001, 7(5):1429-1437.
溶解性: Ethanol:93  mg/mL  (183.5  mM)    DMSO:93  mg/mL  (183.5  mM)    H2O:<1  mg/mL
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 1.974 ml 9.868 ml 19.736 ml
5 mM 0.395 ml 1.974 ml 3.947 ml
10 mM 0.197 ml 0.987 ml 1.974 ml
50 mM 0.039 ml 0.197 ml 0.395 ml
注意: 部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權(quán)威性,僅供客戶參考交流研究之用。

參考文獻(xiàn)

質(zhì)檢證書(COA)

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批號:JS298415 貨號:S20001-25g
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摩爾濃度計算器

質(zhì)量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)

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