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BIBR 1532

    
99%

BIBR 1532

源葉(MedMol)
S80637 一鍵復制產(chǎn)品信息
321674-73-1
C21H17NO3
331.36
2-[[(2E)-3-(2-萘基)-1-氧代-2-丁烯基]氨基]苯甲酸
貨號 規(guī)格 價格 上海 北京 武漢 南京 購買數(shù)量
S80637-5mg 99% ¥320.00 9 - - -
S80637-10mg 99% ¥560.00 8 - - -
S80637-50mg 99% ¥1900.00 2 - - -
產(chǎn)品介紹 參考文獻 質(zhì)檢證書(COA) 摩爾濃度計算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

BIBR 1532 is a potent, selective and non-competitive telomerase inhibitor with IC50 of 100 nM in a cell-free assay.

產(chǎn)品描述: BIBR 1532 is a potent, selective and non-competitive telomerase inhibitor with IC50 of 100 nM in a cell-free assay.
靶點: IC50: 100 nM (telomerase);Apoptosis;Telomerase
參考文獻: 1. Pascolo E, et al. Mechanism of human telomerase inhibition by BIBR1532, a synthetic, non-nucleosidic drug candidate. J Biol Chem. 2002 May 3;277(18):15566-72. 2. El-Daly H, et al. Selective cytotoxicity and telomere damage in leukemia cells using the telomerase inhibitor BIBR1532. Blood. 2005 Feb 15;105(4):1742-9. 3. Ward RJ, et al. Pharmacological telomerase inhibition can sensitize drug-resistant and drug-sensitive cells to chemotherapeutic treatment. Mol Pharmacol. 2005 Sep;68(3):779-86. 4. A R?th, et al. Short telomeres and high telomerase activity in T-cell prolymphocytic leukemia. Leukemia. 2007 Dec;21(12):2456-62. 5. Meng E, et al. Targeted inhibition of telomerase activity combined with chemotherapy demonstrates synergy in eliminating ovarian cancer spheroid-forming cells. Gynecol Oncol. 2012 Mar;124(3):598-605.
溶解性: DMSO  :  ≥  100  mg/mL  (301.79  mM)
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 3.018 ml 15.089 ml 30.179 ml
5 mM 0.604 ml 3.018 ml 6.036 ml
10 mM 0.302 ml 1.509 ml 3.018 ml
50 mM 0.06 ml 0.302 ml 0.604 ml
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參考文獻

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

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