Fludarabine
CAS No. 21679-14-1
Fludarabine ( F-ara-A | NSC 118218 )
产品货号. M13461 CAS No. 21679-14-1
Fludarabine(NSC 118218),一种 DNA 合成抑制剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥377 | 有现货 |
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| 10MG | ¥588 | 有现货 |
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| 25MG | ¥1088 | 有现货 |
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| 50MG | ¥1758 | 有现货 |
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| 100MG | ¥2385 | 有现货 |
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| 200MG | ¥3465 | 有现货 |
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| 500MG | ¥5517 | 有现货 |
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| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥378 | 有现货 |
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生物学信息
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产品名称Fludarabine
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Fludarabine(NSC 118218),一种 DNA 合成抑制剂。
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产品描述Fludarabine(NSC 118218), a DNA synthesis inhibitor, is a chemotherapy drug used in the treatment of hematological malignancies.(In Vitro):Fludarabine (5 μM; 48?hours) induces a decrease in p27kip1 expression.(In Vivo):Fludarabine (0.8?mg/kg; i.p.; two cycles for 5 days every 2 weeks) in combination with Cyclophosphamide (400?mg/kg; i.p.; 2 weeks) decreases incidence of GVHD.
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体外实验Fludarabine (5 μM; 48?hours) induces a decrease in p27kip1 expression.Western Blot Analysis Cell Line:B-CLL cells Concentration:5 μM Incubation Time:24 hours Result:Induces a decrease in p27kip1 expression. The decrease in p27kip1 expression was significantly correlated to the extent of in vitro apoptosis.
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体内实验Fludarabine (0.8?mg/kg; i.p.; two cycles for 5 days every 2 weeks) in combination with Cyclophosphamide (400?mg/kg; i.p.; 2 weeks) decreases incidence of GVHD. Animal Model:F-1 mice received 105 BCL-1 leukemia cells Dosage:0.8?mg/kg Administration:Intraperitoneal injection; two cycles for 5 days every 2 weeks Result:Combination with Cyclophosphamide decreased incidence of graft-versus-host disease (GVHD).
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同义词F-ara-A | NSC 118218
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通路JAK/STAT Signaling
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靶点STAT
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受体STAT1
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研究领域Cancer
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适应症——
化学信息
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CAS Number21679-14-1
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分子量285.23
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分子式C10H12FN5O4
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纯度>98% (HPLC)
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溶解度DMSO: 57 mg/mL (199.83 mM)
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SMILESNC1=C2N=CN([C@H]3[C@H]([C@@H]([C@@H](CO)O3)O)O)C2=NC(F)=N1
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化学全称(2R,3S,4S,5R)-2-(6-amino-2-fluoro-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Fernández-Calotti P, et al. Int Immunopharmacol. 2006, 6(5), 715-72
产品手册
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