Fludarabine Phosphate

製品コードS1229 バッチS122904

印刷

化学情報

Chemical Structure Synonyms F-ara-A Phosphate, NSC 118218 Phosphate Storage
(From the date of receipt)		 3 years -20°C powder
1 years -80°C in solvent
化学式

C10H13FN5O7P
分子量 365.21 CAS No. 75607-67-9
Solubility (25°C)* 体外 DMSO 73 mg/mL (199.88 mM)
Water (warmed with 50ºC water bath) 6 mg/mL (16.42 mM)
Ethanol Insoluble
体内 （毎回新しく調製した物を用意してください）
Homogeneous suspension
CMC-NA
≥5mg/ml Taking the 1 mL working solution as an example, add 5 mg of this product to 1 ml of CMC-Na solution, mix evenly to obtain a homogeneous suspension with a final concentration of 5 mg/ml.
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

溶剤液（一定の濃度）を調合する

生物活性

製品説明 Fludarabine Phosphate is an analogue of adenosine and deoxyadenosine, which is able to compete with dATP for incorporation into DNA and inhibit DNA synthesis.
in vitro Fludarabine Phosphate is converted to F-ara-ATP in cells and then incorporated into DNA in a self-limiting manner. This compound competes with dATP for incorporation into the A site of the extending DNA strand, which results in termination of DNA strand elongation. Human DNA polymerase α incorporates more of this chemical into DNA than polymerase δ. It completively inhibits DNA polymerase α and DNA polymerase δ with Ki of 1.1 μM and 1.3 μM, respectively. DNA polymerase δ is also able to excise the incorporated Fludarabine Phosphate from DNA in vitro. [1]
in vivo Fludarabine Phosphate is toxic for tumor-free mice. The maximum tolerated dose (LD10) of this compound administered as a single dose is 234 mg/kg. The 50% lethal dose is 375 mg/kg. This chemical administered as a single dose induces fewer number of cells surviving therapy in mice bearing P388 leukemia, accompanied by greater percentage of increase in life span (110%) and increased median survival time. [3]

プロトコル(参考用のみ)

細胞アッセイ 細胞株 Human T lymphoblastoid cells
濃度 30 μM
反応時間 5 hours
実験の流れ Cells are incubated with Fludarabine Phosphate for 5 hr and washed twice with drug-free warm medium. 800 cells are mixed with 1.3 mL of 0.25% soft agar in Dulbecco’s medium supplemented with 20% fetal bovine serum (pre-warmed to 37 ℃) and incubated in a tissue culture dish for 10 days (humidified 5% CO2 , 37 ℃). At the end of the incubation period, colonies of more than 40 cells are scored under a microscope. The cytotoxic effect of this compound is expressed as a percentage of survival relative to that of untreated control cells.
動物実験 動物モデル Murine Leukemia P3881
投薬量 234 mg/kg
投与方法 A single dose i.p. at day 1

参考

  • https://pubmed.ncbi.nlm.nih.gov/1697861/
  • https://pubmed.ncbi.nlm.nih.gov/6210262/
  • https://pubmed.ncbi.nlm.nih.gov/7083151/

カスタマーフィードバック

Data from [Data independently produced by Mol Cancer Ther, 2014, 13(10), 2276-87]

Selleckの高級品が、幾つかの出版された研究調査結果（以下を含む）で使われた：

PDK4-driven lactate accumulation facilitates LPCAT2 lactylation to exacerbate sepsis-induced acute lung injury [ Cell Death Differ, 2025, 10.1038/s41418-025-01585-6] PubMed: 41057687
Effect of opioid receptor antagonist on mitigating tumor necrosis factor-like weak inducer of apoptosis (TWEAK)-induced apoptolysis in pemphigus pathogenesis [ J Autoimmun, 2024, 149:103307] PubMed: 39276627
Disrupting pro-survival and inflammatory pathways with dimethyl fumarate sensitizes chronic lymphocytic leukemia to cell death [ Cell Death Dis, 2024, 15(3):224] PubMed: 38494482
A chemical probe inhibitor targeting STAT1 restricts cancer stem cell traits and angiogenesis in colorectal cancer [ J Biomed Sci, 2022, 29(1):20] PubMed: 35313878
Z-DNA binding protein 1 mediates necroptotic and apoptotic cell death pathways in murine astrocytes following herpes simplex virus-1 infection [ J Neuroinflammation, 2022, 19(1):109] PubMed: 35549723
MMP-10 from M1 macrophages promotes pulmonary vascular remodeling and pulmonary arterial hypertension [ Int J Biol Sci, 2022, 18(1):331-348] PubMed: 34975336
A Drug Repurposing Screen Identifies Fludarabine Phosphate as a Potential Therapeutic Agent for N-MYC Overexpressing Neuroendocrine Prostate Cancers [ Cells, 2022, 11-142246] PubMed: 35883689
A Drug Repurposing Screen Identifies Fludarabine Phosphate as a Potential Therapeutic Agent for N-MYC Overexpressing Neuroendocrine Prostate Cancers [ Cells, 2022, 11-142246] PubMed: 35883689
RNase 7 Inhibits Uropathogenic Escherichia coli-Induced Inflammation in Bladder Cells under a High-Glucose Environment by Regulating the JAK/STAT Signaling Pathway [ Int J Mol Sci, 2022, 23(9)5156] PubMed: 35563546
ABT199/venetoclax potentiates the cytotoxicity of alkylating agents and fludarabine in acute myeloid leukemia cells [ Oncotarget, 2022, 13:319-330] PubMed: 35154579

長期の保管のために-20°Cの下で製品を保ってください。

人間や獣医の診断であるか治療的な使用のためにでない。

各々の製品のための特定の保管と取扱い情報は、製品データシートの上で示されます。大部分のSelleck製品は、推薦された状況の下で安定です。製品は、推薦された保管温度と異なる温度で、時々出荷されます。長期の保管のために必要とされてそれと異なる温度で、多くの製品は、短期もので安定です。品質を維持するが、夜通しの積荷のために最も経済的な貯蔵状況を用いてあなたの送料を保存する状況の下に、製品が出荷されることを、我々は確実とします。製品の受領と同時に、製品データシートの上で貯蔵推薦に従ってください。