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Fludarabine Phosphate

SKU: orb1300713

Description

Fludarabine Phosphate is a fluorinated antimetabolite derived from vidarabine. Upon intracellular conversion to its active triphosphate form, it inhibits DNA synthesis enzymes like DNA polymerase alpha, disrupting tumor cell proliferation. It is widely used in research, including in vitro and in vivo studies, for investigating hematological cancers and chemotherapy mechanisms.

Research Area

Cell Biology, Molecular Biology

Images & Validation

Key Properties

CAS Number75607-67-9
MW365.21
Purity99.78%
FormulaC10H13FN5O7P
SMILESNc1nc(F)nc2n(cnc12)[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@@H]1O
TargetDNA/RNA Synthesis,Nucleoside Antimetabolite/Analog,Apoptosis
Solubility10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (5.48 mM);DMSO:35 mg/mL (95.84 mM);Ethanol:< 1 mg/mL (insoluble or slightly soluble);H2O:2 mg/mL (5.48 mM)

Bioactivity

Target IC50
DNA polymerase δ:1.3 μM(Ki)|DNA polymerase α:1.1 μM(Ki )
In Vivo
Fludarabine Phosphate effectively inhibits DNA polymerase α/δ (Ki: 1.1/1.3 μM), demonstrating potent inhibitory activity in vitro It is capable of being excised from bound DNA by DNA polymerase δ. Competitively binding with deoxyadenosine triphosphate a the A site for DNA chain elongation, Fludarabine Phosphate leads to the termination of DNA st and extension. Notably, human DNA polymerase α is more adept at incorporating Fludarabine Phosphate into DNA than polymerase δ.
In Vitro
The maximum tolerable dose of Fludarabine Phosphate is determined to be 234 mg/kg, with its LD50 (lethal dose 50%) for mice being 375 mg/kg. Notably, Fludarabine Phosphate exhibits toxicity in tumor-free mice. however, in mice carrying P388 leukemia, treatment with Fludarabine Phosphate leads to a reduction in the number of surviving cells geared towards therapy, significantly enhancin the lifespan by 110% and increasin the average survival time.
Cell Research
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 o the drugs is expressed as a percentage of survival relative to that of untreated control cells.(Only for Reference)

Storage & Handling

StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

DNA polymerase α, DNA polymerase δ, DNA Synthesis, DNASynthesis, Analog, Apoptosis, Inhibitor, NSC118218, NSC-118218, NSC 118218, NSC 312887 Phosphate, inhibit, Nucleoside Antimetabolite, Nucleoside Antimetabolite/Analog, NucleosideAntimetabolite, NSC312887 Phosphate, NSC-312887 Phosphate, F-ara-A (NSC 312887) Phosphate, F-ara-AMP, fludara Phosphate, Fludarabine, Fludarabine Phosphate, RNA Synthesis, RNASynthesis

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  • Fludarabine Phosphate [orb1224062]

    >98%(HPLC)

    75607-67-9

    365.2

    C10H13FN5O7P

    1 g, 500 mg, 50 mg, 10 mg, 25 mg, 100 mg, 200 mg, 5 mg
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Key Properties

No computed properties available.

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Fludarabine Phosphate (orb1300713)

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

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5 mg
¥ 1,040.00
1 ml x 10 mM (in DMSO)
¥ 1,170.00
10 mg
¥ 1,300.00
25 mg
¥ 1,690.00
50 mg
¥ 2,080.00
100 mg
¥ 2,470.00
200 mg
¥ 3,250.00
500 mg
¥ 4,940.00
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