GLPBio

Fludarabine

Catalog No.: GC14144Purity:>98.00%Synonyms: 2-fluoro-ara-A, NSC 118218
Fludarabin (NSC 118218) ist ein Inhibitor der DNA-Synthese und ein fluoriertes Purin-Analogon mit antineoplastischer AktivitÄt bei malignen lymphoproliferativen Erkrankungen. Fludarabin hemmt die Zytokin-induzierte Aktivierung von STAT1 und die STAT1-abhÄngige Gentranskription in normalen ruhenden oder aktivierten Lymphozyten.

Die Produkte sind ausschließlich für Forschungszwecke bestimmt. Nicht zur Anwendung am Menschen. Wir verkaufen nicht an Patienten.


Fludarabine
Cas No.: 21679-14-1
10mM (in 1mL DMSO)In Stock
$38.00
1
1mgIn Stock
$22.00
1
5mgIn Stock
$34.00
1
10mgIn Stock
$52.00
1
25mgIn Stock
$100.00
1
50mgIn Stock
$160.00
1
100mgIn Stock
$224.00
1

Zitate (Citations)

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    Nature
    641, 529–536 (2025)
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    632, 686–694 (2024)
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    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    388(6745) (2025)
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    387(6734) (2025)
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    35, 97–116 (2025)
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    33, 904–922 (2023)
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    31, 1291–1307 (2021)

Beschreibung (Description)

Fludarabine is a purine analog that inhibits DNA synthesis[1]. Fludarabine inhibits cytokine-induced activation of STAT1 and STAT1-dependent gene transcription in normal quiescent or activated lymphocytes[2]. Fludarabine is an anti-tumor agent used to treat leukemia and lymphoma[3].

In vitro, treatment of MEC-2 cells with Fludarabine (100μM) for 72h significantly reduced cell viability, induced cytochrome c release and DNA cleavage[4]. Treatment of chronic lymphocytic leukemia (CLL) cells with Fludarabine (3, 10, 30μM) for 24-72h induced apoptosis in a dose- and time-dependent manner, increased intracellular phosphorylation of H2A histone family member X (H2AX), and led to DNA damage[5].

In vivo, treatment of BCL-1-bearing F1 mice with Fludarabine (0.8mg/kg) by intraperitoneal injection reduced the incidence of graft-versus-host disease (GVHD) in mice and maintained the anti-leukemic effect after leukemic cell transplantation[6]. Treatment of SCID beige mice with Fludarabine (200mg/kg) by intraperitoneal injection for 6 weeks promoted the engraftment of acute myeloid leukemia (AML) cell lines[7].

References:
[1] Wang Y, Chen X, Tang N, et al. Boosting Clear Cell Renal Carcinoma-Specific Drug Discovery Using a Deep Learning Algorithm and Single-Cell Analysis[J]. International Journal of Molecular Sciences, 2024, 25(7): 4134.
[2] Battle T E, Frank D A. STAT1 mediates differentiation of chronic lymphocytic leukemia cells in response to Bryostatin 1[J]. Blood, 2003, 102(8): 3016-3024.
[3] Ricci F, Tedeschi A, Morra E, et al. Fludarabine in the treatment of chronic lymphocytic leukemia: a review[J]. Therapeutics and clinical risk management, 2009: 187-207.
[4] Huang C, Tu Y, Freter C E. Fludarabine-resistance associates with ceramide metabolism and leukemia stem cell development in chronic lymphocytic leukemia[J]. Oncotarget, 2018, 9(69): 33124.
[5] El-Mabhouh A A, Ayres M L, Shpall E J, et al. Evaluation of bendamustine in combination with fludarabine in primary chronic lymphocytic leukemia cells[J]. Blood, The Journal of the American Society of Hematology, 2014, 123(24): 3780-3789.
[6] Weiss L, Abdul-Hai A, Or R, et al. Fludarabine in combination with cyclophosphamide decreases incidence of GVHD and maintains effective graft-versus-leukemia effect after allogeneic stem cell transplantation in murine lymphocytic leukemia[J]. Bone marrow transplantation, 2003, 31(1): 11-15.
[7]Pievani A, Michelozzi I M, Rambaldi B, et al. Fludarabine as a cost-effective adjuvant to enhance engraftment of human normal and malignant hematopoiesis in immunodeficient mice[J]. Scientific RepoRts, 2018, 8(1): 9125.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

MEC-2 cells、Flu-resistant clonal cells

Preparation Method

Cells were treated with or without 100µM Fludarabine for 72h and cell viability was analyzed by MTT. 

Reaction Conditions

100μM; 72h

Applications

Fludarabine induces MEC-2 cells apoptosis but not flu-resistant clonal cells.

Animal experiment [2]:

Animal models

B-cell leukemia (BCL-1) bearing (BALB/c×C57BL/6) F1 mice 

Preparation Method

Mice received 105 BCL-1 leukemic cells and 1 day later were given 0.8mg/kg Fludarabine intraperitoneally for 5 consecutive days. 2 weeks later, mice received another 5-day cycle of 0.8mg/kg Fludarabine and 2 weeks later received 400mg/kg cyclophosphamide intraperitoneally. Control animals received saline instead of fludarabine. One day after cyclophosphamide treatment, C57BL/6 precursor cells were transplanted and the development of leukemia and the extent of graft-versus-host disease (GVHD) were monitored clinically and histopathologically.

Dosage form

0.8mg/kg, two cycles for 5 days every 2 weeks; i.p.

Applications

Fludarabine in combination with cyclophosphamide decreases incidence of GVHD and maintains effective graft-versus-leukemia effect after allogeneic stem cell transplantation in murine lymphocytic leukemia.

References:
[1]Huang C, Tu Y, Freter C E. Fludarabine-resistance associates with ceramide metabolism and leukemia stem cell development in chronic lymphocytic leukemia[J]. Oncotarget, 2018, 9(69): 33124.
[2]Weiss L, Abdul-Hai A, Or R, et al. Fludarabine in combination with cyclophosphamide decreases incidence of GVHD and maintains effective graft-versus-leukemia effect after allogeneic stem cell transplantation in murine lymphocytic leukemia[J]. Bone marrow transplantation, 2003, 31(1): 11-15.

Produktdokumente (Product Documents)

Purity:>98.00%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
21679-14-1
Synonyme
2-fluoro-ara-A, NSC 118218
Chemischer Name
(2R,3S,4S,5R)-2-(6-amino-2-fluoropurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
SMILES
C1=NC2=C(N1C3C(C(C(O3)CO)O)O)N=C(N=C2N)F
Summenformel
C10H12FN5O4
Molekulargewicht
285.23
Löslichkeit
≥ 9.25mg/mL in DMSO
Lagerung
Store at -20°C
Allgemeine Hinweise
Wählen Sie anhand der Löslichkeitsdaten des Produkts ein geeignetes Lösungsmittel. Aliquotieren Sie die Stammlösung nach der Herstellung, um wiederholte Gefrier-Auftau-Zyklen zu vermeiden.
Verwenden Sie Stammlösungen bei Lagerung bei -80°C innerhalb von 6 Monaten bzw. bei -20°C innerhalb von 1 Monat.
Zur Verbesserung der Löslichkeit das Röhrchen auf 37°C erwärmen und für eine angemessene Dauer beschallen.
Versandbedingungen
Evaluierungsmuster werden mit Kühlakkus versandt. Andere verfügbare Größen werden bei Raumtemperatur oder auf Anfrage mit Kühlakkus versandt.

Rechner (Calculators)Molarität / Verdünnung / Molekulargewicht / Einheitenumrechnung / In-vivo-Formulierung / Löslichkeit

g/mol

Reviews

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