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BioChemicals
Fludarabine
tcsc2133
Fludarabine
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AVAILABLE SIZES
5mg
10mg
50mg
$
86.00
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ORDERING INFORMATION
International
TAICLONE BIOTECH CORP.
order@taiclone.com
+886-2-2735-9682
+886-2-2735-9807
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Product Description
Fludarabine(NSC 118218), a DNA synthesis inhibitor, is a chemotherapy drug used in the treatment of hematological malignancies.
Target:
Fludarabine or fludarabine ph osphate (Fludara) is a chemotherapy drug used in the treatment of hematological malignancies (cancers of blood cells such as leukemias and lymphomas). It is a purine analog, which interferes with DNA synthesis. Fludarabine is highly effective in the treatment of chronic lymphocytic leukemia, producing higher response rates than alkylating agents such as chlorambucil alone.
Fludarabine is a purine analog, and can be given both orally and intravenously. Fludarabine inhibits DNA synthesis by interfering with ribonucleotide reductase and DNA polymerase. It is active against both dividing and resting cells. Being phosphorylated, fludarabine is ionized at physiologic pH and is effectually trapped in blood. This provides some level of specificity for blood cells, both cancerous and healthy. Fludarabine is associated with the development of severe autoimmune hemolytic anemia in a proportion of patients. Difficulties are often encountered when harvesting peripheral blood stem cells from patients previously treated with fludarabine.
Information
CAS No
21679-14-1
Formula
C
10
H
12
FN
5
O
4
Clinical Information
clinicalinformation
Pathway
Cell Cycle/DNA Damage
Target
Nucleoside Antimetabolite/Analog
Specifications
Purity / Grade
>98%
Solubility
DMSO : ≥ 160 mg/mL (560.95 mM)
Smiles
smiles
Misc Information
Alternative Names
F-ara-A;NSC 118218
Observed Molecular Weight
285.23
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