DOXIFLURIDINE

Doxifluridine is an oral prodrug of 5FU that inhibits DNA synthesis in cancer cells. Side effects include myelosuppression, mucositis, and GI discomfort. Only GMP materials will be supplied, logistics all according to GDP.

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Product Description


Mechanism of Action

Doxifluridine is an oral prodrug of 5fluorouracil (5FU). It undergoes conversion by pyrimidine phosphorylase, which is highly expressed in tumour tissue, generating cytotoxic 5FU locally. 5FU inhibits thymidylate synthase and incorporates into RNA and DNA, disrupting replication and transcription.

Benefits and Advantages

Used in tumourtargeted prodrug research, pyrimidinepathway studies, 5FU activation assays, oncologymodel development and nucleotideantimetabolite mechanism analysis.

Side Effects and Risks

Risks include myelosuppression, mucositis, GI toxicity, cardiotoxicity (rare) and dermatologic reactions. Handle with cytotoxicantimetabolite precautions.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C9H11FN2O5

Molecular Weight

246.19 g/mol

CAS Number

436349

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

>36.9 [ug/mL] (The mean of the results at pH 7.4)

Purity

Purity information is available upon request (COA).

Synonym

doxifluridine; 5'-Deoxy-5-fluorouridine; 5-fluoro-5'-deoxyuridine; Furtulon; 3094-09-5

IUPAC/Chemical Name

1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-methyloxolan-2-yl]-5-fluoropyrimidine-2,4-dione

InChl Key

ZWAOHEXOSAUJHY-ZIYNGMLESA-N

InChl Code

InChI=1S/C9H11FN2O5/c1-3-5(13)6(14)8(17-3)12-2-4(10)7(15)11-9(12)16/h2-3,5-6,8,13-14H,1H3,(H,11,15,16)/t3-,5-,6-,8-/m1/s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/18343;

3D Conformer.

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