CARMOFUR

Carmofur is a 5FU derivative inhibiting DNA synthesis, used in oncology. Side effects include GI upset, myelosuppression, and skin reactions. Only GMP materials will be supplied, logistics all according to GDP.

SKU: 62781333321b Category: Tag:

Product Description


Mechanism of action

Carmofur is a lipophilic fluoropyrimidine derivative and prodrug of 5fluorouracil (5FU). It inhibits thymidylate synthase, depleting dTMP required for DNA synthesis, and incorporates into RNA to disrupt transcription. Carmofur also inhibits acid ceramidase, accumulating ceramide and inducing apoptosis through sphingolipidmediated pathways.

Benefits and advantages

Used in anticancer research, fluoropyrimidinepathway studies, thymidylatesynthase inhibition assays, sphingolipidsignalling research, apoptosis modelling, colorectalcancer studies and chemoresistance analysis.

Side effects and risks

Risks include myelosuppression, diarrhoea, mucositis, hepatotoxicity, neurotoxicity and dermatologic reactions. Handle with cytotoxiccompound containment.

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

Datasheet


Molecular Formula

C11H15FN2O3

Molecular Weight

257.26 g/mol

CAS Number

61422-45-5

Storage Condition

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

Solubility

Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance.

Purity

Purity information is available upon request (COA).

Synonym

carmofur; 61422-45-5; Mifurol; HCFU; 1-Hexylcarbamoyl-5-fluorouracil

IUPAC/Chemical Name

5-fluoro-N-hexyl-2,4-dioxopyrimidine-1-carboxamide

InChl Key

AOCCBINRVIKJHY-UHFFFAOYSA-N

InChl Code

InChI=1S/C11H16FN3O3/c1-2-3-4-5-6-13-10(17)15-7-8(12)9(16)14-11(15)18/h7H,2-6H2,1H3,(H,13,17)(H,14,16,18)

References

https://pubchem.ncbi.nlm.nih.gov/compound/2577;

3D Conformer.

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