About MedicaPharma
MedicaPharma distributes high-quality active pharmaceutical ingredients (APIs) to hospitals, commercial (compounding) pharmacies, research institutes, and universities worldwide.
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Let us handle your sourcing / supply activities. Highly experienced in sourcing specialty raw pharmaceutical ingredients from niche GMP manufacturers around the world.
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Niche API specialist - Pro-active supply partner - High service level - Global network - Logistics according to GDP regulations
Product Description
Mechanism of Action
Fluorocytosine (5‑FC) is converted by fungal cytosine deaminase to 5‑FU, disrupting RNA and DNA synthesis in susceptible fungi.
Benefits and Advantages
Used in antifungal synergy research, nucleic‑acid pathway analysis and fungal metabolism modelling.
Side Effects and Risks
Bone‑marrow suppression, GI toxicity and hepatotoxicity.
Datasheet
| Molecular Formula | C4H4FN3O |
|---|---|
| Molecular Weight | 129.09 g/mol |
| CAS Number | 2022-85-7 |
| Storage Condition | Keep container tightly closed in a dry and well-ventilated place. Light sensitive. Keep in a dry place. |
| 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 | 5-Fluorocytosine; flucytosine; 2022-85-7; Fluorocytosine; Ancobon |
| IUPAC/Chemical Name | 6-amino-5-fluoro-1H-pyrimidin-2-one |
| InChl Key | XRECTZIEBJDKEO-UHFFFAOYSA-N |
| InChl Code | InChI=1S/C4H4FN3O/c5-2-1-7-4(9)8-3(2)6/h1H,(H3,6,7,8,9) |
| References |
3D Conformer.
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