5-Fluorouracil
5-Fluorouracil (5-FU) is an analogue of uracil and a potent antitumor agent. 5-Fluorouracil affects pyrimidine synthesis by inhibiting thymidylate synthetase thus depleting intracellular dTTP pools. 5-Fluorouracil induces apoptosis and can be used as a chemical sensitizer[1][2]. 5-Fluorouracil also inhibits HIV[3].
Product Specifications
CAS Number
[51-21-8]
Product Name Alternative
5-FU
UNSPSC
12352005
Hazard Statement
H301, H351
Target
Apoptosis; Endogenous Metabolite; HIV; Nucleoside Antimetabolite/Analog
Type
Reference compound
Related Pathways
Anti-infection; Apoptosis; Cell Cycle/DNA Damage; Metabolic Enzyme/Protease
Applications
Cancer-programmed cell death
Field of Research
Cancer
Assay Protocol
https://www.medchemexpress.com/5-Fluorouracil.html
Purity
99.99
Solubility
1 M Ammonium hydroxide : 50 mg/mL (ultrasonic) |DMSO : 50 mg/mL (ultrasonic) |H2O : 10 mg/mL (ultrasonic; warming; heat to 60°C)
Smiles
O=C(N1)NC=C(F)C1=O
Molecular Formula
C4H3FN2O2
Molecular Weight
130.08
Precautions
H301, H351
References & Citations
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, protect from light)
Scientific Category
Reference compound1
Clinical Information
Launched
Isoform
HIV
Available Sizes
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