Cyclopentenyl uracil
Cyclopentenyl uracil, a non-cytotoxic inhibitor of uridine kinase, effectively blocks the salvage of circulating uridine by host and tumor tissues in the intact mouse[1].
Product Specifications
CAS Number
[90597-20-9]
UNSPSC
12352005
Target
UGT
Type
Reference compound
Related Pathways
Metabolic Enzyme/Protease
Applications
Cancer-Kinase/protease
Field of Research
Cancer
Assay Protocol
https://www.medchemexpress.com/cyclopentenyl-uracil.html
Purity
99.11
Solubility
DMSO : 100 mg/mL (ultrasonic)
Smiles
O[C@H]1[C@@](N2C(NC(C=C2)=O)=O)([H])C=C([C@H]1O)CO
Molecular Formula
C10H12N2O5
Molecular Weight
240.22
References & Citations
[1]Cysyk RL, et al. Cyclopentenyl uracil: an effective inhibitor of uridine salvage in vivo. Biochem Pharmacol. 1995;49 (2) :203-207.
Shipping Conditions
Blue Ice
Storage Conditions
-20°C, 3 years (Powder)
Scientific Category
Reference compound1
Clinical Information
No Development Reported
Available Sizes
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