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Ulodesine (BCX4208)

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Ulodesine (BCX4208)
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Cat #: V3307 CAS #: 548486-59-5 Purity ≥ 98%

Description: Ulodesine (formerly also known as BCX4208) is a novel and potent inhibitor of purine nucleoside phosphorylase (PNP) with the potential to be used for the treatment of psoriasis and gout. It inhibits PNP with an IC50 of 0.5 nM. It is currently being developed by Biocryst as a once-daily oral, chronic treatment for gout. Ulodesine acts at the upstream of xanthine oxidase in the purine metabolism pathway to reduce the production of serum uric acid (sUA) by inhibiting PNP. BCX-4208 is currently in early clinical investigation in psoriasis and gout.

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Molecular Weight (MW)264.28
Molecular FormulaC12H16N4O3
CAS No.548486-59-5
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility In VitroDMSO: ≥ 10mg/mL
Water: N/A
Ethanol: N/A
SMILES CodeO=C1C(NC=C2CN3C[C@H](O)[C@@H](CO)C3)=C2N=CN1
SynonymsBCX4208; BCX-4208; BCX 4208; DADMe-immucillin H
Preparing Stock Solutions
Solvent volume to be added Mass (the weight of a compound)
Mother liquor concentration 1mg5mg10mg20mg
1mM3.7839 mL18.9193 mL37.8387 mL75.6773 mL
5mM0.7568 mL3.7839 mL7.5677 mL15.1355 mL
10mM0.3784 mL1.8919 mL3.7839 mL7.5677 mL
20mM0.1892 mL0.9460 mL1.8919 mL3.7839 mL
Quality Control Documentation
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
=
Concentration
×
Volume
×
Molecular Weight*
The dilution calculator equation
Concentration(start) × Volume(start) = Concentration(final) × Volume(final)

This equation is commonly abbreviated as: C1 V1 = C2 V2

Concentration(start)
C1
×
Volume(start)
V1
=
Concentration(final)
C2
×
Volume(final)
V2
Step One: Enter information below
Dosage mg/kg Average weight of animals g Dosing volume per animal µL Number of animals
Step Two: Enter the in vivo formulation
%DMSO + % + %Tween 80 + %ddH2O

Calculation Results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in µL DMSO(Master liquid concentration mg/mL) ,Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation: Take µL DMSO master liquid, next add µL PEG300, mix and clarify, next add µL Tween 80,mix and clarify, next add µL ddH2O,mix and clarify.
Note:
  • (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
  • (2) Be sure to add the solvent(s) in order.