VIPADENANT

This product is for research use only, not for human use. We do not sell to patients.

VIPADENANT
For small sizes, please check our retail website as below: www.invivochem.com
Size Price Stock
250mg$700Check With Us
500mg$1150Check With Us
1g$1725Check With Us

Cat #: V3943 CAS #: 442908-10-3 Purity ≥ 98%

Description: Vipadenant (formerly BIIB-014; CEB-4520; V-2006; VER-11135) is a novel potent, selective and orally bioactive antagonist of adenosine A2A receptor with immunomodulatory and antidegenerative effects.

References: Jones N, et al. A2A receptor antagonists do not induce dyskinesias in drug-naive or L-dopa sensitized rats. Brain Res Bull. 2013 Sep;98:163-9.

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Product Promise

Promise
Molecular Weight (MW)321.34
Molecular FormulaC16H15N7O
CAS No.442908-10-3
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: ≥ 30 mg/mLr
Water: N/Ar
Ethanol: N/A
SMILES CodeNC1=NC(C2=CC=CO2)=C(N=NN3CC4=CC=C(N)C(C)=C4)C3=N1
SynonymsCEB-4520; VER-11135; CEB4520; BIIB014; BIIB 014;V-2006; VER-A00-11; VER-A00049; CEB 4520; BIIB-014; V2006; V 2006; VER-ADO-49
ProtocolIn VivoVipadenant (0.3-30 mg/kg) produces a dose-dependent reduction in catalepsy. Vipadenant (10 mg/kg) does not produce any statistically significant dyskinetic episodes in 6-OHDA-lesioned rats during a 19-day dosing regimen
These protocols are for reference only. InvivoChem does not independently validate these methods.
Preparing Stock Solutions
Solvent volume to be added Mass (the weight of a compound)
Mother liquor concentration 1mg5mg10mg20mg
1mM3.1120 mL15.5598 mL31.1197 mL62.2394 mL
5mM0.6224 mL3.1120 mL6.2239 mL12.4479 mL
10mM0.3112 mL1.5560 mL3.1120 mL6.2239 mL
20mM0.1556 mL0.7780 mL1.5560 mL3.1120 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.