Odevixibat

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

Odevixibat
For small sizes, please check our retail website as below: www.invivochem.com
Size Price Stock
50mg$700To Be Confirmed
100mg$1200To Be Confirmed
200mg$1800To Be Confirmed

Cat #: V9853 CAS #: 501692-44-0 Purity ≥ 98%

Description: Odevixibat (formerly known as A-4250; AZD-8294; A-4250; AR-H 064974; Bylvay) is a novel, potent and orally bioavailable inhibitor of ileal bile acid transporter (IBAT) with the potential to be used for the treatment of primary biliary cirrhosis.

References: Baghdasaryan A, et al. Inhibition of intestinal bile acid absorption improves cholestatic liver and bile duct injury in a mouse model of sclerosing cholangitis.J Hepatol. 2016 Mar;64(3):674-81.

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Product Promise

Promise
Molecular Weight (MW)740.93
Molecular FormulaC37H48N4O8S2
CAS No.501692-44-0
SynonymsAZD8294; A4250; AR-H064974; AZD-8294; A-4250; AR-H-064974
ProtocolIn VivoOdevixibat (A4250)(0.01% (w/w) in chow diet; 4 weeks) improves sclerosing cholangitis and significantly reduces serum alanine aminotransferase, alkaline phosphatase and BAs levels, hepatic expression of pro-inflammatory and pro-fibrogenic genes and bile duct proliferation in Mdr2-/- mice
Animal model Eight week old Mdr2-/- (Abcb4-/-) mice (model of cholestatic liver injury and sclerosing cholangitis)
Dosages0.01% (w/w) in chow diet
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
1mM1.3497 mL6.7483 mL13.4966 mL26.9931 mL
5mM0.2699 mL1.3497 mL2.6993 mL5.3986 mL
10mM0.1350 mL0.6748 mL1.3497 mL2.6993 mL
20mM0.0675 mL0.3374 mL0.6748 mL1.3497 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.