tranilast

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

tranilast
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Size Price Stock
1g$300Check With Us
2g$450Check With Us
5g$680Check With Us

Cat #: V3309 CAS #: 53902-12-8 Purity ≥ 98%

Description: Tranilast (also known as MK 341; SB 252218; trade name Rizaben), an analog of a tryptophan metabolite, is an antiallergic drug developed by Kissei Pharmaceuticals and was approved in 1982 for use in Japan and South Korea for bronchial asthma.

References: M Isaji , et al. Tranilast Inhibits the Proliferation, Chemotaxis and Tube Formation of Human Microvascular Endothelial Cells in Vitro and Angiogenesis in Vivo. Br J Pharmacol. 1997 Nov;122(6):1061-6.

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Product Promise

Promise
Molecular Weight (MW)327.34
Molecular FormulaC18H17NO5
CAS No.53902-12-8
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: ≥ mg/mLr
Water: N/Ar
Ethanol: N/A
SMILES CodeCOC1=C(C=C(C=C1)/C=C/C(=O)NC2=CC=CC=C2C(=O)O)OC
SynonymsMK-341; MK 341; MK341; SB-252218; SB 252218; SB252218; Tranilast; trans-Tranilast; brand name: Rizaben; Tranilastum; Tranpro.
ProtocolIn VitroTranilast (12.5, 25, 50, 100 μg/mL; 72 hours) inhibits proliferation of HDMECs
In VivoTranilast (300 mg/kg; administered orally twice a day for 3 days) dose-dependently suppresses angiogenesis in mice
Animal modelNine-week-old male C57BL/6 mice
Dosages 300 mg/kg
Administration Administered orally twice a day for 3 days
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
1mM3.0549 mL15.2746 mL30.5493 mL61.0986 mL
5mM0.6110 mL3.0549 mL6.1099 mL12.2197 mL
10mM0.3055 mL1.5275 mL3.0549 mL6.1099 mL
20mM0.1527 mL0.7637 mL1.5275 mL3.0549 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.