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Tranilast

SKU: orb1305160

Description

Tranilast (SB 252218) is an antiallergic agent that inhibits the release of pro-inflammatory lipid mediators and cytokines from various cell types. Its mechanism supports research into allergic diseases, fibrosis, and restenosis, with applications in both in vitro cellular assays and in vivo animal models.

Research Area

Pharmacology & Drug Discovery

Images & Validation

Key Properties

CAS Number53902-12-8
MW327.33
Purity>99.99% (May vary between batches)
FormulaC18H17NO5
SMILESN(C(C=CC1=CC(OC)=C(OC)C=C1)=O)C2=C(C(O)=O)C=CC=C2
TargetRAAS,Prostaglandin Receptor
Solubility10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (6.11 mM);DMSO:50 mg/mL (152.75 mM)

Bioactivity

Target IC50
PGD2:0.1 mM (IC50)
In Vivo
In hypertrophic and proliferative scar tissues, Tranilast ([3-300 mM]) inhibits collagen synthesis in fibroblasts by suppressing the Transforming Growth Factor (TGF)-β1, yet it does not inhibit the fibroblasts in normal skin.
In Vitro
In diabetic rats' hearts, Tranilast reduces the phosphorylation of Smad2, effectively mitigating cardiac fibrosis.

Storage & Handling

Storagekeep away from direct sunlight,store under nitrogen | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

microvascular, MK 341, MK341, MK-341, inhibit, Inhibitor, endothelial, factor, growth, chemotaxis, anti-atopic, Angiogenesis, Angiotensin Receptor, Tranilast, SB 252218, SB252218, SB-252218, Prostaglandin Receptor, ProstaglandinReceptor, prostaglandin, proliferation, vascular, tube

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Quality Guarantee

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Key Properties

No computed properties available.

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Tranilast (orb1305160)

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

Select a size below

5 mg
$ 80.00
1 ml x 10 mM (in DMSO)
$ 90.00
10 mg
$ 90.00
25 mg
$ 110.00
50 mg
$ 130.00
100 mg
$ 170.00
200 mg
$ 230.00
500 mg
$ 360.00
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