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Troglitazone

Troglitazone

Product ID T7056
Cas No. 97322-87-7
Purity ≥97%
Product Unit SizeCostQuantityStock
10 mg $134.30 In stock
50 mg $515.90 In stock
100 mg $763.70 In stock
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Quicklinks

  • Description
  • Product Info
  • Shipping and Storage
  • Downloads
  • References
  • Description
  • Product Info
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  • Downloads
  • References
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Description

Troglitazone is a thiazolidinedione PPARγ agonist that exhibits anti-diabetic, anticancer, anti-fibrotic, and anti-inflammatory activities. Troglitazone contains a vitamin E-like ring structure that forms hepatotoxic metabolites in vivo. Troglitazone induces apoptosis in cervical cancer cells and decreases expression and activity of telomerase in ER- breast cancer cells. In vitro, troglitazone activates AMPK, decreases membrane potential, inhibits high glucose-closed ATP-sensitive K+ channels, and decreases insulin hypersecretion. In alveolar epithelial cells, troglitazone inhibits TGF-β1-induced activation of Akt, GSK-3β and Smad2/3, decreases β-catenin signaling, and suppresses epithelial-to-mesenchymal transition (EMT). Additionally, this compound inhibits PAM-induced increases in TGF-β1 and increases MUC1 expression in airway epithelial cells.

Product Info

Cas No.

97322-87-7

Purity

≥97%

Formula

C24H27NO5S

Formula Wt.

441.54

Chemical Name

5-[[4-[(3,4-Dihydro-6-hydroxy-2,5,7,8-tetramethyl- 2H-1-benzopyran-2-yl)methoxy]phenyl]methyl]-2,4- thiazolidinedione

IUPAC Name

5-[[4-[(6-hydroxy-2,5,7,8-tetramethyl-3, 4-dihydrochromen-2-yl)methoxy]phenyl]methyl]-1,3-thiazolidine-2,4-dione

Synonym

Noscal, Prelay, Rezulin, Romozin

Melting Point

184-186°C

Solubility

Soluble in DMSO 15mg/mL, and dimethyl formide. Slightly soluble in 100% ethanol (warm).

Appearance

Yellow Solid

Shipping and Storage

Store Temp

Ambient

Ship Temp

Ambient

Downloads

MSDS

T7056 MSDS PDF

Info Sheet

T7056 Info Sheet PDF

Brochures

WNT Booklet

References

Chen HM, Zhang DG, Wu JX, et al. Ubiquitination of p53 is involved in troglitazone induced apoptosis in cervical cancer cells. Asian Pac J Cancer Prev. 2014;15(5):2313-8. PMID: 24716976.

Deng R, Nie A, Jian F, et al. Acute exposure of beta-cells to troglitazone decreases insulin hypersecretion via activating AMPK. Biochim Biophys Acta. 2014 Jan;1840(1):577-85. PMID: 24144566.

Zhou B, Buckley ST, Patel V, et al. Troglitazone attenuates TGF-β1-induced EMT in alveolar epithelial cells via a PPARγ-independent mechanism. PLoS One. 2012;7(6):e38827. PMID: 22745681.

Park YS, Lillehoj EP, Kato K, et al. PPARγ inhibits airway epithelial cell inflammatory response through a MUC1-dependent mechanism. Am J Physiol Lung Cell Mol Physiol. 2012 Apr 1;302(7):L679-87. PMID: 22268120.

Rashid-Kolvear F, Taboski MA, Nguyen J, et al. Troglitazone suppresses telomerase activity independently of PPARgamma in estrogen-receptor negative breast cancer cells. BMC Cancer. 2010 Jul 22;10:390. PMID: 20650001.

Ozaki S, Minamisono T, Yamashita T, et al. Supersaturation-nucleation behavior of poorly soluble drugs and its impact on the oral absorption of drugs in thermodynamically high-energy forms. J Pharm Sci. 2012 Jan;101(1):214-222. PMID: 21918988.

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