Troglitazone

CAS No. 97322-87-7

Troglitazone( CS-045 )

Catalog No. M16880 CAS No. 97322-87-7

A PPARγ activator that has antidiabetic, anti-tumor and anti-inflammatory activities.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 73 In Stock
2MG 33 In Stock
5MG 53 In Stock
10MG 86 In Stock
25MG 166 In Stock
50MG 299 In Stock
100MG 547 In Stock
200MG Get Quote In Stock
500MG 1144 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Troglitazone
  • Note
    Research use only, not for human use.
  • Brief Description
    A PPARγ activator that has antidiabetic, anti-tumor and anti-inflammatory activities.
  • Description
    A PPARγ activator that has antidiabetic, anti-tumor and anti-inflammatory activities; binds to PPARγ and selectively induces the early growth response-1 gene expression; inhibits biosynthesis of cholesterol in CHO cell (IC50=8 ug/ml); enhances human lung cancer cells to TRAIL-induced apoptosis via autophagy flux.Diabetes Approved(In Vitro):Troglitazone is a PPARγ agonist, with EC50s of 550 nM and 780 nM for human and murine PPARγ receptor, respectively. Troglitazone (2-200 μM) is cytotoxic to the pancreatic cancer cell lines (MIA Paca2 and PANC-1 cells), with IC50s of 49.9 ± 1.2 and 51.3 ± 5.3 μM, respectively. Troglitazone (50 μM) increases chromatin condensation in MIA Paca2 and PANC-1 cells, enhances the activity of caspase-3 and decreases Bcl-2 expression. Troglitazone (0, 1, 2, and 4 μM) sensitizes TRAIL-mediated apoptosis in human lung adenocarcinoma cells. Troglitazone enhancement of TRAIL-induced apoptosis is blocked by inhibition of autophagy, via activation of autophagy flux. In addition, the effects of troglitazone are induced by PPARγ activation in A549 cells.(In Vivo):Troglitazone (200 mg/kg, p.o.) shows inhibitory effects on the growth of tumor in the MIA Paca2 xenograft model.
  • In Vitro
    Troglitazone is a PPARγ agonist, with EC50s of 550 nM and 780 nM for human and murine?PPARγ receptor, respectively. Troglitazone (2-200 μM) is cytotoxic to the pancreatic cancer cell lines (MIA Paca2 and PANC-1 cells), with IC50s of 49.9?±?1.2 and 51.3?±?5.3 μM, respectively. Troglitazone (50 μM) increases chromatin condensation in MIA Paca2 and PANC-1 cells, enhances the activity of caspase-3 and decreases Bcl-2 expression. Troglitazone (0, 1, 2, and 4 μM) sensitizes TRAIL-mediated apoptosis in human lung adenocarcinoma cells. Troglitazone enhancement of TRAIL-induced apoptosis is blocked by inhibition of autophagy. In addition, the effects of troglitazone are induced by PPARγ activation in A549 cells.
  • In Vivo
    Troglitazone (200 mg/kg, p.o.) shows inhibitory effects on the growth of tumor in the MIA Paca2 xenograft model.
  • Synonyms
    CS-045
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    PPAR
  • Recptor
    PPARγ
  • Research Area
    Metabolic Disease
  • Indication
    Diabetes

Chemical Information

  • CAS Number
    97322-87-7
  • Formula Weight
    441.5399
  • Molecular Formula
    C24H27NO5S
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    O=C(N1)SC(CC2=CC=C(OCC3(C)CCC4=C(C)C(O)=C(C)C(C)=C4O3)C=C2)C1=O
  • Chemical Name
    2,4-Thiazolidinedione, 5-[[4-[(3,4-dihydro-6-hydroxy-2,5,7,8-tetramethyl-2H-1-benzopyran-2-yl)methoxy]phenyl]methyl]-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Baek SJ, et al. J Biol Chem. 2003 Feb 21;278(8):5845-53. 2. Nazim UM, et al. Oncotarget. 2017 Apr 18;8(16):26819-26831. 3. Wang M, et al. Diabetes. 1999 Feb;48(2):254-60.
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