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 |
| 2MG | 32 | In Stock |
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| 5MG | 50 | In Stock |
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| 10MG | 81 | In Stock |
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| 25MG | 158 | In Stock |
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| 50MG | 290 | In Stock |
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| 100MG | 529 | In Stock |
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| 500MG | 1107 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameTroglitazone
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NoteResearch use only, not for human use.
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Brief DescriptionA PPARγ activator that has antidiabetic, anti-tumor and anti-inflammatory activities.
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DescriptionA 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.
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In VitroTroglitazone 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.
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In VivoTroglitazone (200 mg/kg, p.o.) shows inhibitory effects on the growth of tumor in the MIA Paca2 xenograft model.
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SynonymsCS-045
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PathwayMetabolic Enzyme/Protease
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TargetPPAR
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RecptorPPARγ
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Research AreaMetabolic Disease
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IndicationDiabetes
Chemical Information
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CAS Number97322-87-7
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Formula Weight441.5399
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Molecular FormulaC24H27NO5S
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESO=C(N1)SC(CC2=CC=C(OCC3(C)CCC4=C(C)C(O)=C(C)C(C)=C4O3)C=C2)C1=O
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Chemical Name2,4-Thiazolidinedione, 5-[[4-[(3,4-dihydro-6-hydroxy-2,5,7,8-tetramethyl-2H-1-benzopyran-2-yl)methoxy]phenyl]methyl]-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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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