Tesaglitazar

TargetMol
Product Code: TAR-T17044
Supplier: TargetMol
CodeSizePrice
TAR-T17044-1mg1mg£101.00
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TAR-T17044-5mg5mg£142.00
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TAR-T17044-1mL1 mL * 10 mM (in DMSO)£157.00
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TAR-T17044-10mg10mg£182.00
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TAR-T17044-25mg25mg£286.00
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TAR-T17044-50mg50mg£470.00
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TAR-T17044-100mg100mg£651.00
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TAR-T17044-500mg500mg£1,291.00
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Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃

Images

1 / 1

Further Information

Bioactivity:
Tesaglitazar causes interstitial mesenchymal cell DNA synthesis and fibrosarcomas in subcutaneous tissues in rats. Tesaglitazar is a dual peroxisome proliferator-activated receptor (PPAR) alpha/gamma agonist that is more potent on PPARγ than on PPARα (EC50s: 13.4 μM and 3.6 μM for rat PPARα and human PPARα, respectively).
CAS:
251565-85-2
Formula:
C20H24O7S
Molecular Weight:
408.47
Pathway:
DNA Damage/DNA Repair; Metabolism
Purity:
0.98
SMILES:
CCO[C@@H](Cc1ccc(OCCc2ccc(OS(C)(=O)=O)cc2)cc1)C(O)=O
Target:
PPAR

References

Hellmold H, et al. Tesaglitazar, a PPARalpha/gamma agonist, induces interstitial mesenchymal cell DNA synthesis and fibrosarcomas in subcutaneous tissues in rats. Toxicol Sci. 2007;98(1):63-74. Glinghammar B, et al. Proliferative and molecular effects of the dual PPARalpha/gamma agonist tesaglitazar in rat adipose tissues: relevance for induction of fibrosarcoma. Toxicol Pathol. 2011;39(2):325-336. Osinski V, et al. In vivo liposomal delivery of PPAR?/? dual agonist tesaglitazar in a model of obesity enriches macrophage targeting and limits liver and kidney drug effects. Theranostics. 2020;10(2):585-601. Zhang BC, et al. Tesaglitazar ameliorates non-alcoholic fatty liver disease and atherosclerosis development in diabetic low-density lipoprotein receptor-deficient mice. Exp Ther Med. 2012;4(6):987-992.