Tesaglitazar

Chemical compound
  • None
Legal statusLegal status
  • Development terminated
Identifiers
  • (2S)-2-Ethoxy-3-[4-[2-(4-methylsulfonyloxyphenyl)
    ethoxy]phenyl]propanoic acid
CAS Number
  • 251565-85-2 checkY
PubChem CID
  • 208901
ChemSpider
  • 180999 ☒N
UNII
  • 6734037O3L
KEGG
  • D01274 checkY
ChEMBL
  • ChEMBL521632 ☒N
CompTox Dashboard (EPA)
  • DTXSID4048773 Edit this at Wikidata
ECHA InfoCard100.201.079 Edit this at WikidataChemical and physical dataFormulaC20H24O6SMolar mass392.47 g·mol−13D model (JSmol)
  • Interactive image
  • CCO[C@@H](CC1=CC=C(C=C1)OCCC2=CC=C(C=C2)OS(=O)(=O)C)C(=O)O
InChI
  • InChI=1S/C20H24O6S/c1-3-25-19(20(21)22)14-16-6-8-17(9-7-16)26-13-12-15-4-10-18(11-5-15)27-28(2,23)24/h4-11,19H,3,12-14H2,1-2H3,(H,21,22)/t19-/m0/s1 ☒N
  • Key:CXGTZJYQWSUFET-IBGZPJMESA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Tesaglitazar (also known as AZ 242) is a dual peroxisome proliferator-activated receptor agonist with affinity to PPARα and PPARγ, proposed for the management of type 2 diabetes.[1]

The drug had completed several phase III clinical trials,[2] however in May, 2006 AstraZeneca announced that it had discontinued further development.[3]

Cardiac toxicity of tesaglitazar is related to mitochondrial toxicity caused by decrease in PPARγ coactivator 1-α (PPARGC1A, PGC1α) and sirtuin 1 (SIRT1).[4]

References

  1. ^ Wilding JP, Gause-Nilsson I, Persson A (September 2007). "Tesaglitazar, as add-on therapy to sulphonylurea, dose-dependently improves glucose and lipid abnormalities in patients with type 2 diabetes". Diabetes & Vascular Disease Research. 4 (3): 194–203. doi:10.3132/dvdr.2007.040. PMID 17907109. S2CID 896195.
  2. ^ "GALIDA (tesaglitazar) Clinical Trial Report Summaries". AstraZeneca. Retrieved 2008-03-17. [dead link]
  3. ^ "AstraZeneca Discontinues Development of GALIDA (tesaglitazar)". AstraZeneca. 2006-05-04. Retrieved 2012-07-23.
  4. ^ Kalliora C, Kyriazis ID, Oka SI, Lieu MJ, Yue Y, Area-Gomez E, et al. (August 2019). "Dual peroxisome-proliferator-activated-receptor-α/γ activation inhibits SIRT1-PGC1α axis and causes cardiac dysfunction". JCI Insight. 5 (17). doi:10.1172/jci.insight.129556. PMC 6777908. PMID 31393858.
  • v
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Oral diabetes medication, insulins and insulin analogs, and other drugs used in diabetes (A10)
fast-acting
short-acting
long-acting
ultra-long-acting
inhalable
  • Exubera
  • Afrezza
Non-insulins
Insulin sensitizers
Biguanides
TZDs/"glitazones" (PPAR)
Dual PPAR agonists
Amylin analogs and DACRAs
Secretagogues
K+ATP
Sulfonylureas
Meglitinides/"glinides"
GLP-1 receptor agonists
GLP1 poly-agonist peptides
DPP-4 inhibitors/"gliptins"
Other
Aldose reductase inhibitors
Alpha-glucosidase inhibitors
SGLT2 inhibitors/"gliflozins"
Other
Combinations
  • v
  • t
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PPARTooltip Peroxisome proliferator-activated receptor modulators
PPARαTooltip Peroxisome proliferator-activated receptor alpha
PPARδTooltip Peroxisome proliferator-activated receptor delta
  • Antagonists: FH-535
  • GSK-0660
  • GSK-3787
PPARγTooltip Peroxisome proliferator-activated receptor gamma
  • SPPARMsTooltip Selective PPARγ modulator: BADGE
  • EPI-001
  • INT-131
  • MK-0533
  • S26948
  • Antagonists: FH-535
  • GW-9662
  • SR-202
  • T-0070907
  • Unknown: SR-1664
Non-selective
See also
Receptor/signaling modulators
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