AdipoGen Life Sciences

GW1929

CHF 60.00
In stock
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Product Details
Synonyms N-(2-Benzoylphenyl)-L-tyrosine PPARγ Agonist; (2S)-((2-Benzoylphenyl)amino-3-[4-[2-(methylpyridin-2-ylamino)ethoxy]phenyl]propionic acid
Product Type Chemical
Properties
Formula

C30H29N3O4

MW 495.6
CAS 196808-24-9
Purity Chemicals ≥98% (HPLC)
Appearance Off-white to yellow crystalline solid.
Solubility Soluble in DMSO or methanol.
Identity Determined by 1H-NMR.
InChi Key QTQMRBZOBKYXCG-MHZLTWQESA-N
Smiles COC1=CC(=O)OC(=C1)C1C2(O)CC3OC(=O)[C@]2(O)C(C(=O)C2=CC=CC=C2)C1(O)C3O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Protect from light.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Store solutions at -20°C in the dark.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description
  • Potent and subtype-selective (>1'000-fold) PPARγ agonist [1].
  • Angiogenesis inhibitor [3].
  • Apoptosis inhibitor [4].
  • Anti-inflammatory [4].
  • Anti-hyperglycemic and anti-hyperlipidemic agent [1].
  • Antidiabetic. The glucose-lowering effect in rats is 100-fold more potent than that of troglitazone [2].
Product References
  1. N-(2-Benzoylphenyl)-L-tyrosine PPARgamma agonists. 1. Discovery of a novel series of potent antihyperglycemic and antihyperlipidemic agents: B.R. Henke, et al.; J. Med. Chem. 41, 5020 (1998)
  2. A novel N-aryl tyrosine activator of peroxisome proliferator-activated receptor-gamma reverses the diabetic phenotype of the Zucker diabetic fatty rat: K.K. Brown, et al.; Diabetes 48, 1415 (1999)
  3. PPARgamma agonists inhibit angiogenesis by suppressing PKCalpha- and CREB-mediated COX-2 expression in the human endothelium: E. Scoditti, et al.; Cardiovasc. Res. 86, 302 (2010)
  4. Ameliorative Effects of GW1929, a Nonthiazolidinedione PPAR γ Agonist, on Inflammation and Apoptosis in Focal Cerebral Ischemic-Reperfusion Injury: R.K. Kaundal & S.S. Sharma; Curr. Neurovasc. Res. 8, 236 (2011)
  5. Reactive fibrosis precedes doxorubicin-induced heart failure through sterile inflammation: R. Tanaka, et al.; ESC Heart Fail. ahead of print (2020)
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