WY-14643 (Pirinixic Acid)

WY-14643 (Pirinixic Acid)

Catalog Number:
L002369112APE
Mfr. No.:
APE-A4305
Price:
$188
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      • Overview
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          Background

          WY-14643, also known as Pirinixic Acid, has an agonistic action as peroxisome proliferator-activated receptor (PPAR). It is shown that aliphatic α-substitution of WY-14643 enhances both PPARα and PPARγ agonism. It has been demonstrated that aliphatic substitution in a-position to the carboxylic acid head group of WY-14643 improves both PPARa and PPARg activity and leads to balanced dual PPARa/g agonists in the lower micromolar range, with a-hexyl pirinixic acid as the most active compound. WY-14,643 can moderately elevate the level of TNFa mRNA in the liver. WY-14,643 stimulates production of low levels of hepatic TNFα by Kupffer cells which acts indirectly as a hepatocyte mitogen.

      • Properties
        • Categories
          PPARα agonist, selective and highly potent
          Alternative Name
          WY 14643,WY14643; 2-[4-chloro-6-(2,3-dimethylanilino)pyrimidin-2-yl]sulfanylacetic acid
          CAS Number
          50892-23-4
          Molecular Formula
          C14H14ClN3O2S
          Molecular Weight
          323.8
          Appearance
          A solid
          Purity
          99.71%
          Solubility
          insoluble in H2O; ≥16.2 mg/mL in DMSO; ≥48.8 mg/mL in EtOH with ultrasonic
          Storage
          Store at -20°C
          SMILES
          CC1=C(C(=CC=C1)NC2=CC(=NC(=N2)SCC(=O)O)Cl)C

          * For Research Use Only

      • Reference
        • 1. Tomoki Yagai, Tingting Yan, et al. "Feedback repression of PPARα signaling by Let-7 microRNA." Cell Rep. 2021 Aug 10;36(6):109506. PMID:34380035
          2. Weipeng Hu, Shan Jiang, et al. "High phosphate impairs arterial endothelial function through AMPK‐related pathways in mouse resistance arteries." Acta Physiologica.
          3. Bassem M. Shoucri, Eric S. Martinez, et al. "Retinoid X receptor activation alters the chromatin landscape to commit mesenchymal stem cells to the adipose lineage." Endocrinology. 2017 Jul.

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