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Chemical Structure

Pterostilbene

CDX-P0234
Chemodex
CAS Number537-42-8
Product group Chemicals
Estimated Purity>97%
Molecular Weight256.3
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Overview

  • Supplier
    Chemodex
  • Product Name
    Pterostilbene [537-42-8]
  • Delivery Days Customer
    10
  • CAS Number
    537-42-8
  • Certification
    Research Use Only
  • Estimated Purity
    >97%
  • Hazard Information
    Danger,Excepted quantity
  • Molecular Formula
    C16H16O3
  • Molecular Weight
    256.3
  • Scientific Description
    Cell permeable natural methoxylated analog of resveratrol. Antioxidant, antiproliferative, anti-inflammatory, anti-hyperglycemic and anti-diabetic agent. Induces apoptosis. Induces Autophagy. Pterostilbene is a naturally-occurring dimethyl ether analog of resveratrol that is abundant in blueberries. Like resveratrol, pterostilbene acts as a powerful antioxidant, suppresses the synthesis of prostaglandin E2 from lipopolysaccharide-stimulated human peripheral blood mononuclear cells (IC50 = 1.0 microM for pterostilbene, 3.2 microM for resveratrol), and inhibits cell proliferation (IC50 = ~60 microM for both compounds). Very potent inhibitor of cytochrome P450 1A1 (CYP1A1) with Ki=0.57microM. Pterostilbene blocks the activation of ERK1/2, p38 MAPK, and PI3K/Akt signaling pathways, reducing NF-kappaB and AP-1 transcriptional activation. Moderately inhibits COX-1 and COX-2 (IC50=19.8microM and 83.9microM). - Chemical. CAS: 537-42-8. Formula: C16H16O3. MW: 256.3. Synthetic. Cell permeable natural methoxylated analog of resveratrol. Antioxidant, antiproliferative, anti-inflammatory, anti-hyperglycemic and anti-diabetic agent. Induces apoptosis. Induces Autophagy. Pterostilbene is a naturally-occurring dimethyl ether analog of resveratrol that is abundant in blueberries. Like resveratrol, pterostilbene acts as a powerful antioxidant, suppresses the synthesis of prostaglandin E2 from lipopolysaccharide-stimulated human peripheral blood mononuclear cells (IC50 = 1.0 microM for pterostilbene, 3.2 microM for resveratrol), and inhibits cell proliferation (IC50 = ~60 microM for both compounds). Very potent inhibitor of cytochrome P450 1A1 (CYP1A1) with Ki=0.57microM. Pterostilbene blocks the activation of ERK1/2, p38 MAPK, and PI3K/Akt signaling pathways, reducing NF-kappaB and AP-1 transcriptional activation. Moderately inhibits COX-1 and COX-2 (IC50=19.8microM and 83.9microM).
  • SMILES
    OC(C=C1)=CC=C1/C=C/C2=CC(OC)=CC(OC)=C2
  • Storage Instruction
    2°C to 8°C
  • UN Number
    UN3077
  • UNSPSC
    12352200

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