SML0032

Triacetyl resveratrol

≥98% (HPLC)

• Synonyme(s) : 3,5,4′-Tri-O-acetylresveratrol, 5-[(1E)-2-[4-(acetyloxy)phenyl]ethenyl]-1,3-Benzenediol-1,3-diacetate
• Formule empirique (notation de Hill): C₂₀H₁₈O₆
• Numéro CAS: 42206-94-0
• Poids moléculaire : 354.35
• Numéro MDL: MFCD01546481
• Code UNSPSC : 12352200
• ID de substance PubChem : 329825102
• Nomenclature NACRES : NA.25

Propriétés

• Pureté: ≥98% (HPLC)
• Forme: powder
• Conditions de stockage: protect from light
• Couleur: white to tan
• Solubilité: DMSO: ≥18 mg/mL
• Application(s): metabolomics; vitamins, nutraceuticals, and natural products
• Température de stockage: room temp
• Chaîne SMILES: CC(=O)Oc1ccc(cc1)\C=C\c2cc(OC(C)=O)cc(OC(C)=O)c2
• InChI: 1S/C20H18O6/c1-13(21)24-18-8-6-16(7-9-18)4-5-17-10-19(25-14(2)22)12-20(11-17)26-15(3)23/h4-12H,1-3H3/b5-4+
• Clé InChI: PDAYUJSOJIMKIS-SNAWJCMRSA-N

Description

Description générale

Resveratrol (RSV) is a natural polyphenolic antioxidant.

Actions biochimiques/physiologiques

Resveratrol prodrug. SIRT inhibitor
Resveratrol (RSV) plays a protective role on the nervous and cardiovascular systems. It is considered as a modulator of energetic metabolism as it controls glucose homeostasis in obese mice, improves fatty acid oxidation (FAO) and promotes the expression of genes that participate in mitochondrial biogenesis.

Triacetyl resveratrol displays superior bioavailability to the parent compound, resveratrol. The compound induces p53 activity and inhibits proliferation in breast and prostate tumor cell lines.

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3