SML0032

Triacetyl resveratrol

≥98% (HPLC)

• Synonym(s): 3,5,4′-Tri-O-acetylresveratrol, 5-[(1E)-2-[4-(acetyloxy)phenyl]ethenyl]-1,3-Benzenediol-1,3-diacetate
• Empirical Formula (Hill Notation): C₂₀H₁₈O₆
• CAS Number: 42206-94-0
• Molecular Weight: 354.35
• NACRES: NA.25
• PubChem Substance ID: 329825102
• UNSPSC Code: 12352200
• MDL number: MFCD01546481

Properties

• Quality Segment: 100
• assay: ≥98% (HPLC)
• form: powder
• storage condition: protect from light
• color: white to tan
• solubility: DMSO: ≥18 mg/mL
• application(s): metabolomics; vitamins, nutraceuticals, and natural products
• storage temp.: room temp
• SMILES string: 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+
• InChI key: PDAYUJSOJIMKIS-SNAWJCMRSA-N

Description

General description

Resveratrol (RSV) is a natural polyphenolic antioxidant.

Biochem/physiol Actions

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.

Resveratrol prodrug. SIRT inhibitor

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.

Safety Information

• Storage Class: 11 - Combustible Solids
• wgk: WGK 3