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trans-Resveratrol-3-O-β-D-Glucuronide

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    <em>trans</em>-Resveratrol-3-O-β-D-Glucuronide
  • <em>trans</em>-Resveratrol-3-O-β-D-Glucuronide
Cat No: 13832
Biochemicals - Analytical Standards
Cayman
€228.00
Price is excluding VAT and does not include packaging neither shipping

Resveratrol is a potent phenolic antioxidant found in grapes and red wine that also has antiproliferative and anti-inflammatory activity.{9146} In humans, resveratrol is almost completely conjugated to its glucuronide and sulfate metabolites.{12177} tr...

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This product can only be bought through Cayman Chemical. Please contact us.

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Territorial Availability: Available through Bertin Technologies only in Europe
Synonyms:
  • 3-hydroxy-5-[(1E)-2-(4-hydroxyphenyl)ethenyl]phenyl-β-D-glucopyranosiduronic acid
Correlated keywords:
  • 1028964-58-0 regioisomer resveratrol metabolite analytical reference standard metabolism biochemical antioxidant inflammation metabolism trans-resveratrol 3-O-glucuronide 3-glucuronide 3'-glucuronide phenolic grape red wine antiproliferative anti-proliferative anti-inflammatory antiinflammatory glucuronide sulfate conjugate regioisomeric determination metabolic profile trans-Resveratrol-3-O-β-D-Glucuronide
Product Overview:
Resveratrol is a potent phenolic antioxidant found in grapes and red wine that also has antiproliferative and anti-inflammatory activity.{9146} In humans, resveratrol is almost completely conjugated to its glucuronide and sulfate metabolites.{12177} trans-Resveratrol-3-O-β-D-glucuronide is a regioisomeric resveratrol metabolite that may be used as a reference standard for accurate determination of the metabolic profile of resveratrol.
Size 500 µg
Shipping dry ice
Stability Store at -20 degrees; shelf life 730 days
CAS Number 387372-17-0
Molecular Formula C20H20O9
SMILES O[C@H]1[C@H](O)[C@@H](O)[C@H](OC2=CC(/C=C/C3=CC=C(O)C=C3)=CC(O)=C2)O[C@@H]1C(O)=O
Molecular Weight 404,4
Formulation A crystalline solid
Purity ≥95%
Custom Code 2932.99
UNSPSC code 12352100

Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

Accreditations
ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.

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