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3,4?-5-Trihydroxystilbene-3-?-D-Glucopyranoside

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    3,4?-5-Trihydroxystilbene-3-?-D-Glucopyranoside
  • 3,4?-5-Trihydroxystilbene-3-?-D-Glucopyranoside
Cat No: 21246
Biochemicals - Lipids
Cayman

3,4′-5-Trihydroxystilbene-3-β-D-glucopyranoside is a stilbene glucoside that has been found in V. vinifera and has diverse biological activities.{62154,34020,34021,61372,34022} It reduces the growth of SKOV3 ovarian cancer cell 3D aggregates in a conc...

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

Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 3-hydroxy-5-[2-(4-hydroxyphenyl)ethenyl]phenyl ?-D-glucopyranoside
Correlated keywords:
  • anti-pyretic oxidant 3-b-mono 3-O-b-D 3-b-D pediomelum IL17 GPX
Product Overview:
3,4′-5-Trihydroxystilbene-3-β-D-glucopyranoside is a stilbene glucoside that has been found in V. vinifera and has diverse biological activities.{62154,34020,34021,61372,34022} It reduces the growth of SKOV3 ovarian cancer cell 3D aggregates in a concentration-dependent manner.{34020} 3,4′-5-Trihydroxystilbene-3-β-D-glucopyranoside (10 and 20 µg/ml) inhibits IL-17 production in activated peripheral blood mononuclear cells (PBMCs).{34021} It inhibits the loss of glutathione peroxidase 4 (GPX4) activity induced by the ferroptosis inducer hemin in Neuro2a neuroblastoma cells.{61372} 3,4′-5-Trihydroxystilbene-3-β-D-glucopyranoside (50 mg/kg) reduces escape latency in a rat model of vascular dementia induced by four-vessel occlusion (4-VO).{34022}
Size 1 g
Shipping dry ice
CAS Number 65914-17-2
Molecular Formula C20H22O8
SMILES O[C@H]([C@@H](O)[C@@H]1O)[C@@H](O[C@@H]1CO)OC2=CC(C=CC3=CC=C(O)C=C3)=CC(O)=C2
Molecular Weight 390,4
Formulation A crystalline solid
Purity ≥98% (mixture of isomers)
Custom Code 2907.19
UNSPSC code 12352100

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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.

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