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Ginsenoside Rg5

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    Ginsenoside Rg<sub>5</sub>
  • Ginsenoside Rg<sub>5</sub>
Cat No: 25147
Biochemicals - Natural Products
Cayman

Ginsenoside Rg5 is a ginsenoside originally isolated from P. ginseng that has diverse biological activities, including anticancer, anti-inflammatory, neuroprotective, and antioxidant properties.{39967,39968,39969} It inhibits the growth of HeLa and MS...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • (3?,12?,20E)-12-hydroxydammara-20(22),24-dien-3-yl 2-O-?-D-glucopyranosyl-?-D-glucopyranoside
Correlated keywords:
  • Rg-5 Panax cancer antiinflammatory oxidant MS-751 IL1? 1-? TNF? COX2 Rg5E 5-E lipopolysaccharide cyclooxygenase
Product Overview:
Ginsenoside Rg5 is a ginsenoside originally isolated from P. ginseng that has diverse biological activities, including anticancer, anti-inflammatory, neuroprotective, and antioxidant properties.{39967,39968,39969} It inhibits the growth of HeLa and MS751 cervical cancer cells (IC50s = ~2.5-10 μM) and induces apoptosis in a concentration-dependent manner.{39967} Ginsenoside Rg5 (5 and 10 μM) inhibits LPS-induced increases in IL-1β, TNF-α, COX-2, and inducible nitric oxide synthase (iNOS) protein levels in murine alveolar macrophages.{39968} It also inhibits LPS-induced increases in the number of neutrophils and protein levels of IL-1β, TNF-α, COX-2, and iNOS in lung in a mouse model of acute lung inflammation when administered at a dose of 10 mg/kg. In a rat model of Alzheimer's disease induced by streptozotocin (STZ; Item No. 13104), ginsenoside Rg5 blocks STZ-induced increases in amyloid-β accumulation in the hippocampus and cerebral cortex and prevents STZ-induced decreases in step through latency time in a passive avoidance foot-shock test in a dose-dependent manner.{39969}
Size 1 mg
Shipping dry ice
CAS Number 186763-78-0
Molecular Formula C42H70O12
SMILES O[C@H]1[C@@]2([H])[C@](CC[C@@H]2/C(C)=C/C/C=C(C)\C)(C)[C@]3(C)CC[C@]4([H])[C@@](CC[C@H](O[C@]5([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O[C@@]6([H])[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O6)C4(C)C)(C)[C@@]3([H])C1
Molecular Weight 767
Formulation A crystalline solid
Purity ≥95%
Custom Code 2932.99
UNSPSC code 12352100

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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.

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