Ginsenoside Rb1

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Ginsenoside Rb₁

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Cat No: 15319

Biochemicals - Kinase Inhibitors

Ginsenosides are pharmacologically active natural compounds from ginseng and other plants of the genus Panax.{24877} Structurally, they are steroid glycosides derived from the triterpene squalene.{24877} They are named according to their migration on t...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

20-[(6-O-?-D-glucopyranosyl-?-D-glucopyranosyl)oxy]-12?-hydroxydammar-24-en-3?-yl 2-O-?-D-glucopyranosyl-?-D-glucopyranoside

Correlated keywords:

12770-?17-?1 52286-?61-?0 87700-?07-?0 212055-?66-?8 393829-?67-?9 natural products neurosciences inflammation obesity apoptosis ginesosides ginseng plants genus panax protopanaxadiol species P. quinquefolium in vitro vivo neuroprotective anti-inflammatory anti inflammatory antiinflammatory anti-obesity obesity antiobesity steroids Rb1 arasaponin E1 gynosaponin C gypenoside III NSCs 310103 NSC-310103 NSC310103 notoginsenoside panaxoside sanchinoside glycosides triterpenes squalene p-38 A?-40 NF?B

Product Overview:
Ginsenosides are pharmacologically active natural compounds from ginseng and other plants of the genus Panax.{24877} Structurally, they are steroid glycosides derived from the triterpene squalene.{24877} They are named according to their migration on thin layer chromatography plates, from the bottom to the top.{24877} Ginsenoside Rb1 is a protopanaxadiol, which is more abundant in some Panax species (e.g., P. quinquefolium) than others.{24880} This ginsenoside and its metabolites have diverse in vitro and in vivo effects, including neuroprotective, anti-inflammatory, and anti-obesity actions.{24880,24876,24875} Ginsenoside Rb1 may inhibit apoptosis, while its metabolites can promote this response.{24876,24878} Notably, this ginsenoside is converted to other forms in response to steaming or heating plant materials, leading to loss of activity.{24880,24879}

Size	5 mg
Shipping	dry ice
CAS Number	41753-43-9
Molecular Formula	C₅₄H₉₂O₂₃
SMILES	O[C@H]1[C@@]2([H])[C@](CC[C@]2([H])[C@@](CC/C=C(C)/C)(C)O[C@@H]3O[C@H](CO[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O4)[C@@H](O)[C@H](O)[C@H]3O)(C)[C@]5(C)CC[C@]6([H])[C@@](CC[C@H](O[C@]7([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]7O[C@@]8([H])[C@H](O)[C@@H](O)[C@
Molecular Weight	1109,3
Formulation	A crystalline solid
Purity	≥98%
Custom Code	2906.13
UNSPSC code	12352100

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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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