Ginsenoside Rg2

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Ginsenoside Rg₂

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Cat No: 15331

Biochemicals - Lipids

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} Ginsenoside Rg2 is a protopanaxatriol that is mo...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

(6?)-3?,12?,20-trihydroxydammar-24-en-6-yl 2-O-(6-deoxy-?-L-mannopyranosyl)-?-D-glucopyranoside

Correlated keywords:

12770-?18-?2 naturals products neurosciences inflammation diabetes DNA damages apoptosis ginsenosides Rg-2 Rgs 2 two protopanaxatriol in vitro in vivo neuroprotectives anti-inflammatory antiinflammatory anti inflammatory anti-diabetic diabetic antidiabetic protects protections protected against UVs ultraviolet lights deoxyribonucleic acids steroids glycosides diverse chikusetsusaponin I GFs GFVI VI GF-VI 20-Rg2 panaxoside Rg2 prosapogenin C2 S-ginsenoside panax R. quinquefolium pharmacologically actives compounds ginseng plants genus Panax triterpenes squalenes whites reds P. metabolites induced bioactive steaming heating materials quinquefolium P.quinquefolum P.ginseng

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} Ginsenoside Rg2 is a protopanaxatriol that is more abundant in some Panax species (e.g., white and red P. ginseng) than others.{24880} This ginsenoside and its metabolites have diverse in vitro and in vivo effects, including neuroprotective, anti-inflammatory, and anti-diabetic actions.{25809,25807,25808} It also protects against DNA damage and apoptosis induced by ultraviolet light.{25810} Notably, this ginsenoside is increased by the metabolism of other bioactive ginsenosides during the steaming or heating of plant materials, particularly in P. quinquefolium.{24880,24879}

Size	500 µg
Shipping	dry ice
CAS Number	52286-74-5
Molecular Formula	C₄₂H₇₂O₁₃
SMILES	O[C@H]1[C@@]2([H])[C@](CC[C@]2([H])[C@@](CC/C=C(C)/C)(C)O)(C)[C@]3(C)C[C@H](O[C@@]4([H])[C@H](O[C@@]5([H])[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O5)[C@@H](O)[C@H](O)[C@@H](CO)O4)[C@]6([H])[C@@](CC[C@H](O)C6(C)C)(C)[C@@]3([H])C1
Molecular Weight	785
Formulation	A crystalline solid
Purity	≥98%
Custom Code	2932.99
UNSPSC code	12352100

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