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Key Documents

SMB00348

Sigma-Aldrich

Ginsenoside Compound K

≥96% (HPLC)

Sinonimo/i:

(3B,12B)-3,12-Dihydroxydammar-24-en-20-yl β-D-glucopyranoside, 20(S)-Ginsenoside Ck, Ginsenoside K, Protopanaxadiol 20-O-glucoside

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About This Item

Formula empirica (notazione di Hill):
C36H62O8
Numero CAS:
Peso molecolare:
622.87
Codice UNSPSC:
12352205
ID PubChem:
NACRES:
NA.25

Saggio

≥96% (HPLC)

Forma fisica

powder

applicazioni

metabolomics
vitamins, nutraceuticals, and natural products

Stringa SMILE

CC(C)=CCC[C@](C1C2[C@H](O)CC3[C@@]([C@]2(C)CC1)(C)CCC4C(C)(C)[C@@H](O)CC[C@@]43C)(C)O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O

InChI

1S/C36H62O8/c1-20(2)10-9-14-36(8,44-31-30(42)29(41)28(40)23(19-37)43-31)21-11-16-35(7)27(21)22(38)18-25-33(5)15-13-26(39)32(3,4)24(33)12-17-34(25,35)6/h10,21-31,37-42H,9,11-19H2,1-8H3/t21?,22-,23-,24?,25?,26+,27?,28-,29+,30-,31+,33+,34-,35-,36+/m1/s1
FVIZARNDLVOMSU-KJULZEBLSA-N

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Descrizione generale

Ginsenoside Compound K is a tetracyclic dammarane-type triterpenoid saponin found in the roots of Panax ginseng. It is a major constituent in ginseng, which has been traditionally used to increase resistance to stress and aging.

Applicazioni


  • Combination of Electrochemistry and Mass Spectrometry to Study Nitric Oxide Metabolism and Its Modulation by Compound K in Breast Cancer Cells.: This research explores the interaction of Ginsenoside Compound K with nitric oxide metabolism in breast cancer cells, employing a combination of electrochemical techniques and mass spectrometry to elucidate the metabolic pathways and potential therapeutic effects of Compound K (Zhao et al., 2022).

  • Metabolic analysis of Panax notoginseng saponins with gut microbiota-mediated biotransformation by HPLC-DAD-Q-TOF-MS/MS.: This article investigates the gut microbiota-mediated biotransformation of Panax notoginseng saponins, including Compound K, detailing the complex interactions and metabolic profiles in a biological system, which could inform their therapeutic use and bioavailability (Chen et al., 2018).

Azioni biochim/fisiol

Ginsenoside compound K has many pharmacological properties that include anti-diabetic, anti-inflammatory, hepatoprotective, anti-allergic, and anti-carcinogenic effects. It also displays neuroprotective properties, in mice it has shown recovery from synaptic loss and memory impairment. Ginsenoside K can inhibit several gene expressions in human umbilical vein endothelial cells (HUVECs), resulting in the inhibition of migration and angiogenesis of endothelial cells.

Pittogrammi

Exclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 4 Oral

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


Certificati d'analisi (COA)

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Catherine Hu et al.
European journal of pharmacology, 815, 501-511 (2017-10-17)
Conflicting data exist on the effect of ginsenosides on transactivation of human glucocorticoid receptor α (herein referred to as glucocorticoid receptor), and relatively little is known regarding the effect of these chemicals on transrepression of this receptor. We investigated the

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