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SMB00348

Sigma-Aldrich

Ginsenoside Compound K

≥96% (HPLC)

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Synonym(s):
(3B,12B)-3,12-Dihydroxydammar-24-en-20-yl β-D-glucopyranoside, 20(S)-Ginsenoside Ck, Ginsenoside K, Protopanaxadiol 20-O-glucoside
Empirical Formula (Hill Notation):
C36H62O8
CAS Number:
Molecular Weight:
622.87
PubChem Substance ID:
NACRES:
NA.25

Assay

≥96% (HPLC)

form

powder

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

SMILES string

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

InChI key

FVIZARNDLVOMSU-KJULZEBLSA-N

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This Item
SMB003474498768317
Ginsenoside F1 ≥98% (HPLC)

Sigma-Aldrich

SMB00347

Ginsenoside F1

Ginsenoside Rc analytical standard

Supelco

44987

Ginsenoside Rc

Ginsenoside Rg1 analytical standard

Supelco

68317

Ginsenoside Rg1

form

powder

form

powder

form

-

form

-

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

application(s)

food and beverages

application(s)

food and beverages

Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

100

General description

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.

Biochem/physiol Actions

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.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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25G
Pack Size/Quantity

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705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

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Ginsenoside Rg2 analytical standard

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Effects of sphingolipid metabolism disorders on endothelial cells.
Lai, et al.
Lipids in Health and Disease, 21, 101-101 (2022)
Alzheimer's Disease as a Major Public Health Concern: Role of Dietary Saponins in Mitigating Neurodegenerative Disorders and Their Underlying Mechanisms.
Abduljawad, et al.
Molecules (Basel), 27 (2022)
Xi-Ding Yang et al.
Fitoterapia, 100, 208-220 (2014-12-03)
As an intestinal bacterial metabolite of ginseng protopanaxadiol saponins, ginsenoside compound K (20-O-beta-d-glucopyranosyl-20(S)-protopanaxadiol, CK) is a major deglycosylated metabolite form of ginsenosides which is absorbed into the systemic circulation. And it has demonstrated such diverse intriguing biological properties as anticarcinogenic
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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