SMB00348

Ginsenoside Compound K

≥96% (HPLC)

Manufacturer: Sigma Aldrich

CAS Number: 39262-14-1

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

Select a Size

Pack Size SKU Availability Price
5 MG SMB00348-5-MG In Stock ₹ 20,340.18

SMB00348 - 5 MG

₹ 20,340.18

In Stock

Quantity

1

Base Price: ₹ 20,340.18

GST (18%): ₹ 3,661.232

Total Price: ₹ 24,001.412

Quality Level

200

Assay

≥96% (HPLC)

form

powder

application(s)

metabolomicsvitamins, 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

Other Options

Image Product Name Manufacturer Price Range
11-100-2119
phyproof™ Ginsenoside C-K, ≥95% (HPLC), MilliporeSigma™ Supelco™
MilliporeSigma Supelco ₹ 80,255.28
50-245-6060
eMolecules​ Medchem Express / Ginsenoside C-K / 5mg / 446275532 / HY-N0904 / / 39262-14-1 / MFCD07772261 / 622.884 / C36H62O8
eMolecules​ ₹ 8,186.38
50-186-6556
Sigma Aldrich Fine Chemicals Biosciences Ginsenoside Compound K >=96% (HPLC) | 39262-14-1 | 5MG
Sigma Aldrich Fine Chemicals Biosciences ₹ 23,058.42
PHL80461
Ginsenoside C-K
Sigma Aldrich ₹ 82,995.28
AF57663
39262-14-1 | Ginsenoside CK
A2B Chem ₹ 3,850.20 - ₹ 23,871.24

Description

  • 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.
  • Application: 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).
  • 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.

SAFETY INFORMATION

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Quality Level:
200

Assay:
≥96% (HPLC)

form:
powder

application(s):
metabolomicsvitamins, 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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CN1C[C@@H]2C[C@H](C1)C3=CC=CC(=O)N3C2

InChI:
1S/C12H16N2O/c1-13-6-9-5-10(8-13)11-3-2-4-12(15)14(11)7-9/h2-4,9-10H,5-8H2,1H3/t9-,10+/m0/s1

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CULUKMPMGVXCEI-VHSXEESVSA-N

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OC1=C2C(C(C(O)=C(C3=CC=C(O)C=C3)O2)=O)=C(O)C=C1O

InChI:
1S/C15H10O7/c16-7-3-1-6(2-4-7)14-13(21)12(20)10-8(17)5-9(18)11(19)15(10)22-14/h1-5,16-19,21H

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ZDOTZEDNGNPOEW-UHFFFAOYSA-N

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C[C@@H](C1)[C@H](C)CC2=C(C3=C1C=C(OC)C(OC)=C3OC)C(OC)=C(OC)C(OC)=C2

InChI:
1S/C24H32O6/c1-13-9-15-11-17(25-3)21(27-5)23(29-7)19(15)20-16(10-14(13)2)12-18(26-4)22(28-6)24(20)30-8/h11-14H,9-10H2,1-8H3/t13-,14+

InChI key:
JEJFTTRHGBKKEI-OKILXGFUSA-N