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ChemicalBook > Product Catalogue >Biochemical Engineering >Inhibitors >Ginsenoside CK

Ginsenoside CK

Ginsenoside CK Structure
  • ₹18813.85
  • Product name: Ginsenoside CK
  • CAS: 39262-14-1
  • MF: C36H62O8
  • MW: 622.88
  • EINECS:
  • MDL Number:MFCD07772261
  • Synonyms:(20S)-20-(β-D-Glucopyranosyloxy)dammara-24-ene-3β,12β-diol;(20S)-20-O-β-D-Glucopyranosylprotopanaxadiol;20-(β-D-Glucopyranosyloxy)-5α-dammara-24-ene-3β,12β-diol;20-(β-D-Glucopyranosyloxy)dammar-24-ene-3β,12β-diol;IH-901;20(S)-Protopanaxadiol 20-O-D-glucopyranoside;GINSENOSIDE COMPOUND K(P);b-D-Glucopyranoside, (3b,12b)-3,12-dihydroxydaMMar-24-en-20-yl
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Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 5MG
  • ManufacturerSigma-Aldrich(India)
  • Product numberSMB00348
  • Product descriptionGinsenoside Compound K ≥96% (HPLC)
  • Packaging5MG
  • Price₹18813.85
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) SMB00348 Ginsenoside Compound K ≥96% (HPLC) 5MG ₹18813.85 2022-06-14 Buy

Properties

Melting point :181~183℃
Boiling point :723.1±60.0 °C(Predicted)
Density :1.19
solubility :DMF: 10 mg/ml; DMSO: 10 mg/ml; DMSO:PBS (pH 7.2) (1:1): 0.5 mg/ml
pka :12.94±0.70(Predicted)
form :powder
color :White
Stability :Hygroscopic
InChIKey :FVIZARNDLVOMSU-SFEJUJENNA-N
LogP :5.500 (est)

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H302 Harmful if swallowed Acute toxicity,oral Category 4 Warning GHS hazard pictograms P264, P270, P301+P312, P330, P501
Precautionary statements:
P264 Wash hands thoroughly after handling.
P264 Wash skin thouroughly after handling.
P270 Do not eat, drink or smoke when using this product.
P501 Dispose of contents/container to..…

Description

Ginsenoside compound K (C-K) is a metabolite of the protopanaxadiol-type saponins of Panax ginseng C.A. Meyer, has long been used to treat against the development of cancer, inflammation, allergies, and diabetes; C-K acts as a unique HUVEC migration inhibitor by regulating MMP expression, as well as the activity of SPHK1 and its related sphingolipid metabolites. C-K exhibits anti-inflammatory effects by reducing iNOS and COX-2, C-K exhibits an inhibition against the activity of CYP2C9 and CYP2A6 in human liver microsomes with IC50s of 32.0±3.6 μM and 63.6±4.2 μM, respectively. C-K promotes Aβ clearance by enhancing autophagy via the mTOR signaling pathway in primary astrocytes.

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