Ginsenoside CK
- ₹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
1 prices
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)
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
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Signal word: | Warning | ||||||||||||||
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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.More related product prices
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