Chemical Structure : Ginsenoside compound K
CAS No.: 39262-14-1
Catalog No.: PC-28727Not For Human Use, Lab Use Only.
Ginsenoside compound K (GCK, Ginsenoside C-K, Ginsenoside K) is a deglycosylated ginsenoside metabolite with anti-inflammatory, vascular-protective and anticancer properties, targets DUSP5 to inhibit the malignant progression of glioblastoma, also inhibits PRELID3B (Kd=23 uM) to inhibit lung cancer.
| Packing | Price | Stock | Quantity |
|---|---|---|---|
| 25 mg | $78 | In stock | |
| 50 mg | $118 | In stock | |
| 100 mg | $178 | In stock | |
| 250 mg | Get quote |
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Ginsenoside compound K (GCK, Ginsenoside C-K, Ginsenoside K) is a deglycosylated ginsenoside metabolite with anti-inflammatory, vascular-protective and anticancer properties, targets DUSP5 to inhibit the malignant progression of glioblastoma, also inhibits PRELID3B (Kd=23 uM) to inhibit lung cancer.
Ginsenoside compound K (GCK, Ginsenoside C-K) inhibits complement C1qA/C3-CR3-mediated microglial synaptic pruning and neuronal pyroptosis.
Ginsenoside compound K (GCK, Ginsenoside C-K) inhibits and stabilizes PRELID3B in cellular thermal shift assay and bind PRELID3B with Kd of 23 uM.
Ginsenoside compound K (GCK, Ginsenoside C-K) markedly inhibited the proliferation and migration of glioblastoma cells and significantly disrupted their cell cycle.
Ginsenoside compound K (GCK, Ginsenoside C-K) suppresses glioblastoma progression by dephosphorylating p-ERK1/2 via upregulation of DUSP5 expression.
Ginsenoside compound K (GCK, Ginsenoside C-K) exerts osteoprotective effects by suppressing osteoclastogenesis and promoting preosteoclast PDGF-BB-induced angiogenesis via targeting CSF1R.
Ginsenoside compound K (GCK, Ginsenoside C-K) exhibits anti-inflammatory effects by reducing iNOS and COX-2. suppresses cancerous cell proliferation, and the safeguarding of cardiovascular, hepatic, and renal functions.
| M.Wt | 622.88 | |
| Formula | C36H62O8 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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| Chemical Name/SMILES |
(2S,3R,4S,5S,6R)-2-(((S)-2-((3S,5R,8R,9R,10R,12R,13R,14R,17S)-3,12-Dihydroxy-4,4,8,10,14-pentamethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-methylhept-5-en-2-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol |
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1. He J, et al. Proc Natl Acad Sci U S A. 2026 May 12;123(19):e2533505123.
2. Zhao X, et al. J Ethnopharmacol. 2026 Oct 18;374(Pt 3):122537.
3. Tang F, et al. Eur J Pharmacol. 2026 Mar 28;1019:178678.

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