- Ginsenoside Rk3
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- $77.00
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2026-07-17
- CAS:364779-15-7
- Purity: 99.33%
- Supply Ability: 10g
- Ginsenoside Rk3
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-
2023-02-24
- CAS:364779-15-7
- Min. Order: 10mg
- Purity: ≥98%(HPLC)
- Supply Ability: 10 g
- Ginsenoside Rk3
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- $1.00
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2019-07-14
- CAS:364779-15-7
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 25kg
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| | Ginsenoside Rk3 Basic information |
| Product Name: | Ginsenoside Rk3 | | Synonyms: | Ginsenoside Rk3;Ginsenoside Rk3 standard;β-D-Glucopyranoside, (3β,6α,12β)-3,12-dihydroxydammara-20,24-dien-6-yl;Ginsenoside Rk3, 10 mM in DMSO | | CAS: | 364779-15-7 | | MF: | C36H60O8 | | MW: | 620.86 | | EINECS: | | | Product Categories: | | | Mol File: | 364779-15-7.mol |  |
| | Ginsenoside Rk3 Chemical Properties |
| Boiling point | 722.4±60.0 °C(Predicted) | | density | 1.20±0.1 g/cm3 (20 ºC 760 Torr) | | storage temp. | 4°C, protect from light | | solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | | form | Powder | | pka | 12.91±0.70(Predicted) | | color | White to off-white |
| | Ginsenoside Rk3 Usage And Synthesis |
| Chemical Properties | White powder, soluble in organic solvents such as methanol, ethanol, and DMSO, derived from ginseng. | | Uses | Ginsenoside Rk3 is isolated from the root of Panax notoginseng which exhibits high inhibitory activity against Epidermophyton floccosum, Trichophyton rubrum, and Trichophyton mentagrophytes. | | in vivo | The inhibitory effects of Ginsenoside Rk3 (Rk3) on tumor progression are studied in vivo using a H460 xenograft model in nude mice. Compared with the control group, a significant inhibition of tumor growth (volume) is observed in the Ginsenoside Rk3-treated group. Twenty-one days after treatment initiation, tumor growth is significantly inhibited by approximately 62.99% in the mice receiving 20 mg/kg Ginsenoside Rk3, similar to the inhibitory effect observed in the 20 mg/kg Gefitinib-treated group (57.21%). Compared with the control group, tumor growth is moderately inhibited in the mice receiving 10 and 5 mg/kg Ginsenoside Rk3, with inhibition rates of 32.54% and 11.84%, respectively[2]. | | IC 50 | NF-κB: 14.24 μM (IC50, in HepG2 cells); NF-κB: 15.32 μM (IC50, in SK-Hep1 cell) |
| | Ginsenoside Rk3 Preparation Products And Raw materials |
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