Molecular Formula | C53H86O21 |
Molar Mass | 1059.25 |
Density | 1.43±0.1 g/cm3(Predicted) |
Solubility | Soluble in methanol, ethanol, DMSO and other organic solvents |
Appearance | White crystalline powder |
pKa | 12.50±0.70(Predicted) |
Storage Condition | 2-8℃ |
Physical and Chemical Properties | White crystalline powder, soluble in methanol, ethanol, DMSO and other organic solvents, comes from Acanthopanax senticosus Acanthopanax senticosus dried rhizome. |
In vitro study | Cell Viability Assay Cell Line: RAW264.7 cells Concentration: 10 µM, 20 µM and 40µM Incubation Time: 24 hours Result: Has no effect on cell cytotoxicity and inhibits NO production Western Blot Analysis Cell Line: RAW264.7 cells Concentration: 10 µM, 20 µM and 40µM Incubation Time: 24 hours Result: Decreases p-ERK and p-JNK expression. RT-PCR Cell Line: RAW264.7 cells Concentration: 10 µM, 20 µM and 40µM Incubation Time: 24 hours Result: Decreased COX-2 and iNOS mRNA expression in a dose-dependent manner. |
In vivo study | Animal Model: Mice Dosage: 0.5 mg/kg Administration: Oral administration; 0.5 mg/kg/day; 17 days Result: Reinforced object recognition memory. |
biological activity | Ciwujianoside C3 is an orally active compound that can penetrate the blood-brain barrier, isolated from the leaves of acanthopanax. Ciwujianoside C3 has an anti-inflammatory effect and can enhance the recognition memory of individual mice. |
in vitro study | Cell viabilityassay Cell Line: RAW264.7 cells Concentration: 10 µm, 20 µm and 40 μm invasion Time: 24 hours Result: Has no effect on cell cytotoxicity and intests NO production Western Blot Analysis Cell Line: RAW264.7 cells Concentration: 10 µm, 20 µm and 40 μm Incubation Time: 24 hours Result: Decreases p-ERK and p-JNK expression. RT-PCR Cell Line: RAW264.7 cells Concentration: 10 µM, 20 µM and 40µM Incubation Time: 24 hours Result: Decreased COX-2 and iNOS mRNA expression in a dose-dependent manner. |
Cell Line: | RAW264.7 cells RAW264.7 cells RAW264.7 cells |
Concentration: | 10 µM, 20 µM and 40µM 10 µM, 20 µM and 40µM 10 µM, 20 µM and 40µM |
Incubation Time: | 24 hours 24 hours 24 hours |
Result: | Has no effect on cell cytotoxicity and inhibits NO production Decreases p-ERK and p-JNK expression. Decreased COX-2 and iNOS mRNA expression in a dose-dependent manner. Reinforced object recognition memory. |
in vivo study | Animal Model: Mice Dosage: 0.5 mg/kg Administration: Oral administration; 0.5 mg/kg/day; 17 days Result: informed object recognition memory. |
Animal Model: | Mice |
Dosage: | 0.5 mg/kg |
Administration: | Oral administration; 0.5 mg/kg/day; 17 days |
Chemical properties | white crystalline powder, soluble in methanol, ethanol, DMSO and other organic solvents, dried rhizomes derived from Acanthopanax senticosus. |