| Name | curculigoside |
|---|---|
| Synonyms |
β-D-Glucopyranoside, 2-(((2,6-dimethoxybenzoyl)oxy)methyl)-4-hydroxyphenyl
Curculigoside A 2-(β-D-Glucopyranosyloxy)-5-hydroxybenzyl 2,6-dimethoxybenzoate Benzoic acid, 2,6-dimethoxy-, [2-(β-D-glucopyranosyloxy)-5-hydroxyphenyl]methyl ester |
| Description | Curculigoside is the main saponin in C. orchioide, exerts significant antioxidant, anti-osteoporosis, antidepressant and neuroprotection effects. Curculigoside possesses significant anti-arthritic effects in vivo and in vitro via regulation of the JAK/STAT/NF-κB signaling pathway[1]. |
|---|---|
| Related Catalog | |
| Target |
JAK; STAT; NF-κB[1] |
| In Vitro | Curculigoside (1-64 μg/ml; 72 hours) exerts significant inhibitory effects on MH7A cell viability between 1 and 64 µg/ml in MH7A cells[1]. Curculigoside (4-16 μg/ml; 24 hours) decreases the protein expression of JAK1, JAK3 and STAT3 compared to the TNF-α group[1]. Cell Viability Assay[1] Cell Line: MH7A cells Concentration: 1 μg/ml; 2 μg/ml; 4 μg/ml; 8 μg/ml; 16 μg/ml; 32 μg/ml; 64 μg/ml Incubation Time: 72 hours Result: Had inhibitory effect on MH7A cells. Western Blot Analysis[1] Cell Line: MH7A cells Concentration: 4 μg/ml; 64 μg/ml Incubation Time: 24 hours Result: Downregulated JAK1, JAK3 and STAT3 protein expression. |
| References |
| Density | 1.5±0.1 g/cm3 |
|---|---|
| Boiling Point | 734.9±60.0 °C at 760 mmHg |
| Melting Point | 158-160ºC |
| Molecular Formula | C22H26O11 |
| Molecular Weight | 466.435 |
| Flash Point | 253.8±26.4 °C |
| Exact Mass | 466.147522 |
| PSA | 164.37000 |
| LogP | -0.02 |
| Vapour Pressure | 0.0±2.5 mmHg at 25°C |
| Index of Refraction | 1.624 |
| Safety Phrases | 24/25 |
|---|---|
| HS Code | 29389090 |