| Name | α-CHACONINE |
|---|---|
| Synonyms |
chaconine
chaconine,a a-chaconine with tlc a-chaconine a-chaconine from potato sprouts alpa-chaconine |
| Description | α-Chaconine, isolated from a Solanum tuberosum L. cv Jayoung, inhibits the expressions of COX-2, IL-1β, IL-6, and TNF-α at the transcriptional level. α-Chaconine inhibits the LPS-induced expressions of iNOS and COX-2 at the protein and mRNA levels and their promoter activities in RAW 264.7 macrophages. Anti-inflammatory effects[1]. |
|---|---|
| Related Catalog | |
| Target |
COX-2 |
| In Vitro | α-Chaconine attenuates the transcriptional activity of activator protein-1 (AP-1) by reducing the translocation and phosphorylation of c-Jun.α-Chaconine suppresses lipopolysaccharide-induced pro-inflammatory mediators via AP-1 inactivation in RAW 264.7 macrophages and protects mice from endotoxin shock.α-Chaconine also suppresses the phosphorylation of TGF-β-activated kinase-1 (TAK1), which lies upstream of MKK7/JNK signaling[1]. |
| References |
| Density | 1.37 g/cm3 |
|---|---|
| Melting Point | 228-236ºC |
| Molecular Formula | C45H73NO14 |
| Molecular Weight | 852.05900 |
| Exact Mass | 851.50300 |
| PSA | 220.46000 |
| LogP | 1.12070 |
| Index of Refraction | 1.621 |
| Water Solubility | pyridine: 10 mg/mL, clear, very faintly yellow |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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| Hazard Codes | Xn: Harmful; |
|---|---|
| Risk Phrases | R63 |
| Safety Phrases | 22-36/37 |
| RIDADR | UN 1544 |
| WGK Germany | 3 |
| RTECS | FL6700000 |
| Packaging Group | III |
| Hazard Class | 6.1(b) |