|   Sodium Aescinate structure | Common Name | Sodium Aescinate | ||
|---|---|---|---|---|
| CAS Number | 20977-05-3 | Molecular Weight | 1124.2202 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C54H83NaO23 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
| Use of Sodium AescinateSodium aescinate is a triterpene saponin derived from Aesculus hippocastanum seeds, with anti-inflammatory and antioxidant activities[1]. Sodium aescinate inhibits hepatocellular carcinoma growth by targeting CARMA3/NF-κB pathway[2]. | 
| Name | Escin monosodium salt | 
|---|---|
| Synonym | More Synonyms | 
| Description | Sodium aescinate is a triterpene saponin derived from Aesculus hippocastanum seeds, with anti-inflammatory and antioxidant activities[1]. Sodium aescinate inhibits hepatocellular carcinoma growth by targeting CARMA3/NF-κB pathway[2]. | 
|---|---|
| Related Catalog | |
| In Vitro | Sodium aescinate can block signals transiting to downstream molecules AKT, ERK, inhibit the proliferation of breast cancer cell MCF-7 cell apoptosis and induced cell apoptosis by suppressing the activation of SRC[3]. | 
| In Vivo | Sodium aescinate may effectively controls and improves wound healing in diabetic rats via its anti-inflammatory and antioxidant activities[1]. Sodium aescinate treatment can alleviate the symptom of polycystic ovary syndrome (PCOS) in rat model through regulating the PI3K/Akt/GSK3-β pathway[4]. | 
| References | 
| Molecular Formula | C54H83NaO23 | 
|---|---|
| Molecular Weight | 1124.2202 | 
| 3-methyl-pyridine-2-carbonitrile | 
| 3-methyl-2-pyridinecarbonitrile | 
| 2-cyano-3-methly pyridine | 
| 2-cyano-b-picoline | 
| 3-methylpyridine-2-carbonitrile | 
| 2-Cyano-3-methylpyridine | 
| (h4tes4)[qr] | 
| akrochem tdec | 
| diethyl-carbamodithioicacitetrakis(anhydrosulfide)withthiotelluricac | 
| Sodium escinate |