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| | Esculentic acid Basic information |
| Product Name: | Esculentic acid | | Synonyms: | 2alpha,3alpha,23-trihydroxyurs-12-en-28-oic acid;Esculentic acid;Urs-12-en-28-oic acid,2,3,23-trihydroxy-, (2a,3a,4a)-;Urs-12-en-28-oic acid, 2,3,23-trihydroxy-, (2α,3α,4α)- | | CAS: | 103974-74-9 | | MF: | C30H48O5 | | MW: | 488.71 | | EINECS: | | | Product Categories: | | | Mol File: | 103974-74-9.mol |  |
| | Esculentic acid Chemical Properties |
| Melting point | 270-272 °C | | Boiling point | 609.4±55.0 °C(Predicted) | | density | 1.18±0.1 g/cm3(Predicted) | | solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | | form | Powder | | pka | 4.66±0.70(Predicted) |
| | Esculentic acid Usage And Synthesis |
| Description | Esculentic acid has anti-inflammatory effect.
Esculentic acid has protective effects against LPS-induced endotoxic shock may be mediated, at least in part, by regulation the release of inflammatory cytokines and mediators, and protein expression of COX-2 in mice. | | Definition | ChEBI: 2alpha,3alpha,23-trihydroxyurs-12-en-28-oic acid is a pentacyclic triterpenoid that is urs-12-ene substituted by a carboxy group at position 28 and hydroxy groups at positions 2, 3 and 23 (the 2alpha,3alpha stereoisomer). It has been isolated from Juglans sinensis. It has a role as a plant metabolite. It is a pentacyclic triterpenoid and a hydroxy monocarboxylic acid. It derives from a hydride of an ursane. | | target | COX | TNF-α | IL Receptor |
| | Esculentic acid Preparation Products And Raw materials |
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