| Identification | Back Directory | [Name]
Lanosta-7,25-dien-18-oic acid, 20-hydroxy-3-[(O-3-O-methyl-β-D-glucopyranosyl-(1→3)-O-β-D-glucopyranosyl-(1→4)-O-[β-D-xylopyranosyl-(1→2)]-O-6-deoxy-β-D-glucopyranosyl-(1→2)-4-O-sulfo-β-D-xylopyranosyl)oxy]-16-oxo-, γ-lactone, sodium salt (1:1), (3β)- | [CAS]
95499-80-2 | [Synonyms]
Cucumarioside A2-2
Lanosta-7,25-dien-18-oic acid, 20-hydroxy-3-[(O-3-O-methyl-β-D-glucopyranosyl-(1→3)-O-β-D-glucopyranosyl-(1→4)-O-[β-D-xylopyranosyl-(1→2)]-O-6-deoxy-β-D-glucopyranosyl-(1→2)-4-O-sulfo-β-D-xylopyranosyl)oxy]-16-oxo-, γ-lactone, sodium salt (1:1), (3β)- | [Molecular Formula]
C59H93NaO29S | [MOL File]
95499-80-2.mol | [Molecular Weight]
1321.41 |
| Hazard Information | Back Directory | [Description]
Cucumarioside A2-2 is a triterpene glycoside. Cucumarioside A2-2 is isolated from the Far-Eastern sea cucumber Cucumaria japonica. Cucumarioside A2-2 exhibits antitumor activity. | [Uses]
Cucumarioside A2-2 is a triterpene glycoside with antitumor activity. Cucumarioside A2-2 can induce mouse macrophage polarization toward the M1 phenotype. Cucumarioside A2-2 pretreated macrophages can effectively and selectively target and kill multiple types of cancer cells. Cucumarioside A2-2-induced M1 macrophages can effectively target and penetrate tumor tissues and improve the survival rate of mice in an allogeneic model. Exogenous activation of Cucumarioside A2-2 provides a useful model for the subsequent development of antitumor cell immunosuppression[1]. | [References]
[1] Holothurian triterpene glycoside cucumarioside A2-2 induces macrophages activation and polarization in cancer immunotherapy DOI:10.1186/s12935-023-03141-z |
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