CAS 118555-84-3
:[1,2'-Bianthracene]-9,9',10,10'-tetrone,1',4,5,8'-tetrahydroxy-2,3'-dimethoxy-6',7-dimethyl-, (1R)- (9CI)
Description:
[1,2'-Bianthracene]-9,9',10,10'-tetrone, 1',4,5,8'-tetrahydroxy-2,3'-dimethoxy-6',7-dimethyl-, (1R)- (9CI) is a complex organic compound characterized by its polycyclic aromatic structure, which includes two anthracene units linked by a tetrone functional group. This compound features multiple hydroxyl (-OH) and methoxy (-OCH3) substituents, contributing to its potential reactivity and solubility properties. The presence of these functional groups suggests that it may exhibit interesting biological activities, possibly acting as an antioxidant or having other pharmacological effects. The stereochemistry indicated by the (1R) designation implies a specific three-dimensional arrangement of atoms, which can influence the compound's interactions with biological targets. Additionally, the compound's CAS number, 118555-84-3, allows for precise identification in chemical databases. Overall, this substance is of interest in fields such as organic chemistry, materials science, and medicinal chemistry due to its unique structural features and potential applications.
Formula:C32H22O10
Synonyms:- [1,2'-Bianthracene]-9,9',10,10'-tetrone,1',4,5,8'-tetrahydroxy-2,3'-dimethoxy-6',7-dimethyl-, (R)-
- 5,7'-Biphyscion
- Floribundone 1
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Found 4 products.
Floribundone 1
CAS:<p>Floribundone 1 is a natural product of Senna, Fabaceae.</p>Formula:C32H22O10Purity:98%Color and Shape:SolidMolecular weight:566.51Floribundone 1
CAS:Formula:C32H22O10Purity:95%~99%Color and Shape:Orange powderMolecular weight:566.518Floribundone 1
CAS:<p>Floribundone 1 is a natural compound isolated from the bark of the genus Populnea. It has shown anti-inflammatory and anti-nociceptive effects in animal models, as well as cancer therapy and chemoprevention. Floribundone 1 inhibits tumor necrosis factor-α (TNF-α), which is a cytokine that plays an important role in inflammation and immune responses. Floribundone 1 also prevents the migration of leukemia cells by blocking their adhesion to endothelial cells in vitro. This compound also inhibits peroxide production, which may be due to its inhibition of phospholipase A2 activity.</p>Formula:C32H22O10Purity:Min. 95%Color and Shape:PowderMolecular weight:566.5 g/mol




