CAS 868168-04-1

Indeno[1',2':2,3]indeno[5,4-b]furan-5,8,10-triol, 1-(3,5-dihydroxyphenyl)-1,2,6,6a,11,11a-hexahydro-2,6,11-tris(4-hydroxyphenyl)-, (1R,2R,6R,6aR,11R,11aR)-rel-(+)-

Description:

Indeno[1',2':2,3]indeno[5,4-b]furan-5,8,10-triol, with the CAS number 868168-04-1, is a complex organic compound characterized by its polycyclic structure, which includes multiple fused aromatic rings and hydroxyl functional groups. This compound exhibits significant structural complexity, featuring a unique arrangement of indeno and furan moieties, which contributes to its potential biological activity. The presence of multiple hydroxyl groups suggests that it may engage in hydrogen bonding, influencing its solubility and reactivity. Additionally, the stereochemistry indicated by the (1R,2R,6R,6aR,11R,11aR)-rel-(+)- designation implies that the compound has specific spatial arrangements that could affect its interactions with biological targets. Such characteristics may render it of interest in medicinal chemistry, particularly in the development of therapeutic agents. Its intricate structure and functional groups may also provide avenues for further chemical modifications, enhancing its potential applications in various fields, including pharmaceuticals and materials science.

Formula: C₄₂H₃₂O₉

Synonyms:

• Indeno[1',2':2,3]indeno[5,4-b]furan-5,8,10-triol, 1-(3,5-dihydroxyphenyl)-1,2,6,6a,11,11a-hexahydro-2,6,11-tris(4-hydroxyphenyl)-, (1R,2R,6R,6aR,11R,11aR)-rel-(+)-
• Carasiphenol C

Carasiphenol C

CAS: 868168-04-1

Carasiphenol C is a natural product from Carex humilis Leyss.

Formula: C₄₂H₃₂O₉

Purity: 98%

Color and Shape: Solid

Molecular weight: 680.7

Ref: TM-TN3593

Carasiphenol C

CAS: 868168-04-1

Carasiphenol C is a synthetic analog of resveratrol, which is a stilbenoid compound known for its potential health benefits. This compound is often derived from chemical synthesis processes that modify the natural resveratrol structure to enhance its bioactivity and stability. The mode of action of Carasiphenol C involves modulating various signaling pathways associated with oxidative stress and inflammation, including the inhibition of NF-kB and activation of the SIRT1 pathway. This activity makes it a potential candidate for research into therapeutic applications for chronic inflammatory conditions and diseases associated with oxidative damage.

Formula: C₄₂H₃₂O₉

Purity: Min. 95%

Molecular weight: 680.70 g/mol

Ref: 3D-TJB16804