CAS 14464-90-5
:2,3-Naphthalenedimethanol,1,2,3,4-tetrahydro-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxy-,(1S,2R,3R)-
Description:
2,3-Naphthalenedimethanol, 1,2,3,4-tetrahydro-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxy-, (1S,2R,3R)-, with CAS number 14464-90-5, is a complex organic compound characterized by its polycyclic structure, which includes a naphthalene core and multiple hydroxyl and methoxy functional groups. This compound exhibits properties typical of polyphenolic compounds, such as antioxidant activity, which may contribute to its potential biological effects. The presence of multiple hydroxyl groups enhances its solubility in polar solvents and may facilitate interactions with biological macromolecules. Additionally, the stereochemistry indicated by the (1S,2R,3R) configuration suggests specific spatial arrangements that could influence its reactivity and interactions in biological systems. Overall, this compound's unique structure and functional groups may make it of interest in various fields, including medicinal chemistry and materials science, although specific applications would depend on further research into its properties and behavior.
Formula:C22H28O8
Synonyms:- 2,3-Naphthalenedimethanol,1,2,3,4-tetrahydro-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxy-,[1S-(1a,2b,3a)]-
- Lyoniresinol
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Found 4 products.
2,3-Naphthalenedimethanol, 1,2,3,4-tetrahydro-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxy-, (1S,2R,3R)-
CAS:Formula:C22H28O8Purity:98.0%Color and Shape:SolidMolecular weight:420.4529Lyoniresinol
CAS:Lyoniresinol, a lignan from Tarenna attenuata, has antioxidant and anti-melanogenic properties, with an IC50 of 82.4 μM; tastes bitter.Formula:C22H28O8Purity:98%Color and Shape:SolidMolecular weight:420.45(+)-Lyoniresinol
CAS:<p>(+)-Lyoniresinol is a natural product with the (R) configuration. It is an enantiomer of (+)-lyoniresinol, which is a phytochemical found in plants such as soybean and cimicifuga foetida. (+)-Lyoniresinol inhibits the growth of bacteria by damaging their cell membranes and inhibiting fatty acid synthesis. This compound also has anti-oxidative effects, which may be due to its ability to inhibit lipid peroxidation. The chemical structure of (+)-Lyoniresinol consists of a benzene ring with two double bonds and one single bond. Preparative high performance liquid chromatography (prep-HPLC) can be used to purify this substance from acetate extract of soybean or cimicifuga foetida.</p>Formula:C22H28O8Purity:Min. 95%Color and Shape:PowderMolecular weight:420.45 g/mol



