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ChemicalBook--->CAS DataBase List--->548-29-8

548-29-8

548-29-8 Structure

548-29-8 Structure
IdentificationBack Directory
[Name]

(+)-ISOLARICIRESINOL
[CAS]

548-29-8
[Synonyms]

Isolariciresil
ISOLARICIRESINOL
Cyclolariciresinol
(+)-Isolariciresinol
-Conidendryl alcohol
(+)-ISOLARICIRESINOL
Isolariciresinol (6CI)
(6R,7R,8S)-isolariciresinol
(7S,8R,8'R)-(+)-Cyclolariciresinol
(2R,3R,4S)-4-(4-hydroxy-3-methoxy-phenyl)-7-methoxy-2,3-dimethylol-tetralin-6-ol
(2R)-4β-(4-Hydroxy-3-methoxyphenyl)-6-hydroxy-7-methoxy-1,2,3,4-tetrahydronaphthalene-2β,3α-dimethanol
(1S)-1,2,3,4-Tetrahydro-7-hydroxy-1α-(4-hydroxy-3-methoxyphenyl)-6-methoxy-2β,3α-naphthalenedimethanol
(1S)-1α-(3-Methoxy-4-hydroxyphenyl)-6-methoxy-7-hydroxy-1,2,3,4-tetrahydronaphthalene-2β,3α-bismethanol
(1S,2R,3R)-1,2,3,4-Tetrahydro-7-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-6-methoxy-2,3-naphthalenedimethanol
2,3-Naphthalenedimethanol,1,2,3,4-tetrahydro-7-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-6-methoxy-,(1S,2R,3R)-
(6R,7R,8S)-8-(4-hydroxy-3-methoxyphenyl)-6,7-bis(hydroxymethyl)-3-methoxy-5,6,7,8-tetrahydronaphthalen-2-ol
(6R,7R,8S)-8-(4-hydroxy-3-methoxy-phenyl)-6,7-bis(hydroxymethyl)-3-methoxy-5,6,7,8-tetrahydronaphthalen-2-ol
[Molecular Formula]

C20H24O6
[MDL Number]

MFCD07784475
[MOL File]

548-29-8.mol
[Molecular Weight]

360.4
Chemical PropertiesBack Directory
[Melting point ]

112 °C
[Boiling point ]

584.1±50.0 °C(Predicted)
[density ]

1.275±0.06 g/cm3(Predicted)
[storage temp. ]

-20°C
[solubility ]

Acetone: soluble,Chloroform: soluble,Dichloromethane: soluble,DMSO: soluble,Ethyl Acetate: soluble
[form ]

Powder
[pka]

10.08±0.35(Predicted)
[color ]

White to off-white
[LogP]

1.640 (est)
Hazard InformationBack Directory
[Uses]

Cyclolariciresinol can be used to reduce oxidative stress and inflammation by activating farnesoid x receptor in cholestatis by alpha-naphthylisothiocyanate.
[Definition]

ChEBI: (+)-isolariciresinol is a lignan that is 5,6,7,8-tetrahydronaphthalen-2-ol substituted by hydroxymethyl groups at positions 6 and 7, a methoxy group at position 3 and a 4-hydroxy-3-methoxyphenyl group at position 8. It has been isolated from the roots of Rubia yunnanensis. It has a role as a plant metabolite. It is a lignan, a polyphenol, a primary alcohol and a member of guaiacols.
[target]

Immunology & Inflammation related
[storage]

-20°C
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