ChemicalBook--->CAS DataBase List--->40957-99-1

40957-99-1

40957-99-1 Structure

40957-99-1 Structure
IdentificationBack Directory
[Name]

Medioresil
[CAS]

40957-99-1
[Synonyms]

Medioresil
Medioresinol
(+)-Medioresinol
Medioresil ISO 9001:2015 REACH
4-[(1S,3aR,4S,6aR)-4-(4-Hydroxy-3-methoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan-1-yl]-2,6-dimethoxyphenol
Phenol,2,6-dimethoxy-4-[(1S,3aR,4S,6aR)- tetrahydro-4-(4-hydroxy-3-methoxyphenyl)- 1H,3H-furo[3,4-c]furan-1-yl]-
4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol
[Molecular Formula]

C21H24O7
[MDL Number]

MFCD20275045
[MOL File]

40957-99-1.mol
[Molecular Weight]

388.41
Chemical PropertiesBack Directory
[Melting point ]

170-172 °C(Solv: methanol (67-56-1))
[Boiling point ]

575.7±50.0 °C(Predicted)
[density ]

1.284±0.06 g/cm3(Predicted)
[storage temp. ]

4°C, protect from light
[form ]

Solid
[pka]

9.84±0.35(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

(+)-Medioresinol is a furofuran type lignan with antifungal, antibacterial and lesishmanicidal activities. (+)-Medioresinol leads to intracellular ROS accumulation and mitochondria-mediated apoptotic cell death in Candida albicans. (+)-Medioresinol can reduce the cardiovascular disease risk[1][2].
[Definition]

ChEBI: (-)-medioresinol is a lignan that is tetrahydro-1H,3H-furo[3,4-c]furan substituted by a 4-hydroxy-3,5-dimethoxyphenyl group at position 1 and a 4-hydroxy-3-methoxyphenyl group at position 4. It has been isolated from the stems of Sinocalamus affinis. It has a role as a plant metabolite. It is a lignan, a dimethoxybenzene, a furofuran and a polyphenol.
[References]

[1] Ji Hong Hwang, et al. (+)-Medioresinol leads to intracellular ROS accumulation and mitochondria-mediated apoptotic cell death in Candida albicans. Biochimie. 2012 Aug;94(8):1784-93. DOI:10.1016/j.biochi.2012.04.010
[2] Ji Hong Hwang, et al. Synergistic antibacterial and antibiofilm effect between (+)-medioresinol and antibiotics in vitro. Appl Biochem Biotechnol. 2013 Aug;170(8):1934-41. DOI:10.1007/s12010-013-0351-7
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