| Identification | Back Directory | [Name]
(+)-Epipinoresinol | [CAS]
24404-50-0 | [Synonyms]
(+)-Epipinoresinol
(+)-1-epi-Pinoresinol
(1S,3aβ,6aβ)-Tetrahydro-1β,4α-bis(3-methoxy-4-hydroxyphenyl)-1H,3H-furo[3,4-c]furan
Phenol, 4,4'-[(1R,3aR,4S,6aR)-tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl]bis[2-methoxy-
(1R)-1α,4β-Bis(4-hydroxy-3-methoxyphenyl)-3aβ,4,6,6aβ-tetrahydro-1H,3H-furo[3,4-c]furan
(1S)-1β,4α-Bis(3-methoxy-4-hydroxyphenyl)-3aβ,4,6,6aβ-tetrahydro-1H,3H-furo[3,4-c]furan
2-Methoxy-4-[[(3S)-6β-(3-methoxy-4-hydroxyphenyl)-3aα,4,6,6aα-tetrahydro-1H,3H-furo[3,4-c]furan]-3α-yl]phenol | [Molecular Formula]
C20H22O6 | [MDL Number]
MFCD11111283 | [MOL File]
24404-50-0.mol | [Molecular Weight]
358.39 |
| Chemical Properties | Back Directory | [solubility ]
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | [Boiling point ]
556.5±50.0 °C(Predicted) | [density ]
1.287±0.06 g/cm3(Predicted) | [form ]
Powder | [Melting point ]
137-138 °C | [pka]
9.54±0.35(Predicted) | [color ]
White to off-white |
| Hazard Information | Back Directory | [Uses]
(+)-Epipinoresinol is a lignan compound. CYP81Q3 specifically catalyzes methylenedioxy bridge (MDB) formation in (+)-Epipinoresinol to produce (+)-Pluviatilol[1]. | [Definition]
ChEBI: Epipinoresinol is an enantiomer of pinoresinol having (+)-(1R,3aR,4S,6aR)-configuration. It has a role as a plant metabolite and a marine metabolite. | [References]
[1] Eiichiro Ono, et al. Formation of a Methylenedioxy Bridge in (+)-Epipinoresinol by CYP81Q3 Corroborates with Diastereomeric Specialization in Sesame Lignans. Plant Cell Physiol. 2018 Nov 1;59(11):2278-2287. DOI:10.1093/pcp/pcy150 |
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