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(+)-Epipinoresinol

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(+)-Epipinoresinol Basic information
Product Name:(+)-Epipinoresinol
Synonyms:(+)-Epipinoresinol;(+)-1-epi-Pinoresinol;(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;(1S,3aβ,6aβ)-Tetrahydro-1β,4α-bis(3-methoxy-4-hydroxyphenyl)-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;Phenol, 4,4'-[(1R,3aR,4S,6aR)-tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl]bis[2-methoxy-
CAS:24404-50-0
MF:C20H22O6
MW:358.39
EINECS:
Product Categories:
Mol File:24404-50-0.mol
(+)-Epipinoresinol Structure
(+)-Epipinoresinol Chemical Properties
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form Powder
Boiling point 556.5±50.0 °C(Predicted)
density 1.287±0.06 g/cm3(Predicted)
Melting point 137-138 °C
pKa9.54±0.35(Predicted)
color White to off-white
Safety Information
MSDS Information
(+)-Epipinoresinol Usage And Synthesis
Uses(+)-Epipinoresinol is a lignan compound. CYP81Q3 specifically catalyzes methylenedioxy bridge (MDB) formation in (+)-Epipinoresinol to produce (+)-Pluviatilol[1].
DefinitionChEBI: 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
(+)-Epipinoresinol Preparation Products And Raw materials
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