Description
Lariciresinol isolated from the herbs of Phyllanthus niruri. Lariciresinol and its 7S,8S,8'R stereoisomer can inhibit the root growth of Italian ryegrass to 51-55% relative to the negative control.
Synonyms
(2S)-2α-(3-Methoxy-4-hydroxyphenyl)-4β-(3-methoxy-4-hydroxybenzyl)tetrahydrofuran-3β-methanol;(2S)-Tetrahydro-2α-(4-hydroxy-3-methoxyphenyl)-4β-[(4-hydroxy-3-methoxyphenyl)methyl]-3β-furanmethanol;2-Methoxy-4-[[(2S)-tetrahydro-2α-(3-methoxy-4-hydroxypheny
IUPAC Name
4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol
Molecular Formula
C20H24O6
Canonical SMILES
COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O
InChI
InChI=1S/C20H24O6/c1-24-18-8-12(3-5-16(18)22)7-14-11-26-20(15(14)10-21)13-4-6-17(23)19(9-13)25-2/h3-6,8-9,14-15,20-23H,7,10-11H2,1-2H3/t14-,15-,20+/m0/s1
InChIKey
MHXCIKYXNYCMHY-AUSJPIAWSA-N
Boiling Point
568.4±50.0 °C(Predicted)
Application
fungicidal activities
Storage
Sealed in dry,Room Temperature
Uses
(+)-Lariciresinol is used in biological studies as an anti-tumor-initiating effects of phenolic compounds isolated from the bark of Picea jezoensis var. jezoensis to evaluate the pharmacological activity.