8-Hydroxypinoresinol (Q104959632)

3,6-Bis(4-hydroxy-3-methoxyphenyl)-3,4,6,6a-tetrahydro-1H-furo[3,4-c]furan-3a-ol

inferred from SMILES

1 reference

inferred from SMILES

mass

374.136553044 dalton

1 reference

1H,3H-Furo[3,4-c]furan-3a(4H)-ol, dihydro-1,4-bis(4-hydroxy-3-methoxyphenyl)-, (1R,3aS,4S,6aR)-

inferred from SMILES

stereoisomer of

1 reference

(3R,3aS,6R,6aR)-3,6-bis(4-hydroxy-3-methoxyphenyl)-3,4,6,6a-tetrahydro-1H-furo[3,4-c]furan-3a-ol

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₂₀H₂₂O₇

0 references

canonical SMILES

OC1=CC=C(C=C1OC)C2OCC3(O)C(OCC23)C4=CC=C(O)C(OC)=C4

0 references

isomeric SMILES

COc1cc([C@H]2OC[C@]3(O)[C@@H](c4ccc(O)c(OC)c4)OC[C@H]23)ccc1O

0 references

found in taxon

Valeriana prionophylla

1 reference

New lignans from the roots of Valeriana prionophylla with antioxidative and vasorelaxant activities.

Carduus vivariensis

1 reference

Lignans and flavonoids from Carduus assoi

Echinacea purpurea

1 reference

Structure and accumulation of phenolics in elicited Echinacea purpurea cell cultures

Eucommia ulmoides

1 reference

The constituents of Eucommia ulmoides Oliv. V. Isolation of dihydroxydehydrodiconiferyl alcohol isomers and phenolic compounds.

Fraxinus japonica

1 reference

Lignans from bark of Fraxinus mandshurica var. japonica and F. japonica

Fraxinus mandschurica

1 reference

Lignans from bark of Fraxinus mandshurica var. japonica and F. japonica

Olea europaea

1 reference

Lignans from bark of the Olea plants. I

Schisandra lancifolia

1 reference

Chemical constituents from the leaves and stems of Schisandra lancifolia

Strophanthus gratus

1 reference

Lignans from Strophanthus gratus

Valeriana laxiflora

1 reference

Antitubercular constituents of Valeriana laxiflora

Valeriana microphylla

1 reference

Valtrates and Lignans in Valeriana microphylla

Valeriana officinalis

1 reference

Sesquiterpenoids and lignans from the roots of Valeriana officinalis L

Fraxinus chinensis

1 reference

Lignans from bark of Fraxinus mandshurica var. japonica and F. japonica

Schisandra sphenanthera

1 reference

Lignans from Schisandra sphenathera Rehd. et Wils. and semisynthetic schisantherin A analogues: absolute configuration, and their estrogenic and anti-proliferative activity.

Forsythia suspensa

1 reference

Characterization of phenolic compounds in the fruits of Forsythia suspensa by high-performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry.

Fraxinus longicuspis

1 reference

Lignans from bark of Fraxinus mandshurica var. japonica and F. japonica

Carduus nigrescens

1 reference

Lignans and flavonoids from Carduus assoi

Tectona grandis

1 reference

Tectonoelins, new norlignans from a bioactive extract of Tectona grandis

Identifiers

InChI

InChI=1S/C20H22O7/c1-24-16-7-11(3-5-14(16)21)18-13-9-26-19(20(13,23)10-27-18)12-4-6-15(22)17(8-12)25-2/h3-8,13,18-19,21-23H,9-10H2,1-2H3/t13-,18-,19-,20-/m1/s1

0 references

0 references

CAS Registry Number

81426-17-7

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

2 references

17 September 2022

inferred from InChIKey

ChEBI ID

175806

mapping relation type

exact match

2 references

ChEBI release 2022-06-13

International Chemical Identifier

InChI

InChI=1S/C20H22O7/c1-24-16-7-11(3-5-14(16)21)18-13-9-26-19(20(13,23)10-27-18)12-4-6-15(22)17(8-12)25-2/h3-8,13,18-19,21-23H,9-10H2,1-2H3/t13-,18-,19-,20-/m1/s1

1 reference

1 reference

Human Metabolome Database ID

HMDB0033279

2 references

inferred from InChIKey