(Q27136660)

(+)-lyoniresinol (English)

(6R,7S,8S)-8-(4-hydroxy-3,5-dimethoxyphenyl)-6,7-bis(hydroxymethyl)-1,3-dimethoxy-5,6,7,8-tetrahydronaphthalen-2-ol

7 October 2016

stereoisomer of

1 reference

(7R,8R,7'R)-(+)-Lyoniresinol

inferred from InChIKey

2 references

inferred from InChIKey

(6S,7R,8S)-8-(4-hydroxy-3,5-dimethoxyphenyl)-6,7-bis(hydroxymethyl)-1,3-dimethoxy-5,6,7,8-tetrahydronaphthalen-2-ol

inferred from InChI

2 references

inferred from InChIKey

1 reference

1 reference

C₂₂H₂₈O₈

1 reference

(+)-lyoniresinol (English)

7 October 2016

canonical SMILES

COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO

1 reference

(+)-lyoniresinol (English)

7 October 2016

isomeric SMILES

COC1=CC(=CC(=C1O)OC)[C@@H]2[C@H]([C@@H](CC3=CC(=C(C(=C23)OC)O)OC)CO)CO

1 reference

Tyrosinase inhibitory lignans from the methanol extract of the roots of Vitex negundo Linn. and their structure-activity relationship

(+)-lyoniresinol (English)

7 October 2016

1 reference

Berberis vulgaris

1 reference

Antioxidant and cytoprotective compounds from Berberis vulgaris (barberry).

Combretum quadrangulare

1 reference

Hepatoprotective constituents of the seeds of Combretum quadrangulare

Cotylelobium melanoxylon

2 references

Antidiabetogenic constituents from the Thai traditional medicine Cotylelobium melanoxylon.

Antidiabetogenic constituents from the Thai traditional medicine Cotylelobium melanoxylon.

Hopea utilis

1 reference

Hopeafuran and a C-glucosyl resveratrol isolated from stem wood of Hopea utilis

Phyllostachys edulis

2 references

Two lignan dimers from bamboo stems (Phyllostachys edulis)

Two lignan dimers from bamboo stems (Phyllostachys edulis)

Salacia chinensis

5 references

Structures of new friedelane-type triterpenes and eudesmane-type sesquiterpene and aldose reductase inhibitors from Salacia chinensis

Structures of new friedelane- and norfriedelane-type triterpenes and polyacylated eudesmane-type sesquiterpene from Salacia chinensis LINN. (S. prinoides DC., Hippocrateaceae) and radical scavenging activities of principal constituents

Structures of new friedelane-type triterpenes and eudesmane-type sesquiterpene and aldose reductase inhibitors from Salacia chinensis

Structures of new friedelane-type triterpenes and eudesmane-type sesquiterpene and aldose reductase inhibitors from Salacia chinensis

Structures of New Friedelane- and Norfriedelane-Type Triterpenes and Polyacylated Eudesmane-Type Sesquiterpene from Salacia chinensis Linn. (S. prinoides DC., Hippocrateaceae) and Radical Scavenging Activities of Principal Constituents.

Tabernaemontana cymosa

1 reference

Alkaloids and other compounds from seeds of Tabernaemontana cymosa

Zanthoxylum piperitum

1 reference

Chemical Study of Indonesian Medicinal Plants

Berberis koreana

2 references

Biological evaluation of phenolic constituents from the trunk of Berberis koreana

Biological evaluation of phenolic constituents from the trunk of Berberis koreana

Machilus robusta

1 reference

Bioactive neolignans and lignans from the bark of Machilus robusta

Acer truncatum

1 reference

A new neolignan glycoside from the leaves of Acer truncatum.

Alangium premnifolium

1 reference

Lignan and neolignan glycosides from stems of Alangium premnifolium

Avicennia marina

1 reference

New abietane diterpenoids from the mangrove Avicennia marina

Santalum album

1 reference

Aromatic constituents from the heartwood of Santalum album L

Bambusa emeiensis

1 reference

Lignans and neolignans from Sinocalamus affinis and their absolute configurations.

Biancaea sappan

1 reference

A new 3-benzylchroman derivative from Sappan Lignum (Caesalpinia sappan).

Mespilodaphne cymbarum

1 reference

Allylphenols from Ocotea cymbarum

Quercus petraea

1 reference

Lignan Glycosides from the Heartwood of European Oak Quercus petraea

Litsea coreana

1 reference

Constituents from the stems of Actinodaphne lancifolia

Identifiers

InChI

InChI=1S/C22H28O8/c1-27-15-7-12(8-16(28-2)20(15)25)18-14(10-24)13(9-23)5-11-6-17(29-3)21(26)22(30-4)19(11)18/h6-8,13-14,18,23-26H,5,9-10H2,1-4H3/t13-,14-,18+/m0/s1

1 reference

(+)-lyoniresinol (English)

ZDVZKBOFCHOPLM-SUNYJGFJSA-N

7 October 2016

InChIKey

2 references

(+)-lyoniresinol (English)

7 October 2016

ChEBI release 2020-09-01

1 reference

(+)-lyoniresinol (English)

7 October 2016

2 references

(+)-lyoniresinol (English)

matched by identifier from

7 October 2016

InChIKey

ZDVZKBOFCHOPLM-SUNYJGFJSA-N

Reaxys registry number

2191984

1 reference

(+)-lyoniresinol (English)

7 October 2016

ChEBI ID

68168

mapping relation type

2 references

(+)-lyoniresinol (English)

matched by identifier from

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C22H28O8/c1-27-15-7-12(8-16(28-2)20(15)25)18-14(10-24)13(9-23)5-11-6-17(29-3)21(26)22(30-4)19(11)18/h6-8,13-14,18,23-26H,5,9-10H2,1-4H3/t13-,14-,18+/m0/s1

1 reference