(Q27136115)

MEDIORESINOL (English)

4-[(3R,3aS,6R,6aS)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol

7 October 2016

stereoisomer of

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₂₁H₂₄O₇

1 reference

MEDIORESINOL (English)

7 October 2016

canonical SMILES

COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC

1 reference

MEDIORESINOL (English)

7 October 2016

isomeric SMILES

COC1=CC(=CC(=C1O)OC)[C@@H]2[C@H]3CO[C@@H]([C@H]3CO2)C4=CC(=C(C=C4)O)OC

1 reference

Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production

MEDIORESINOL (English)

7 October 2016

1 reference

Doliocarpus dentatus

1 reference

Isolation of leishmanicidal triterpenes and lignans from the Amazonian liana Doliocarpus dentatus (dilleniaceae)

Eucommia ulmoides

3 references

The constituents of Eucommia ulmoides OLIV. II. Isolation and structures of three new lignan glycosides.

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

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

Piper cubeba

3 references

Potent CYP3A4 inhibitory constituents of Piper cubeba

Potent CYP3A4 inhibitory constituents of Piper cubeba

Potent CYP3A4 Inhibitory Constituents of Piper cubeba

Rubia wallichiana

4 references

Cytotoxic anthraquinones from the stems of Rubia wallichiana Decne

Cytotoxic anthraquinones from the stems of Rubia wallichiana Decne

Cytotoxic anthraquinones from the stems of Rubia wallichiana Decne

Cytotoxic Anthraquinones from the Stems of Rubia wallichiana Decne

Allamanda schottii

1 reference

9α-hydroxypinoresinol, 9α-hydroxymedioresinol and related lignans from Allamanda neriifolia

Aralia bipinnata

1 reference

Lignans from the wood of Aralia bipinnata

Aristolochia elegans

2 references

The alkaloids and other constituents from the root and stem of Aristolochia elegans

The alkaloids and other constituents from the root and stem of Aristolochia elegans

Hedyotis lawsoniae

2 references

Studies on the constituents of medicinal and related plants in Sri Lanka. III. Novel sesquilignans from Hedyotis lawsoniae.

Studies on the constituents of medicinal and related plants in Sri Lanka. III. Novel sesquilignans from Hedyotis lawsoniae.

Justicia diffusa

2 references

Lignans from Justicia hyssopifolia

Justicia lignans VI--prostalidin D, a new arylnaphthalide lignan from Justicia diffusa var. prostrata C.B. Clarke

Justicia glauca

1 reference

Justiciresinol, a New Furanoid Lignan from Justicia glauca

Magnolia grandiflora

1 reference

Melampolides from Magnolia grandiflora

Sambucus nigra

2 references

Potential allelochemicals from Sambucus nigra

Potential allelochemicals from Sambucus nigra

Saussurea medusa

2 references

Immunosuppressive constituents from Saussurea medusa

Immunosuppressive constituents from Saussurea medusa

Tripterygium wilfordii

1 reference

Chemical Constituents from the Root of Tripterygium wilfordii

Aconitum kongboense

1 reference

Chemical constituents of the aerial parts of Aconitum kongboense

Asclepias curassavica

1 reference

New cardenolide and acylated lignan glycosides from the aerial parts of Asclepias curassavica

Catunaregam spinosa

1 reference

ChemInform Abstract: Minor Compounds from the Stem Bark of Chinese Mangrove Associate Catunaregam spinosa

Dirca occidentalis

1 reference

Plant anticancer agents XXVII: Antileukemic and cytotoxic constituents of Dirca occidentalis (Thymelaeaceae).

Gnetum montanum

1 reference

Lignans from Gnetum montanum Markgr. f. megalocarpua

common sunflower

1 reference

Bioactive lignans from a cultivar of Helianthus annuus

Peperomia heyneana

1 reference

Bioactive lignans from Peperomia duclouxii

Rhaphidophora decursiva

1 reference

Antimalarial compounds from Rhaphidophora decursiva

Wikstroemia hainanensis

1 reference

Lignans fromWikstroemia hainanensis

Spatholobus suberectus

1 reference

Chemical constituents of Spatholobus suberectus

Bupleurum salicifolium

1 reference

Salicifoliol, a New Furolactone-Type Lignan from Bupleurum salicifolium

Ophryosporus lorentzii

1 reference

Chromanones, benzofurans and other constituents from Ophryosporus lorentzii

Hibiscus cannabinus

1 reference

Phenolic constituents from the core of kenaf (Hibiscus cannabinus).

Saccharum officinarum

1 reference

Antioxidative Compounds Isolated from Kokuto, Non-centrifugal Cane Sugar

pomegranate

1 reference

Diverse Phytochemicals and Bioactivities in the Ancient Fruit and Modern Functional Food Pomegranate (Punica granatum).

Justicia tranquebariensis

1 reference

Justica tranquebariensis Linn. f.

Rosmarinus officinalis

1 reference

Phytochemical Profiling of Flavonoids, Phenolic Acids, Terpenoids, and Volatile Fraction of a Rosemary (Rosmarinus officinalis L.) Extract.

Bambusa emeiensis

1 reference

Lignans and neolignans from Sinocalamus affinis and their absolute configurations.

Aristolochia littoralis

1 reference

The alkaloids and other constituents from the root and stem of Aristolochia elegans

Brucea javanica

1 reference

Chemical constituents from Brucea javanica

Actinidia arguta

2 references

Flavan-3-ols having a gamma-lactam from the roots of Actinidia arguta inhibit the formation of advanced glycation end products in vitro

Lilac alcohol epoxide: a linalool derivative in Actinidia arguta flowers.

Identifiers

InChI

InChI=1S/C21H24O7/c1-24-16-6-11(4-5-15(16)22)20-13-9-28-21(14(13)10-27-20)12-7-17(25-2)19(23)18(8-12)26-3/h4-8,13-14,20-23H,9-10H2,1-3H3/t13-,14-,20 ,21 /m0/s1

1 reference

MEDIORESINOL (English)

7 October 2016

2 references

MEDIORESINOL (English)

7 October 2016

ChEBI release 2020-09-01

CAS Registry Number

40957-99-1

1 reference

https://commonchemistry.cas.org/detail?cas_rn=40957-99-1

9 April 2021

1 reference

4-[(1S,3aR,4S,6aR)-4-(4-Hydroxy-3-methoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan-1-yl]-2,6-dimethoxyphenol (English)

7 October 2016

2 references

MEDIORESINOL (English)

7 October 2016

Reaxys registry number

4569869

1 reference

(-)-medioresinol (English)

7 October 2016

ChEBI ID

67644

mapping relation type

2 references

(-)-medioresinol (English)

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C21H24O7/c1-24-16-6-11(4-5-15(16)22)20-13-9-28-21(14(13)10-27-20)12-7-17(25-2)19(23)18(8-12)26-3/h4-8,13-14,20-23H,9-10H2,1-3H3/t13-,14-,20 ,21 /m0/s1

1 reference

CHEMBL376507 (English)

7 October 2016

1 reference

1 reference

DSSTOX compound identifier

DTXCID301389165

0 references

UNII

J74JLA8FFA

1 reference