(Q27121534)

4,4'-tetrahydro-1h,3h-furo[3,4-c]furan-1,4-diylbis(2,6-dimethoxyphenol) (English)

6 October 2016

chemical formula

C₂₂H₂₆O₈

1 reference

4,4'-tetrahydro-1h,3h-furo[3,4-c]furan-1,4-diylbis(2,6-dimethoxyphenol) (English)

6 October 2016

canonical SMILES

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

1 reference

Non-Alkaloidal Constituents from the Stem ofFicus Septica

4,4'-tetrahydro-1h,3h-furo[3,4-c]furan-1,4-diylbis(2,6-dimethoxyphenol) (English)

6 October 2016

1 reference

Aspidosperma marcgravianum

1 reference

Alkaloid studies—LVIII: The alkaloids of six Aspidosperma species

Eleutherococcus sessiliflorus

1 reference

Enantioselective induction of SIRT1 gene by syringaresinol from Panax ginseng berry and Acanthopanax senticosus Harms stem.

Syringa vulgaris

5 references

Syringaresinol induces mitochondrial biogenesis through activation of PPARβ pathway in skeletal muscle cells

Neuritogenesis of herbal ( )- and (-)-syringaresinols separated by chiral HPLC in PC12h and Neuro2a cells

Syringaresinol causes vasorelaxation by elevating nitric oxide production through the phosphorylation and dimerization of endothelial nitric oxide synthase

Enantioselective induction of SIRT1 gene by syringaresinol from Panax ginseng berry and Acanthopanax senticosus Harms stem.

Modulation of gut microbiota and delayed immunosenescence as a result of syringaresinol consumption in middle-aged mice

Chrysanthemum indicum

1 reference

Chemical constituents from flowers of Chrysanthemum indicum

Actinidia chinensis

1 reference

Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry

asparagus

1 reference

Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry

Avena sativa

1 reference

Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry

Cucumis sativus

1 reference

Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry

Fagopyrum esculentum

1 reference

Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry

Fragaria

1 reference

Content, composition, and stereochemical characterisation of lignans in berries and seeds

Hordeum vulgare

1 reference

Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry

Linum usitatissimum

1 reference

Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry

Raphanus sativus var. sativus

1 reference

Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry

Ribes nigrum

1 reference

Content, composition, and stereochemical characterisation of lignans in berries and seeds

Rubus chamaemorus

1 reference

Content, composition, and stereochemical characterisation of lignans in berries and seeds

Secale cereale

1 reference

Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry

Solanum melongena

1 reference

Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry

Triticum aestivum

1 reference

Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry

Vaccinium myrtillus

1 reference

Content, composition, and stereochemical characterisation of lignans in berries and seeds

Vaccinium vitis-idaea

1 reference

Content, composition, and stereochemical characterisation of lignans in berries and seeds

Vitis vinifera

1 reference

Lignans in selected wines

Garcia

1 reference

Triterpenes from Garcia parviflora. Cytotoxic evaluation of natural and semisynthetic friedelanes.

Machilus zuihoensis

1 reference

Bioactive neolignans and lignans from the bark of Machilus robusta

Machilus odoratissima

1 reference

Bioactive neolignans and lignans from the bark of Machilus robusta

Sarcopyramis nepalensis

1 reference

Structural elucidation of a new flavone fromSarcopyramis nepalensis

Cinnamomum osmophloeum

1 reference

Cytotoxic lignan esters from Cinnamomum osmophloeum

Casearia membranacea

1 reference

A cytotoxic butenolide, two new dolabellane diterpenoids, a chroman and a benzoquinol derivative formosan Casearia membranacea

Drypetes littoralis

1 reference

Chemical constituents from Drypetes littoralis

Dendrobium longicornu

1 reference

Five new compounds from Dendrobium longicornu

Wikstroemia lanceolata

1 reference

New lignans and cytotoxic constituents from Wikstroemia lanceolata

Daphne tangutica

1 reference

Chemical constituents investigation of Daphne tangutica.

Papaver canescens

1 reference

Quaternary Alkaloids of Papaver spicatum

Artabotrys

1 reference

New constituents from stems of Artabotrys uncinatus

Codonopsis pilosula

1 reference

New Constituents from Codonopsis pilosula

Diospyros eriantha

1 reference

Antibacterial activity of diosquinone isolated from Diospyros tricolor

Zanthoxylum integrifoliolum

1 reference

New phenylpropenoids, bis(1-phenylethyl)phenols, bisquinolinone alkaloid, and anti-inflammatory constituents from Zanthoxylum integrifoliolum

Trigonostemon

1 reference

A new cytotoxic daphnane diterpenoid, rediocide G, from Trigonostemon reidioides

Annona senegalensis

1 reference

Antiplatelet aggregation constituents from Annona purpurea

Curcuma aeruginosa

1 reference

Sesquiterpenes from the rhizomes of Curcuma heyneana

Saussurea costus

1 reference

Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of Saussureosides A and B from Saussurea medusa

Artemisia carvifolia

2 references

Cytotoxic terpenoids and flavonoids from Artemisia annua

Chemical constituents from the aerial parts of Artemisia minor.

Artemisia apiacea

2 references

Cytotoxic terpenoids and flavonoids from Artemisia annua

Chemical constituents from the aerial parts of Artemisia minor.

Neolitsea pulchella

1 reference

Cytotoxic constituents of the stem bark of Neolitsea acuminatissima

Saussurea pulchella

1 reference

Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of Saussureosides A and B from Saussurea medusa

Annona emarginata

1 reference

Antiplatelet aggregation constituents from Annona purpurea

Tarenna

1 reference

Mixed lignan-neolignans from Tarenna attenuata

Sophora leachiana

1 reference

A new pterocarpan, (-)-maackiain sulfate, from the roots of Sophora subprostrata

Artemisia caucasica

2 references

Cytotoxic terpenoids and flavonoids from Artemisia annua

Chemical constituents from the aerial parts of Artemisia minor.

Phyllanthus virgatus

1 reference

Novel sesquiterpenoids from the roots of Phyllanthus emblica

Phyllanthus oligospermus

1 reference

Novel sesquiterpenoids from the roots of Phyllanthus emblica

Cassytha

1 reference

Chemical constituents from Cassytha filiformis II

Juniperus scopulorum

1 reference

Antiplatelet and vasorelaxing actions of the acetoxy derivative of cedranediol isolated from Juniperus squamata

Selaginella

1 reference

Phenolic Constituents of Selaginella doederleinii

Artemisia pectinata

2 references

Cytotoxic terpenoids and flavonoids from Artemisia annua

Chemical constituents from the aerial parts of Artemisia minor.

Asclepias subulata

1 reference

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

Gnetum

1 reference

Stilbene derivatives from Gnetum gnemon Linn.

Gaeumannomyces

1 reference

Antimalarial compounds from Rhaphidophora decursiva

Rhaphidophora

1 reference

Antimalarial compounds from Rhaphidophora decursiva

Polla

1 reference

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

Vismia guianensis

1 reference

Xanthones, xanthonolignoids and other constituents of the roots of vismia guaramirangae

Talipariti tiliaceum

1 reference

Constituents from the stems of Hibiscus taiwanensis.

Piper eucalyptifolium

2 references

Constituents from Piper divaricatum

Bioactive lignans from Peperomia duclouxii

Machilus odoratissimus

1 reference

Bioactive neolignans and lignans from the bark of Machilus robusta

Papaver pseudocanescens

1 reference

Quaternary Alkaloids of Papaver spicatum

Artemisia caruifolia

2 references

Chemical constituents from the aerial parts of Artemisia minor.

Cytotoxic terpenoids and flavonoids from Artemisia annua

Machilus thunbergii

1 reference

Bioactive neolignans and lignans from the bark of Machilus robusta

Cinnamomum reticulatum

1 reference

Isolation of new esters from the stems of Cinnamomum reticulatum Hay.

Eleutherococcus senticosus

1 reference

A new 3,4-seco-lupane-type triterpenoid from the pulp of Acanthopanax senticosus (Rupr. et Maxim) Harms

Annona cherimola

1 reference

Antiplatelet aggregation constituents from Annona purpurea

Hibiscus cannabinus

1 reference

Constituents from the stems of Hibiscus taiwanensis.

Cinnamomum subavenium

1 reference

Cytotoxic compounds from the stems of Cinnamomum tenuifolium.

Dendrobium nobile

1 reference

Antifibrotic Phenanthrenes ofDendrobium nobileStems

Artemisia minor

1 reference

Cytotoxic terpenoids and flavonoids from Artemisia annua

Hibiscus syriacus

1 reference

Constituents from the stems of Hibiscus taiwanensis.

Annona montana

1 reference

Antiplatelet aggregation constituents from Annona purpurea

Viburnum foetidum var. foetidum

1 reference

Four new lignans from Viburnum foetidum var. foedidum

Lilium auratum

1 reference

Lipid and steroidal constituents of Lilium auratum var. Platyphyllum AND L. tenuifolium

Viscum album

1 reference

Viscum album (mistletoe)

Magnolia grandiflora

1 reference

Two new germacranolides from Magnolia grandiflora

Dracaena draco

1 reference

Icogenin, a New Cytotoxic Steroidal Saponin Isolated from Dracaena draco.

Neopallasia pectinata

2 references

Chemical constituents from the aerial parts of Artemisia minor.

Cytotoxic terpenoids and flavonoids from Artemisia annua

Artemisia alpina

2 references

Chemical constituents from the aerial parts of Artemisia minor.

Cytotoxic terpenoids and flavonoids from Artemisia annua

Aspidosperma excelsum

1 reference

Alkaloid studies—LVIII: The alkaloids of six Aspidosperma species

tomato

1 reference

Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry

Hornstedtia reticulata

1 reference

Isolation of new esters from the stems of Cinnamomum reticulatum Hay.

Identifiers

InChI

InChI=1S/C22H26O8/c1-25-15-5-11(6-16(26-2)19(15)23)21-13-9-30-22(14(13)10-29-21)12-7-17(27-3)20(24)18(8-12)28-4/h5-8,13-14,21-24H,9-10H2,1-4H3

1 reference

4,4'-tetrahydro-1h,3h-furo[3,4-c]furan-1,4-diylbis(2,6-dimethoxyphenol) (English)

6 October 2016

2 references

4,4'-tetrahydro-1h,3h-furo[3,4-c]furan-1,4-diylbis(2,6-dimethoxyphenol) (English)

6 October 2016

ChEBI release 2020-09-01

1 reference

4,4'-Tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diylbis(2,6-dimethoxyphenol) (English)

6 October 2016

2 references

4,4'-tetrahydro-1h,3h-furo[3,4-c]furan-1,4-diylbis(2,6-dimethoxyphenol) (English)

6 October 2016

ChEBI ID

49211

mapping relation type

2 references

syringaresinol (English)

6 October 2016

International Chemical Identifier

InChI

InChI=1S/C22H26O8/c1-25-15-5-11(6-16(26-2)19(15)23)21-13-9-30-22(14(13)10-29-21)12-7-17(27-3)20(24)18(8-12)28-4/h5-8,13-14,21-24H,9-10H2,1-4H3

SureChEMBL ID

SCHEMBL120485

2 references

based on heuristic

inferred from InChIKey

Human Metabolome Database ID

1 reference

HMDB0038928

2 references

based on heuristic

inferred from InChIKey

KNApSAcK ID

C00053808

2 references

based on heuristic

inferred from InChIKey