(Q27105196)

inferred from InChIKey

mass

386.173±0 dalton

1 reference

( )-Eudesmin (English)

(3S,3aS,6S,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan

5 October 2016

stereoisomer of

1 reference

inferred from InChIKey

Diaeudesmin

1 reference

(3R,3aS,6R,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan

inferred from InChI

1 reference

1 reference

1 reference

C₂₂H₂₆O₆

1 reference

( )-Eudesmin (English)

5 October 2016

canonical SMILES

COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC

1 reference

( )-Eudesmin (English)

5 October 2016

isomeric SMILES

COC1=C(C=C(C=C1)[C@@H]2[C@H]3CO[C@@H]([C@H]3CO2)C4=CC(=C(C=C4)OC)OC)OC

1 reference

Lignoids and arylalkanones from fruits of Virola elongata

( )-Eudesmin (English)

5 October 2016

1 reference

Zanthoxylum heitzii

1 reference

Oxidative burst inhibitory and cytotoxic amides and lignans from the stem bark of Fagara heitzii (Rutaceae).

Raulinoa echinata

1 reference

Separation and NMR studies on lignans of Raulinoa echinata

Machilus wangchiana

1 reference

Chemical constituents of the bark of Machilus wangchiana and their biological activities

Magnolia biondii

5 references

Lignans with platelet activating factor antagonist activity from magnolia biondii

A neolignan and lignans from Magnolia biondii

On the Ca -antagonistic principles of the flower buds of Magnolia fargesii

Lignans with platelet activating factor antagonist activity from magnolia biondii

Two new stereoisomers of Tetrahydrofuranoid lignans from the flower buds of Magnolia fargesii

Pandanus odoratissimus

2 references

Antioxidative Activities of constituents Isolated from Pandanus odoratissimus

Antioxidative Activities of constituents Isolated from Pandanus odoratissimus

Lindera praecox

2 references

Insect Antifeeding Substances inParabenzoin praecoxandPiper futokadzura

A lignan from Lindera praecox

Araucaria angustifolia

2 references

Phenylpropanoid derivatives and biflavones at different stages of differentiation and development of Araucaria angustifolia.

Phenylpropanoid derivatives and biflavones at different stages of differentiation and development of Araucaria angustifolia.

Aristolochia pubescens

1 reference

2,3-Dihydrobenzofuran neolignans from Aristolochia pubescens

Laurelia novae-zelandiae

1 reference

Phytochemical Investigation of Laurelia novae-zelandiae

Licaria armeniaca

1 reference

Neolignans from the fruits of Licaria armeniaca

Magnolia denudata

1 reference

Chemical constituents from the leaves of Magnolia denudata

Magnolia kobus

4 references

Formation of ( )-eudesmin in Magnolia kobus DC. Var. borealis sarg

Lignans from the Bark ofMagnolia kobus

Furofuran lignans from the bark of Magnolia kobus

Lignans and sesquiterpenes from Magnolia praecocissima

Magnolia × soulangeana

1 reference

Lignans in flower buds of Magnolia saulangiana

Melicope hayesii

2 references

Lignans and coumarins metabolites from Melicopehayesii

Lignans and coumarins metabolites from Melicopehayesii

Annona mucosa

1 reference

Tryptamine derived amides and acetogenins from the seeds of Rollinia mucosa

Rudbeckia maxima

1 reference

Sesquiterpene lactones and lignanes from Rudbeckia species

Rudbeckia nitida

1 reference

Sesquiterpene lactones and lignanes from Rudbeckia species

Rudbeckia scabrifolia

1 reference

Sesquiterpene lactones and lignanes from Rudbeckia species

Virola michelii

1 reference

Constituents from the leaves of Aquilaria sinensis

Zanthoxylum fagara

1 reference

Lignans and Other Constituents from South and Central AmericanZanthoxylumSpecies

Aglaia abbreviata

1 reference

Aglaianine, a new bisamide from Aglaia abbreviata

Aglaia elaeagnoidea

1 reference

Aglaianine, a new bisamide from Aglaia abbreviata

Daphne oleoides

1 reference

Terpenoids and aromatic compounds from Daphne oleoides ssp. oleoides

Haplophyllum acutifolium

2 references

Accelerated dereplication of crude extracts using HPLC-PDA-MS-SPE-NMR: quinolinone alkaloids of Haplophyllum acutifolium

Alkaloids ofHaplophyllum perforatum

Magnolia praecocissima

1 reference

Lignans and sesquiterpenes from Magnolia praecocissima

Metrodorea flavida

1 reference

Coumarins from Metrodorea flavida

Samadera bidwillii

1 reference

The secondary metabolites of aff. Samadera SAC-2825: An australian simaroubaceae with unusual chemistry

Zanthoxylum simulans

1 reference

Two dimeric lignans with an unusual α,β-unsaturated ketone motif from Zanthoxylum podocarpum and their inhibitory effects on nitric oxide production

Pandanus tectorius

1 reference

Antioxidative Activities of constituents Isolated from Pandanus odoratissimus

Pandanus odorifer

1 reference

Antioxidative Activities of constituents Isolated from Pandanus odoratissimus

Propolis

2 references

Cytotoxic constituents from Brazilian red propolis and their structure-activity relationship.

Constituents of Brazilian red propolis and their preferential cytotoxic activity against human pancreatic PANC-1 cancer cell line in nutrient-deprived condition.

Identifiers

InChI

InChI=1S/C22H26O6/c1-23-17-7-5-13(9-19(17)25-3)21-15-11-28-22(16(15)12-27-21)14-6-8-18(24-2)20(10-14)26-4/h5-10,15-16,21-22H,11-12H2,1-4H3/t15-,16-,21 ,22 /m0/s1

1 reference

( )-Eudesmin (English)

5 October 2016

2 references

( )-Eudesmin (English)

5 October 2016

ChEBI release 2020-09-01

2 references

( )-Eudesmin (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=29106-36-3

9 April 2021

1 reference

(7S,7’S,8R,8’R)-eudesmin (English)

5 October 2016

2 references

( )-Eudesmin (English)

5 October 2016

ChEBI ID

23

mapping relation type

2 references

( )-Eudesmin (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C22H26O6/c1-23-17-7-5-13(9-19(17)25-3)21-15-11-28-22(16(15)12-27-21)14-6-8-18(24-2)20(10-14)26-4/h5-10,15-16,21-22H,11-12H2,1-4H3/t15-,16-,21 ,22 /m0/s1

1 reference

MSBNK-RIKEN_NPDepo-CB000323

( )-EUDESMIN (English)

5 October 2016

1 reference

MassBank accession ID

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

MSBNK-RIKEN_NPDepo-NGA01689

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

MSBNK-RIKEN_NPDepo-NGA01690

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

MSBNK-RIKEN_NPDepo-NGA01691

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

MSBNK-RIKEN_NPDepo-NGA01692

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

splash10-0udi-0920000000-15b37331f1c4c530d9e2

0 references

DSSTox substance ID

DTXSID50951699

1 reference

DSSTOX compound identifier

DTXCID001379810

0 references

KNApSAcK ID

C00000640

reason for deprecated rank

cannot be confirmed by other sources

1 reference

( )-Eudesmin (English)

5 October 2016

UNII

3TPV0HJ9B0

1 reference

0 references

1 reference

( )-Eudesmin (English)