(Q105303103)

inferred from SMILES

mass

580.215591212 dalton

1 reference

(2S,3R,4S,5S,6R)-2-[4-[(3R,3aR,6S,6aR)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

inferred from SMILES

stereoisomer of

2 references

(2R,3R,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

2 references

(2R,3S,4R,5R,6S)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

(+)-syringaresinol beta-D-glucoside

1 reference

(2S,3R,4S,5R,6S)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

1 reference

(2S,3R,4S,5S,6R)-2-[4-[(3S,3aS,6S,6aS)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

Eleutherococcus senticosus

chemical formula

C₂₈H₃₆O₁₃

0 references

canonical SMILES

OC1=C(OC)C=C(C=C1OC)C2OCC3C(OCC23)C4=CC(OC)=C(OC5OC(CO)C(O)C(O)C5O)C(OC)=C4

0 references

isomeric SMILES

COc1cc([C@@H]2OC[C@@H]3[C@H]2CO[C@H]3c2cc(OC)c(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c(OC)c2)cc(OC)c1O

0 references

found in taxon

1 reference

Eleutherococcus senticosus (Siberian Ginseng)

Daphne feddei

2 references

Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production

Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production

Albizia julibrissin

1 reference

Studies on leguminous plants. Part XXVI. Lignoids from Albizziae Cortex. II. A Biodegradation Pathway of Syringaresinol.

Aster auriculatus

1 reference

Lignan and acetylenic glycosides from Aster auriculatus

Senna alexandrina

1 reference

An anthraquinone glycoside fromCassia angustifolia leaves

Dalbergia sissoo

1 reference

Constituents of Dalbergia sissoo Roxb. leaves with osteogenic activity.

Dendrobium moniliforme

1 reference

Copacamphane, picrotoxane, and alloaromadendrane sesquiterpene glycosides and phenolic glycosides from Dendrobium moniliforme

Diospyros kaki

1 reference

A new 18,19-secoursane triterpene from the leaves of Diospyros kaki

Ginkgo biloba

1 reference

Biologically active secondary metabolites from Ginkgo biloba

Globularia alypum

1 reference

Phenylethyl Glycosides fromGlobularia alypumGrowing in Turkey

Leontodon tuberosus

1 reference

A New Eudesmane Derivative from Leontodon tuberosus

Magnolia coco

1 reference

The Constituents from the Leaves ofMagnolia coco

Magnolia officinalis

1 reference

Isolation and Characterization of Phenolic Compounds from Magnoliae Cortex Produced in China.

Pedicularis densispica

1 reference

Chemical Constituents of Pedicularis densispica Franch

Ipomoea nil

1 reference

Bioactive phenolic constituents from the seeds of Pharbitis nil.

Phlogacanthus curviflorus

1 reference

Diterpenes and Diterpene Glucosides fromPhlogacanthus curviflorus

Salacia chinensis

1 reference

Chemical structures and hepatoprotective effects of constituents from the leaves of Salacia chinensis

Taraxacum udum

1 reference

Sesquiterpenoids and phenolics from roots of Taraxacum udum.

Youngia japonica

1 reference

Studies on the constituents of whole plants of Youngia japonica.

Thrincia tuberosa

1 reference

A New Eudesmane Derivative from Leontodon tuberosus

Identifiers

InChI

InChI=1S/C28H36O13/c1-34-16-5-12(6-17(35-2)21(16)30)25-14-10-39-26(15(14)11-38-25)13-7-18(36-3)27(19(8-13)37-4)41-28-24(33)23(32)22(31)20(9-29)40-28/h5-8,14-15,20,22-26,28-33H,9-11H2,1-4H3/t14-,15-,20-,22-,23+,24-,25+,26+,28+/m1/s1

0 references

InChIKey

WEKCEGQSIIQPAQ-FKLBZQFOSA-N

0 references

1 reference

17 September 2022

1 reference

1 reference