(Q104402857)

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

inferred from SMILES

1 reference

inferred from SMILES

mass

520.194461844 dalton

1 reference

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

inferred from SMILES

stereoisomer of

2 references

inferred from InChIKey

Epipinoresinol 4'-O-glucoside

2 references

inferred from InChIKey

2-Methoxy-4-[(1S,3abeta,6abeta)-tetrahydro-4beta-[3-methoxy-4-(alpha-D-galactopyranosyloxy)phenyl]-1H,3H-furo[3,4-c]furan-1beta-yl]phenol

1 reference

(-)-Pinoresinol glucoside

1 reference

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

1 reference

chemical formula

C₂₆H₃₂O₁₁

0 references

canonical SMILES

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

0 references

isomeric SMILES

COc1cc([C@H]2OC[C@@H]3[C@@H](c4ccc(O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O)c(OC)c4)OC[C@H]23)ccc1O

0 references

found in taxon

Festuca argentina

1 reference

Lignans and a stilbene from Festuca argentina

Allamanda schottii

1 reference

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

Capparis flavicans

1 reference

Antiestrogenic constituents of the Thai medicinal plants Capparis flavicans and Vitex glabrata

Syringa reticulata

2 references

Secoiridoid glucosides and related compounds from Syringa reticulata and their antioxidant activities

Secoiridoid glucosides and related compounds from Syringa reticulata and their antioxidant activities

Abies nephrolepis

1 reference

Phenolic compounds of Abies nephrolepis and their NO production inhibitory activities.

Epimedium sagittatum

1 reference

Lignan and terpene glycosides from Epimedium sagittatum

Angelica tenuisecta var. furcijuga

1 reference

Medicinal foodstuffs. XX. Vasorelaxant active constituents from the roots of Angelica furcijuga Kitagawa: structures of hyuganins A, B, C, and D

Arnica mollis

1 reference

A 1,5-cis-guaianolide glucoside from flowers of Arnica mollis

Baccharis dracunculifolia

1 reference

Studies on the constituents from the aerial part of Baccharis dracunculifolia DC. II.

Balanophora japonica

1 reference

Balanophonin, a new neo-lignan from Balanophora japonica Makino.

Carex distachya

1 reference

Potential food additives from Carex distachya roots: identification and in vitro antioxidant properties

Centaurea montana

1 reference

Montamine, a unique dimeric indole alkaloid, from the seeds of Centaurea montana (Asteraceae), and its in vitro cytotoxic activity against the CaCo2 colon cancer cells

Cistanche tubulosa

3 references

Iridoid and acyclic monoterpene glycosides, kankanosides L, M, N, O, and P from Cistanche tubulosa.

Phenylethanoid oligoglycosides and acylated oligosugars with vasorelaxant activity from Cistanche tubulosa

The constituents of Cistanche tubulosa (Schrenk) Hook. f. II. Isolation and structures of a new phenylethanoid glycoside and a new neolignan glycoside.

Daphne acutiloba

1 reference

Two biflavonoids from Daphne acutiloba

Forsythia europaea

1 reference

Phenolic compounds from Forsythia leaves. II.

Forsythia giraldiana

1 reference

Phenolic compounds from Forsythia leaves. II.

Forsythia japonica

1 reference

Phenolic compounds from Forsythia leaves. II.

Forsythia koreana

1 reference

A Phenylethanoid Glycoside and Other Constituents from the Fruits of Forsythia koreana

Macaranga tanarius

1 reference

Absolute configuration of (+)-pinoresinol 4-O-[6''-O-galloyl]-beta-D-glucopyranoside, macarangiosides E, and F isolated from the leaves of Macaranga tanarius

Narthecium asiaticum

1 reference

Structures of toxic steroidal saponins from Narthecium asiaticum MAXIM

Pinus massoniana

1 reference

The Constituents of Conifer Needles. Dilignol Glycosides from Pinus massoniana Lamb.

Prunus domestica

1 reference

Abscisic acid related compounds and lignans in prunes (Prunus domestica L.) and their oxygen radical absorbance capacity (ORAC).

Rubus amabilis

1 reference

Pregnane glycoside, lignan glycosides, triterpene glycosyl ester and flavonoid glycosides from Rubus amabilis

Saussurea medusa

1 reference

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

sesame

1 reference

New lignans from the perisperm of Sesamum indicum

Strychnos axillaris

1 reference

Phenolic and iridoid glycosides from Strychnos axillaris

Tinospora sinensis

1 reference

New lignan glucosides from the stems of Tinospora sinensis

Cistanche phelypaea

3 references

Phenylethanoid oligoglycosides and acylated oligosugars with vasorelaxant activity from Cistanche tubulosa

Iridoid and acyclic monoterpene glycosides, kankanosides L, M, N, O, and P from Cistanche tubulosa.

The constituents of Cistanche tubulosa (Schrenk) Hook. f. II. Isolation and structures of a new phenylethanoid glycoside and a new neolignan glycoside.

Identifiers

InChI

InChI=1S/C26H32O11/c1-32-18-7-12(3-5-16(18)28)24-14-10-35-25(15(14)11-34-24)13-4-6-17(19(8-13)33-2)36-26-23(31)22(30)21(29)20(9-27)37-26/h3-8,14-15,20-31H,9-11H2,1-2H3/t14-,15-,20+,21+,22-,23+,24+,25+,26+/m0/s1

0 references

InChIKey

QLJNETOQFQXTLI-WMYFGKAISA-N

0 references

1 reference

17 September 2022

inferred from InChIKey

ChEBI ID

188731

mapping relation type

exact match

1 reference