(Q83048126)

inferred from SMILES

mass

520.194461844 dalton

1 reference

(3R,4S)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-[[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl]oxolan-2-one

inferred from SMILES

stereoisomer of

2 references

(3S,4S)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-[[3-methoxy-4-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl]oxolan-2-one

inferred from InChIKey

1 reference

1 reference

inferred from InChI

chemical formula

C₂₆H₃₂O₁₁

0 references

canonical SMILES

O=C1OCC(CC2=CC=C(O)C(OC)=C2)C1CC3=CC=C(OC4OC(CO)C(O)C(O)C4O)C(OC)=C3

0 references

isomeric SMILES

COC1=C(C=CC(=C1)C[C@H]2COC(=O)[C@@H]2CC3=CC(=C(C=C3)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)OC)O

0 references

found in taxon

Forsythia viridissima

2 references

Phenolic compounds from Forsythia leaves

Production of cornoside in Abeliophyllum distichum cell suspension cultures

Forsythia koreana

2 references

Phenolic compounds from Forsythia leaves

Production of cornoside in Abeliophyllum distichum cell suspension cultures

Daphne feddei

1 reference

Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production

Symplocos caudata

1 reference

Neolignan glycosides from Symplocos caudata

Symplocos sumuntia

1 reference

Neolignan glycosides from Symplocos caudata

Abeliophyllum distichum

1 reference

Production of cornoside in Abeliophyllum distichum cell suspension cultures

Centaurea nigra

1 reference

Dibenzylbutyrolactone lignans and indole alkaloids from the seeds of Centaurea nigra (Asteraceae)

Centaurea scabiosa

2 references

Centaurea scabiosa: a source of dibenzylbutyrolactone lignans

Biological Activity of Lignans from the Seeds of Centaurea scabiosa

Centaurea urvillei

1 reference

Bioactivity of two Turkish endemic Centaurea species, and their major constituents

Forsythia ovata

1 reference

Phenolic compounds from Forsythia leaves. II.

Saussurea parviflora

1 reference

Eudesmane derivatives and other constituents from Saussurea parviflora

Trachelospermum axillare

1 reference

Lignans from Trachelospermum axillare

Trachelospermum gracilipes

1 reference

Lignan diglucosides from Trachelospermum asiaticum

Saussurea salicifolia

1 reference

The chemopreventive effects of Saussurea salicifolia through induction of apoptosis and phase II detoxification enzyme.

Symplocos setchuensis

1 reference

Anti-AIDS agents. 46. Anti-HIV activity of harman, an anti-HIV principle from Symplocos setchuensis, and its derivatives

Forsythia suspensa

1 reference

Characterization of phenolic compounds in the fruits of Forsythia suspensa by high-performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry.

Psephellus schischkinii

1 reference

Isolation, structure elucidation and bioactivity of schischkiniin, a unique indole alkaloid from the seeds of Centaurea schischkinii

Centaurea sclerolepis

1 reference

Guaianolides from the Aerial Parts of Centaurea Hololeuca

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

Styrax japonicus

1 reference

Matrix metalloproteinase-1 inhibitor from the stem bark of Styrax japonica S. et Z.

Centaurea raphanina

1 reference

Bioactivity of two Turkish endemic Centaurea species, and their major constituents

Symplocos theifolia

1 reference

Anti-AIDS agents. 46. Anti-HIV activity of harman, an anti-HIV principle from Symplocos setchuensis, and its derivatives

Trachelospermum asiaticum

1 reference

Lignan diglucosides from Trachelospermum asiaticum

Centaurea melitensis

2 references

Lignan glucosides from the seeds of Centaurea americana (Compositae)

Americanin, a bioactive dibenzylbutyrolactone lignan, from the seeds of Centaurea americana

Identifiers

InChI

InChI=1S/C26H32O11/c1-33-19-9-13(3-5-17(19)28)7-15-12-35-25(32)16(15)8-14-4-6-18(20(10-14)34-2)36-26-24(31)23(30)22(29)21(11-27)37-26/h3-6,9-10,15-16,21-24,26-31H,7-8,11-12H2,1-2H3/t15-,16+,21+,22+,23-,24+,26+/m0/s1

0 references

0 references

CAS Registry Number

23202-85-9

1 reference

https://commonchemistry.cas.org/detail?cas_rn=23202-85-9

10 April 2021

PubChem CID

486612

1 reference

ChEBI ID

132820

mapping relation type

exact match

2 references

ChEBI release 2021-03-01

International Chemical Identifier

InChI

InChI=1S/C26H32O11/c1-33-19-9-13(3-5-17(19)28)7-15-12-35-25(32)16(15)8-14-4-6-18(20(10-14)34-2)36-26-24(31)23(30)22(29)21(11-27)37-26/h3-6,9-10,15-16,21-24,26-31H,7-8,11-12H2,1-2H3/t15-,16+,21+,22+,23-,24+,26+/m0/s1

1 reference

1 reference

DSSTOX compound identifier

DTXCID40100275

0 references

UNII

XRE59W9FDD

1 reference