Forsythin (Q27151384)

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

Phillyrin (English)

8 October 2016

2 references

based on heuristic

inferred from InChIKey

1 reference

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

1 reference

1 reference

C₂₇H₃₄O₁₁

1 reference

Phillyrin (English)

8 October 2016

COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)OC

1 reference

Phillyrin (English)

8 October 2016

COC1=C(C=C(C=C1)[C@H]2[C@H]3CO[C@@H]([C@H]3CO2)C4=CC(=C(C=C4)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)OC)OC

1 reference

Phillyrin (English)

8 October 2016

Anisacanthus virgularis

1 reference

The First Report on the Occurrence of Furofuranoid Lignan Glucosides in Acanthaceae

Bupleurum wenchuanense

2 references

Lignan glucosides from Bupleurum wenchuanense

Saikosaponin derivatives from Bupleurum wenchuanense

Eremophila racemosa

1 reference

Serrulatane diterpenes from Eremophila spp.

Forsythia europaea

2 references

Forsythia giraldiana

2 references

Forsythia japonica

2 references

Forsythia koreana

2 references

Phenolic compounds from Forsythia leaves

Studies on the Methods for Chemical Identification of Forsythiae Fructus and Plantaginis Herba

Forsythia suspensa

8 references

A new lignan glycoside from Forsythia suspensa

Anti-emetic principles of Inula linariaefolia flowers and Forsythia suspensa fruits

Phenolic compounds from Forsythia leaves

Studies on the Methods for Chemical Identification of Forsythiae Fructus and Plantaginis Herba

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

Forsythia suspensa extract alleviates hypersensitivity induced by soybean beta-conglycinin in weaned piglets

Lignans from the fruits of Forsythia suspensa

Antioxidant and antibacterial activity of two compounds (forsythiaside and forsythin) isolated from Forsythia suspensa

Lancea tibetica

1 reference

Lignan and phenylpropanoid glycosides from Lancea tibetica and their antitumor activity

Osmanthus × fortunei

1 reference

Studies on the Constituents of Osmanthus Species. IV. On the Components of the Leaves of Osmanthus fortunei CARR.

Osmanthus fragrans

1 reference

Studies on the Constituents of Osmanthus Species. I. On the Components of the Leaves of Osmanthus fragrans LOUR. var. aurantiacus MAKINO (1)

Phillyrea latifolia

3 references

Lignan and phenylpropanoid glycosides from Phillyrea latifolia and their in vitro anti-inflammatory activity

Phytochemical analysis of Phillyrea latifolia L., a new source of oleuropeoside

Lignan and phenylpropanoid glycosides from Phillyrea latifolia and their in vitro anti-inflammatory activity

Anisacanthus quadrifidus

1 reference

The First Report on the Occurrence of Furofuranoid Lignan Glucosides in Acanthaceae

Forsythia viridissima

1 reference

Studies on the Methods for Chemical Identification of Forsythiae Fructus and Plantaginis Herba

Identifiers

InChI

InChI=1S/C27H34O11/c1-32-17-6-4-13(8-19(17)33-2)25-15-11-36-26(16(15)12-35-25)14-5-7-18(20(9-14)34-3)37-27-24(31)23(30)22(29)21(10-28)38-27/h4-9,15-16,21-31H,10-12H2,1-3H3/t15-,16-,21+,22+,23-,24+,25-,26+,27+/m0/s1

1 reference

Phillyrin (English)

8 October 2016

2 references

Phillyrin (English)

8 October 2016

ChEBI release 2020-09-01

2 references

Forsythin (English)

8 October 2016

https://commonchemistry.cas.org/detail?cas_rn=487-41-2

8 April 2021

1 reference

phyllyrin (English)

8 October 2016

2 references

Phillyrin (English)

8 October 2016

ChEBI ID

80888

mapping relation type

2 references

Forsythin (English)

8 October 2016

International Chemical Identifier

InChI

InChI=1S/C27H34O11/c1-32-17-6-4-13(8-19(17)33-2)25-15-11-36-26(16(15)12-35-25)14-5-7-18(20(9-14)34-3)37-27-24(31)23(30)22(29)21(10-28)38-27/h4-9,15-16,21-31H,10-12H2,1-3H3/t15-,16-,21+,22+,23-,24+,25-,26+,27+/m0/s1

SureChEMBL ID

SCHEMBL710957

2 references

based on heuristic

inferred from InChIKey

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

1 reference

2 references

DSSTOX compound identifier

0 references

2 references

Global Substance Registration System

UNII

VE9P4964MG

PHILLYRIN (English)

8 October 2016

0 references

1 reference

Forsythin (English)