Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

SMB00181

Sigma-Aldrich

Liriodendrin

≥85% (LC/MS-ELSD)

Synonym(s):

(+)-Syringaresinol di-O-β-glucopyranoside, Acanthoside D

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C34H46O18
CAS Number:
573-44-4
Molecular Weight:
742.72
UNSPSC Code:
12352200
PubChem Substance ID:
329824847
NACRES:
NA.25

Assay

≥85% (LC/MS-ELSD)

form

solid

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−20°C

SMILES string

COc1cc(cc(OC)c1O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]3OCC4C3CO[C@@H]4c5cc(OC)c(OC6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)c(OC)c5

InChI

1S/C34H46O18/c1-43-17-5-13(6-18(44-2)31(17)51-33-27(41)25(39)23(37)21(9-35)49-33)29-15-11-48-30(16(15)12-47-29)14-7-19(45-3)32(20(8-14)46-4)52-34-28(42)26(40)24(38)22(10-36)50-34/h5-8,15-16,21-30,33-42H,9-12H2,1-4H3/t15-,16-,21+,22+,23+,24+,25-,26-,27+,28+,29+,30+,33-,34?/m0/s1

InChI key

FFDULTAFAQRACT-MEAGMGCTSA-N

General description

Natural product derived from plant source.

Biochem/physiol Actions

Liriodendrin has shown anti-inflammatory and antinociceptive properties, the administration of liriodendrin caused a reduction in acute paw edema induced by carrageenan in rats.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
122228321V
122228135V
122228-135V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Jian-fei Chao et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 31(13), 1078-1080 (2006-10-20)
To investigate the chemical constituents from the branch of Broussonetia papyrifera. Column chromatographic methods were used to isolate the chemical constituents. ESI-MS and NMR methods were employed for their structural elucidation. Six compounds were isolated and identified as (2S)-7, 3'-dihydroxy-4'-methoxyflavan
Chu Van Men et al.
Archives of pharmacal research, 34(12), 2065-2071 (2012-01-03)
A quantitative and pattern recognition analyses were conducted for quality evaluation of Kalopanacis Cortex (KC) using HPLC. For quantitative analysis, four bioactive compounds, liriodendrin, pinoresinol O-β-D-glucopyranoside, acanthoside B and kalopanaxin B, were determined. The analysis method was optimized and validated
Hyun-Ju Jung et al.
Planta medica, 69(7), 610-616 (2003-08-05)
In the present study, liriodendrin isolated by activity-guided fractionation from the ethyl acetate (EtOAc) extracts of the stem bark of Acanthopanax senticosus, was evaluated for anti-inflammatory and antinociceptive activities. Liriodendrin (5, 10 mg/kg/day, p. o.) significantly inhibited the increase of
Gang-li Wang et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 27(3), 199-201 (2003-05-31)
To demonstrate the chemical constituents of Alyxia sinensis. The constituents were isolated by column chromatography and identified by advanced physical and spectral analysis. Eight compounds have been isolated and elucidated as bauereny acetate(18), scopletin(19), liriodendrin(20), pinoresinol-di-O-beta-D-glucopyranoside(21), daucosterol(22), flaxetin(23), esculin(24), aseculin(25).
Qiu-ling Fan et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 33(22), 2636-2639 (2009-02-17)
To study the chemical constituents of Eriophyton wallichii. Compounds were separated and purified by column chromatographic methods, and their structures were elucidated by spectroscopic methods. Eight phenylpropanoids were isolated and identified as martynoside (1), leucosceptoside A (2), citrusin B (3)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service