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SMB00181

Sigma-Aldrich

Liriodendrin

≥85% (LC/MS-ELSD)

Synonym(s):

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

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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

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Certificates of Analysis (COA)

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

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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
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
Tomoko Sano et al.
Journal of natural medicines, 64(3), 257-265 (2010-03-11)
Boi and its original plant Sinomenium acutum from Japan were compared with Seifuto and its botanical origins from China in terms of their internal transcribed spacer (ITS) sequences and major chemical components. Boi, Seifuto, and their botanical origins overall showed
Yan-ru Deng et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 30(4), 272-274 (2005-02-24)
To study the chemical constituents from Lamium maculatum var. kansuense. The chemical constituents were isolated and repeatedly purified on silica gel column and the structures were elucidated by the NMR spectra and physico-chemical properties. Six compounds were obtained and identified
Chun Feng et al.
Archives of pharmacal research, 33(12), 1927-1932 (2010-12-31)
A new triterpene, 21-O-senecioyl-R(1)-barrigenol (1) and 13 known compounds were isolated from the ethanol extracts of the leaves and bark of Pittosporum brevicalyx (Oliv.) Gagnep. Their structures were elucidated based on spectral data. The antiarrhythmic action of one furofuran lignan
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