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Sigma-Aldrich

Secoisolariciresinol

≥95.0% (HPLC)

Synonym(e):

(2R*,3R*)-2,3-Bis-(4-hydroxy-3-methoxybenzyl)-1,4-butandiol

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About This Item

Empirische Formel (Hill-System):
C20H26O6
Molekulargewicht:
362.42
Beilstein:
6611290
EG-Nummer:
249-599-2
MDL-Nummer:
MFCD01075136
UNSPSC-Code:
41116105
PubChem Substanz-ID:
329758917
NACRES:
NA.21

Assay

≥95.0% (HPLC)

Form

solid

SMILES String

OC[C@@H]([C@H](CO)CC1=CC=C(O)C(OC)=C1)CC2=CC(OC)=C(O)C=C2

InChI

1S/C20H26O6/c1-25-19-9-13(3-5-17(19)23)7-15(11-21)16(12-22)8-14-4-6-18(24)20(10-14)26-2/h3-6,9-10,15-16,21-24H,7-8,11-12H2,1-2H3/t15-,16-/m0/s1

InChIKey

PUETUDUXMCLALY-HOTGVXAUSA-N

Anwendung

Secoisolariciresinol is a metabolite of secoisolariciresinol diglucoside (SDG), an antioxidant present in flaxseed.

Verpackung

Bottomless glass bottle. Contents are inside inserted fused cone.

Physikalische Form

Enantiomerengemisch des (R*,R*)-Diastereoisomeren

Sonstige Hinweise

Component of functional food. Flaxseed lignan with antioxidant activity

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

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Analysenzertifikate (COA)

Lot/Batch Number
BCCH0033
BCCB5794
BCBR1232V
BCBH3105V
BCBL3009V

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Carol J Fabian et al.
Cancer prevention research (Philadelphia, Pa.), 3(10), 1342-1350 (2010-08-21)
Preclinical and correlative studies suggest reduced breast cancer with higher lignan intake or blood levels. We conducted a pilot study of modulation of risk biomarkers for breast cancer in premenopausal women after administration of the plant lignan secoisolariciresinol given as
Shiori Tominaga et al.
Food & function, 3(1), 76-82 (2011-10-28)
Flaxseed lignan, secoisolariciresinol has been reported to possess health benefits. We previously synthesized each stereoisomer of secoisolariciresinol and found that (-)-secoisolariciresinol reduces lipid accumulation and induces adiponectin production in 3T3-L1 adipocytes. Here we show the effects of (-)-secoisolariciresinol on high-fat
Cheng-Zhi Wang et al.
BMC microbiology, 10, 115-115 (2010-04-20)
The effects of enterolignans, e.g., enterodiol (END) and particularly its oxidation product, enterolactone (ENL), on prevention of hormone-dependent diseases, such as osteoporosis, cardiovascular diseases, hyperlipemia, breast cancer, colon cancer, prostate cancer and menopausal syndrome, have attracted much attention. To date
D D Kitts et al.
Molecular and cellular biochemistry, 202(1-2), 91-100 (2000-03-08)
The antioxidant activities of the flaxseed lignan secoisolariciresinol diglycoside (SDG) and its mammalian lignan metabolites, enterodiol (ED) and enterolactone (EL), were evaluated in both lipid and aqueous in vitro model systems. All three lignans significantly (p < or = 0.05)
Hisashi Nishiwaki et al.
Bioscience, biotechnology, and biochemistry, 75(9), 1735-1739 (2011-09-08)
The larvicidal activity against Culex pipiens of all stereoisomers of dihydroguaiaretic acid (DGA) and secoisolariciresinol was measured, and these DGAs were found to be potent. Sixteen (-)-DGA derivatives were then newly synthesized to analyze their structure-activity relationship. Two derivatives monohydroxylated
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