40043
罗汉松脂酚
≥85% (HPLC)
别名:
(αR,βR)-α,β-双(4-羟基-3-甲氧苯基)丁内酯
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关于此项目
经验公式（希尔记法）:
C20H22O6
化学文摘社编号:
分子量:
358.39
UNSPSC Code:
41116105
NACRES:
NA.21
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
7826317
InChI
1S/C20H22O6/c1-24-18-9-12(3-5-16(18)21)7-14-11-26-20(23)15(14)8-13-4-6-17(22)19(10-13)25-2/h3-6,9-10,14-15,21-22H,7-8,11H2,1-2H3/t14-,15+/m0/s1
SMILES string
COc1cc(C[C@H]2COC(=O)[C@@H]2Cc3ccc(O)c(OC)c3)ccc1O
InChI key
MATGKVZWFZHCLI-LSDHHAIUSA-N
assay
≥85% (HPLC)
storage temp.
2-8°C
Quality Level
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Other Notes
罗汉松脂酚是一种植物雌激素，通常作为膳食补充剂，其代谢物具有雌激素的特征；通常采用 HPLC 测定罗汉松脂酚含量
存储类别
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
L.P. Meagher, G.R. Beecher
J. Food Compos. Anal., 13, 935-935 (2000)
Tanja Kraushofer et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 777(1-2), 61-66 (2002-09-25)
A HPLC method coupled with coulometric electrode array detection for the determination of matairesinol in flax seed is described. The defatted sample was spiked with bisphenol A (internal standard), refluxed for 75 min in a mixture of ethanol-bidistilled water-12 M
Boram Lee et al.
Biochemical and biophysical research communications, 421(1), 76-80 (2012-04-10)
Mitochondrial reactive oxygen species (mROS) are involved in cancer initiation and progression and function as signaling molecules in many aspects of hypoxia and growth factor-mediated signaling. Here we report that matairesinol, a natural small molecule identified from the cell-based screening
Saya Kawahara et al.
Bioscience, biotechnology, and biochemistry, 74(9), 1878-1883 (2010-09-14)
The IgE-suppressive activity of (-)-matairesinol is demonstrated, and the structure-activity relationship of (-)-matairesinol clarified. 3',4-Dihydroxy-3,4'-dimethoxylignano-9,9'-lactone showed higher IgE-suppressive activity than (-)-matairesinol without any cytotoxic activity. Some derivatives bearing a longer and more bulky alkoxy group at the 3 or 4
Johanna W Lampe et al.
Journal of AOAC International, 89(4), 1174-1181 (2006-08-19)
Phytoestrogens occur naturally in plants and are structurally similar to mammalian estrogens. The lignans are a class of phytoestrogen and can be metabolized to the biologically active enterolignans, enterodiol, and enterolactone by a consortium of intestinal bacteria. Secoisolariciresinol diglucoside (SDG)
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