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Merck
CN

79851

Sigma-Aldrich

山奈酚3-β-D-吡喃葡萄糖苷

≥97.0% (HPLC)

别名:

3,4′,5,7-四羟基黄酮3-葡萄糖苷, 3-(β-D-吡喃葡糖基)-5,7-二羟基-2-(4-甲氧基苯基)-4H-1-苯并吡喃-4-酮, 3-葡萄糖基山奈酚, 山萘酚3-葡萄糖苷, 紫云英苷

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关于此项目

经验公式(希尔记法):
C21H20O11
CAS Number:
分子量:
448.38
MDL编号:
UNSPSC代码:
12352205
PubChem化学物质编号:
NACRES:
NA.47
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质量水平

方案

≥97.0% (HPLC)

表单

crystals

储存温度

2-8°C

SMILES字符串

OC[C@H]1O[C@@H](OC2=C(Oc3cc(O)cc(O)c3C2=O)c4ccc(O)cc4)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C21H20O11/c22-7-13-15(26)17(28)18(29)21(31-13)32-20-16(27)14-11(25)5-10(24)6-12(14)30-19(20)8-1-3-9(23)4-2-8/h1-6,13,15,17-18,21-26,28-29H,7H2/t13-,15-,17+,18-,21+/m1/s1

InChI key

JPUKWEQWGBDDQB-QSOFNFLRSA-N

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应用


  • 在泛醌生物合成中的作用:该化合物有助于植物生物化学中关键成分泛醌的苯环结构的生物合成,突出了其在细胞能量生产和植物健康中的重要作用(Soubeyrand et al., 2018)。

生化/生理作用

类似的山奈酚甙降低了Wistar大鼠的食物摄入量和相应的体重增加。未测试葡萄糖苷。

包装

无底玻璃瓶。内含物装在插入的融合锥内。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

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Lot/Batch Number

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Mingsheng Peng et al.
Journal of experimental botany, 59(11), 2933-2944 (2008-06-17)
Plants can survive a limiting nitrogen (N) supply by developing a set of N limitation adaptive responses. However, the Arabidopsis nla (nitrogen limitation adaptation) mutant fails to produce such responses, and cannot adapt to N limitation. In this study, the
Monika A Olszewska et al.
Natural product research, 25(12), 1115-1131 (2011-02-25)
Six phenolics were obtained from the leaves of Prunus padus by activity-guided isolation: isorhamnetin 3-O-β-xylopyranosyl-(1 → 2)-β-galactopyranoside (1), astragalin (2), hyperoside (3), quercetin 3-O-β-xylopyranosyl-(1 → 2)-β-galactopyranoside (4), quercetin 3-O-β-xylopyranosyl-(1 → 2)-β-glucopyranoside (5) and chlorogenic acid (6). The antioxidant potential of 70% methanolic extracts from the flowers
Sailesh Malla et al.
Biotechnology and bioengineering, 110(9), 2525-2535 (2013-04-10)
We report the production of astragalin (AST) from regiospecific modifications of naringenin (NRN) in Escherichia coli BL21(DE3). The exogenously supplied NRN was converted into dihydrokaempferol (DHK) and then kaempferol (KMF) in the presence of flavanone-3-hydroxylase (f3h) and flavonone synthase (fls1)
Dae-won Chung et al.
Journal of the science of food and agriculture, 93(2), 362-367 (2012-07-11)
The application of tea seed extract (TSE) has been widely investigated owing to its biological activities. In this paper, two flavonol triglycosides found in TSE, camelliaside A (CamA) and camelliaside B (CamB), were subjected to hydrolysis in the presence of
Choong Je Ma et al.
Journal of enzyme inhibition and medicinal chemistry, 24(3), 676-679 (2008-10-01)
The n-butanol (n-BuOH) fraction of Orostachys japonicus A. Berger (Crassulaceae) significantly inhibited calpain activity. Through the activity-guided isolation from the n-BuOH fraction, herbacetin 8-O-alpha-D-ribopyranoside (1), kaempferol (2), quercetin (3), afzelin (4), astragalin (5), isoquercetin (6) and quercitrin (7) were obtained.

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