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Merck
CN

97326

Supelco

异水飞蓟宾A

analytical standard

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别名:
(2R,3R)-3,5,7-三羟基-2-[(2R,3R)-2-(4-羟基-3-甲氧基苯基)-3-(羟甲基)-2,3-二氢苯并[1,4]二恶英-6-基] -4-苯并二氢吡喃酮
经验公式(希尔记法):
C25H22O10
分子量:
482.44
UNSPSC代码:
85151701
NACRES:
NA.24

等级

analytical standard

质量水平

检测方案

≥95.0% (HPLC)

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

杂质

≤10.0% water

应用

food and beverages

格式

neat

SMILES字符串

COc1cc(ccc1O)[C@H]2Oc3ccc(cc3O[C@@H]2CO)[C@H]4Oc5cc(O)cc(O)c5C(=O)[C@@H]4O

InChI

1S/C25H22O10/c1-32-17-6-11(2-4-14(17)28)24-20(10-26)33-18-7-12(3-5-16(18)34-24)25-23(31)22(30)21-15(29)8-13(27)9-19(21)35-25/h2-9,20,23-29,31H,10H2,1H3/t20-,23+,24-,25-/m1/s1

InChI key

FDQAOULAVFHKBX-HKTJVKLFSA-N

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一般描述

异水飞蓟宾 A 是黄酮木质素,是水飞蓟素中的一种生物活性成分,从 水飞蓟中分离得到。通常用于治疗肝硬化、肝炎、防止肝脏受有毒物质影响。

应用

异水飞蓟宾 B 可作为分析参考标准品,通过高效液相色谱法联合光电二极管阵列检测和电喷雾电离质谱法测定 水飞蓟奶蓟 化合物制剂中的分析物。
有关合适仪器技术的更多信息,请参考产品分析证书。如需进一步支持,请联系技术服务。

包装

无底玻璃瓶。内含物在插入的融合锥体内。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


分析证书(COA)

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Aging is an unavoidable process characterized by gradual failure of homeostasis that constitutes a critical risk factor for several age-related disorders. It has been unveiled that manipulation of various key pathways may decelerate the aging progression and the triggering of
Simultaneous determination of abietane-type diterpenes, flavonolignans and phenolic compounds in compound preparations of Silybum marianum and Salvia miltiorrhiza by HPLC-DAD-ESI MS
Zhao Y, et al.
Journal of Pharmaceutical and Biomedical Analysis, 38(3), 564-570 (2005)
Separation and characterization of silybin, isosilybin, silydianin and silychristin in milk thistle extract by liquid chromatography?electrospray tandem mass spectrometry
Lee.IJ, et al.
Journal of Chromatography A, 1116(1-2), 147-152 (2006)
Jiazeng Yang et al.
Metabolic engineering, 59, 44-52 (2020-02-01)
Silymarin extracted from milk thistle seeds, is used for treating hepatic diseases. Silybin and isosilybin are its main components, and synthesized from coupling of taxifolin and coniferyl alcohol. Here, the biosynthetic pathways of taxifolin and coniferyl alcohol were reconstructed in

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