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Merck

SML0295

Sigma-Aldrich

二氢杨梅素

≥98% (HPLC)

别名:

(2R,3R)-3,5,7-三羟基-2-(3,4,5-三羟基苯基)-2,3-二氢色-4-酮, 3,3′,4′,5,5′,7-六羟基黄烷酮, DHM, 蛇葡萄素

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About This Item

经验公式(希尔记法):
C15H12O8
CAS号:
分子量:
320.25
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

方案

≥98% (HPLC)

表单

powder

储存条件

protect from light

颜色

white to beige

溶解性

DMSO: ≥5 mg/mL (warmed)

储存温度

−20°C

SMILES字符串

O=C1C2=C(O)C=C(O)C=C2O[C@H](C3=CC(O)=C(C(O)=C3)O)[C@H]1O

InChI

1S/C15H12O8/c16-6-3-7(17)11-10(4-6)23-15(14(22)13(11)21)5-1-8(18)12(20)9(19)2-5/h1-4,14-20,22H/t14-,15+/m0/s1

InChI key

KJXSIXMJHKAJOD-LSDHHAIUSA-N

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一般描述

二氢杨梅素是显齿蛇葡萄中的主要类黄酮物质。

应用

二氢杨梅素已用于研究其对分化好的3T3-L1前脂肪细胞中的脂肪生成和葡萄糖摄取的影响。它还用于研究其抗肝癌细胞的抗肿瘤活性。

生化/生理作用

二氢杨梅素 (Ampelopsin) 是一种具有抗氧化和抗癌活性的黄烷醇。
二氢杨梅素 (Ampelopsin) 是一种具有抗氧化和抗癌活性的黄烷醇,具有抗酒精中毒作用。 它的抗酒精作用似乎是由于它在苯并二氮杂卓位点作为 GABA-A受体的正调节剂的作用。
二氢杨梅素具有抗炎作用。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Shimei Qi et al.
International immunopharmacology, 12(1), 278-287 (2011-12-24)
Ampelopsin (AMP), a plant flavonoid, has potent anti-inflammatory properties in vitro and in vivo. The molecular mechanisms of ampelopsin on pharmacological and biochemical actions of RAW264.7 macrophages in inflammation have not been clearly elucidated yet. In the present study, non-cytotoxic
Feng Ni et al.
PloS one, 7(6), e38802-e38802 (2012-06-14)
The objective of this study was to evaluate the chemopreventive effect of a novel flavonoid, ampelopsin (AMP) on the growth and metastasis of prostate cancer cells. AMP showed the more potent activity in inhibiting the proliferation of androgen-sensitive LNCaP and
Dihydromyricetin promotes hepatocellular carcinoma regression via a p53 activation-dependent mechanism
Zhang Q, et al.
Scientific Reports, 4, 4628-4628 (2014)
Wei-Ming Zhou et al.
Molecules (Basel, Switzerland), 15(4), 2114-2123 (2010-04-30)
This study reports two novel 5-fluorouracil-substituted ampelopsin derivatives. The structures of two new derivatives were characterized by elemental analysis, 1H-NMR, 13C-NMR, IR and MS. Their anticancer activities in vitro against two cancer cell lines, K562 and K562/ADR, were investigated using
Tiange Cai et al.
Biological & pharmaceutical bulletin, 34(9), 1501-1507 (2011-09-02)
Stilbenes are a class of compounds that has been reported to inhibit a variety of pathological processes during inflammatory reactions. In this study, cis-ampelopsin E, a stilbene isolated from the seeds of Paeonia suffruticosa, was shown to dose-dependently reduce the

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