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重要文件

92136

Supelco

染料木黄酮

analytical standard

同義詞:

4′,5,7-三羟基异黄酮, 5,7-二羟基-3-(4-羟基苯基)-4H-1-苯并吡喃-4-酮

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About This Item

經驗公式(希爾表示法):
C15H10O5
CAS號碼:
分子量::
270.24
Beilstein:
263823
EC號碼:
MDL號碼:
分類程式碼代碼:
85151701
PubChem物質ID:
NACRES:
NA.24

等級

analytical standard

品質等級

化驗

≥97% (HPLC)

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

應用

food and beverages

形式

neat

儲存溫度

2-8°C

SMILES 字串

Oc1ccc(cc1)C2=COc3cc(O)cc(O)c3C2=O

InChI

1S/C15H10O5/c16-9-3-1-8(2-4-9)11-7-20-13-6-10(17)5-12(18)14(13)15(11)19/h1-7,16-18H

InChI 密鑰

TZBJGXHYKVUXJN-UHFFFAOYSA-N

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一般說明

Genistein是一种天然存在的大豆异黄酮,是一种饮食蛋白酪氨酸激酶(PTK抑制剂。目前发现它具有抗癌特性。

應用

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。

生化/生理作用

酪氨酸蛋白激酶抑制剂; 在其他蛋白激酶反应中,ATP的竞争性抑制剂。 抗血管生成剂,可下调参与控制血管生成的基因的转录。

包裝

无底玻璃瓶。内含物在插入的融合锥体内。

其他說明

This compound is commonly found in plants of the genus: glycyrrhiza

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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分析證明 (COA)

Lot/Batch Number

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存取文件庫

Genistein inhibits renal cancer progression through long non-coding RNA HOTAIR suppression
Imai-Sumida M, et al.
Clinical Cancer Research, 3449-3449 (2017)
Genistein inhibits both estrogen and growth factor-stimulated proliferation of human breast cancer cells
GP and SB
Cell Growth & Differentiation : the Molecular Biology Journal of the American Association For Cancer Research, 7, 1345-1351 (1996)
Alexandra Mamagkaki et al.
PloS one, 16(4), e0250599-e0250599 (2021-04-28)
The objective of this study is to improve and optimize the formulation of Genistein in capsules in order to result in a better pharmacokinetic profile comparing to existing commercial products. In order to do this, five different formulations of Genistein
Sonia de Pascual-Teresa et al.
The Journal of nutritional biochemistry, 17(4), 257-264 (2005-08-20)
If soy isoflavones are to be effective in preventing or treating a range of diseases, they must be bioavailable, and thus understanding factors which may alter their bioavailability needs to be elucidated. However, to date there is little information on
M Uehara et al.
The Journal of steroid biochemistry and molecular biology, 72(5), 273-282 (2000-05-24)
A time-resolved fluoroimmunoassay (TR-FIA), with europium labeled phytoestrogens as tracers, was developed for the quantitative determination of enterolactone, genistein and daidzein in human urine. The aim was to create a method for the screening of large populations in order to

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