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Merck
CN

440025

Luteolin

≥90% (HPLC), antioxidant flavonoid, solid

别名:

Luteolin, 3ʹ,4ʹ,5,7-Tetrahydroxyflavone

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关于此项目

经验公式(希尔记法):
C15H10O6
化学文摘社编号:
分子量:
286.24
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77
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产品名称

Luteolin, An antioxidant flavonoid and a free radical scavenger.

质量水平

描述

Merck USA index - 14, 5614

方案

≥90% (HPLC)

表单

solid

制造商/商品名称

Calbiochem®

储存条件

OK to freeze
protect from light

颜色

yellow

溶解性

aqueous base: 1.4 mg/mL
DMSO: 7 mg/mL
ethanol: soluble

运输

ambient

储存温度

2-8°C

SMILES字符串

[o]1c2c([c](cc1c3cc(c(cc3)O)O)=O)c(cc(c2)O)O

InChI

1S/C15H10O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-6,16-19H

InChI key

IQPNAANSBPBGFQ-UHFFFAOYSA-N

一般描述

An antioxidant flavonoid and a free radical scavenger. Inhibits rat liver cytosolic glutathione S-transferase activity. Also shows cytotoxic effects on Raji lymphoma cells. Incubation of the non-tumor cell line C3H10T½CL8 with luteolin results in induction of p53 accumulation and apoptosis, with apoptosis occurring at the G2/M phase of the cell cycle. Also shown to inhibit TPL2 kinase.

生化/生理作用

Cell permeable: no
Primary Target
rat liver cytosolic glutathione S-transferase activity
Product does not compete with ATP.
Reversible: no

包装

Packaged under inert gas

制备说明

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 4 weeks at -20°C.

其他说明

Kim, J.E., et al. 2011. J. Pharmacol. Exp. Ther.in press.
Korkina, L.G., and Afanasev, I.B. 1997. Adv. Pharmacol.38, 151.
Plaumann, B., et al. 1996. Oncogene 13, 1605.
Ramanathan, R., et al. 1994. Free Radic. Biol. Med.16, 43.
Shimoi, L., et al. 1994. Carcinogenesis15, 2669.

法律信息

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

免责声明

Toxicity: Standard Handling (A)

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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