跳转至内容
Merck
CN

A281

Sigma-Aldrich

芹菜素

solid

别名:

4 & # 8242;,5,7-三羟基黄酮, 5,7-二羟基-2-(4-羟基苯基)-4-苯并吡喃酮

登录查看公司和协议定价

选择尺寸


关于此项目

经验公式(希尔记法):
C15H10O5
化学文摘社编号:
分子量:
270.24
Beilstein:
262620
EC 号:
MDL编号:
UNSPSC代码:
12171500
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

表单

solid

颜色

yellow to green

mp

>300 °C (lit.)

溶解性

DMSO: 27 mg/mL
H2O: insoluble

SMILES字符串

Oc1ccc(cc1)C2=CC(=O)c3c(O)cc(O)cc3O2

InChI

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

InChI key

KZNIFHPLKGYRTM-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

生化/生理作用

一种植物类黄酮,研究发现它通过在G2/M阶段阻止细胞周期来抑制细胞增殖。通过细胞周期停滞和诱导凋亡来抑制生长似乎与p53的诱导有关。对肿瘤促进的抑制作用也可能是由于激酶活性的抑制以及由此导致的癌基因表达的抑制。研究还报道了抑制拓扑异构酶ⅰ催化的脱氧核糖核酸再附着和增强细胞间缝隙连接通讯。
一种植物类黄酮,研究发现它通过在G2/M阶段阻止细胞周期来抑制细胞增殖。通过细胞周期停滞和诱导凋亡来抑制生长似乎与p53的诱导有关。通过抑制蛋白激酶C和由此导致的癌基因表达抑制来抑制PMA介导的肿瘤促进。研究还报道了抑制拓扑异构酶ⅰ催化的脱氧核糖核酸再连接和增强间隙连接细胞间通讯。

法规信息

新产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our 文件 section.

如需帮助,请联系 客户支持

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Gao-Jun Fan et al.
Bioorganic & medicinal chemistry letters, 17(24), 6720-6722 (2007-10-30)
The bioassay-guided purification of ether extracts of Alpinia officinarum led to the isolation of two new compounds 6-hydroxy-1,7-diphenyl-4-en-3-heptanone (1) and 6-(2-hydroxy-phenyl)-4-methoxy-2-pyrone (4) as well as three known compounds 1,7-diphenyl-4-en-3-heptanone (2), 1,7-diphenyl-5-methoxy-3-heptanone (3), and apigenin (5). Their structures were established on
Iris L K Wong et al.
Antimicrobial agents and chemotherapy, 51(3), 930-940 (2006-12-30)
Drug resistance by overexpression of ATP-binding cassette (ABC) transporters is an impediment in the treatment of leishmaniasis. Flavonoids are known to reverse multidrug resistance (MDR) in Leishmania and mammalian cancers by inhibiting ABC transporters. Here, we found that synthetic flavonoid
Heshu Lu et al.
Journal of medicinal chemistry, 48(3), 737-743 (2005-02-04)
Cyclin-dependent kinases (CDKs) play a central role in cell cycle control, apoptosis, transcription, and neuronal functions. They are important targets for the design of drugs with antimitotic or antineurodegenerative effects. CDK4 and CDK6 form a subfamily among the CDKs in
Kee Dong Yoon et al.
Journal of natural products, 70(12), 2029-2032 (2007-11-13)
Three new flavonoid glycosides ( 1- 3), 11-hydroxyhainanolidol ( 4), and a new dibenzylbutyrolactone lignan glycoside ( 5) were isolated from the aerial parts of Cephalotaxus koreana Nakai, along with 19 known flavonoids. The structures of the new compounds were
Veljko Veljkovic et al.
Bioorganic & medicinal chemistry letters, 17(5), 1226-1232 (2006-12-27)
Flavonoid compounds represent an important natural source of antiretrovirals for AIDS therapy due to their significant anti-HIV-1 activity and low toxicity. Here we propose a simple theoretical criterion to discriminate active from inactive flavonoids that is suitable for rapid in

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持