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Voreloxin HCl {[allProObj[0].p_purity_real_show]}

货号:A405214 同义名: AG 7352 Hydrochloride;Vosaroxin Hydrochloride

Voreloxin HCl is a naphthyridine analogue with antineoplastic activity and an inhibitor of Topo II.

Voreloxin HCl 化学结构 CAS号:175519-16-1
Voreloxin HCl 化学结构
CAS号:175519-16-1
Voreloxin HCl 3D分子结构
CAS号:175519-16-1
Voreloxin HCl 化学结构 CAS号:175519-16-1
Voreloxin HCl 3D分子结构 CAS号:175519-16-1
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Voreloxin HCl 纯度/质量文件 产品仅供科研

货号:A405214 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 Topo I Topo II Topo IV Topoisomerase 其他靶点 纯度
Ellagic acid 98%
β-Lapachone 99%+
(s)-10-hydroxycamptothecin 98+%
Camptothecin ++

Topo I, IC50: 0.68 μM

98%
Betulinic acid ++

Eukaryotic topoisomerase I, IC50: 5 μM

98%
Topotecan ++++

Topo I (DU-145 Luc cells), IC50: 2 nM

Topo I (MCF-7 Luc cells), IC50: 13 nM

98%
Irinotecan HCl Trihydrate 98%
SN-38 98%
Levofloxacin hydrate 98%
Dexrazoxane 99%+
Ofloxacin 98+%
Enoxacin 99%+
Flumequine +

Topo II, IC50: 15 μM

98%
Levofloxacin 97%
Etoposide 98%
Pefloxacin mesylate dihydrate 99+%
Marbofloxacin 98+%
Voreloxin HCl 98%
Mitoxantrone dihydrochloride PKC 98%
Nalidixic acid 98%
Doxorubicin 98%
Novobiocin sodium 95%
Amonafide 99%+
Pirarubicin 98%+
Idarubicin HCl +++

Topo II (MCF-7 cells), IC50: 3.3 ng/mL

99%+
Genistein EGFR 98%
Teniposide 98%
Moxifloxacin 98%
Ciprofloxacin 98%
Clinafloxacin 97%
Gatifloxacin 98%
Daunorubicin HCl +++

DNA synthesis, Ki: 20 nM

98%
Epirubicin HCl 99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Voreloxin HCl 生物活性

靶点
  • Topo II

描述 Voreloxin hydrochloride is a naphthyridine analogue with antineoplastic activity and an inhibitor of Topo II.

Voreloxin HCl 参考文献

[1]Hoch U, Lynch J, et al. Voreloxin, formerly SNS-595, has potent activity against a broad panel of cancer cell lines and in vivo tumor models. Cancer Chemother Pharmacol. 2009 Jun;64(1):53-65.

[2]Tsuzuki Y, Tomita K, et al. Synthesis and structure-activity relationships of novel 7-substituted 1,4-dihydro-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acids as antitumor agents. Part 2. J Med Chem. 2004 Apr 8;47(8):2097-109.

Voreloxin HCl 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.28mL

0.46mL

0.23mL

11.42mL

2.28mL

1.14mL

22.84mL

4.57mL

2.28mL

Voreloxin HCl 技术信息

CAS号175519-16-1
分子式C18H20ClN5O4S
分子量 437.901
别名 AG 7352 Hydrochloride;Vosaroxin Hydrochloride;Vosaroxin;SNS-595 Hydrochloride;Voreloxin Hydrochloride
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Inert atmosphere,Store in freezer, under -20°C

溶解度

DMSO: 2 mg/mL(4.57 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 2 mg/mL(4.57 mM),配合低频超声,并水浴加热至45℃助溶

动物实验配方
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