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NSC-207895 {[allProObj[0].p_purity_real_show]}

货号:A1153021 同义名: XI-006; NSC 179940

NSC-207895是一种DNA损伤剂,具有抗癌活性并能激活p53。

HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
NSC-207895 化学结构 CAS号:58131-57-0
NSC-207895 化学结构
CAS号:58131-57-0
NSC-207895 3D分子结构
CAS号:58131-57-0
NSC-207895 化学结构 CAS号:58131-57-0
NSC-207895 3D分子结构 CAS号:58131-57-0
规格 价格 会员价 库存 数量
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NSC-207895 纯度/质量文件 产品仅供科研

货号:A1153021 标准纯度: {[allProObj[0].p_purity_real_show]}
批次查询: 批次纯度:

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产品名称 p53 其他靶点 纯度
Pifithrin-μ 99%+
Pifithrin-α HBr 98%
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。

NSC-207895 生物活性

描述 NSC-207895 (XI-006), a DNA damaging agent, serves as an anticancer agent and p53 activator[1][2][3].
体外研究

NSC-207895 (0.5 μM, 30 min), an MDM2 inhibitor, enhances p53 protein levels[2].

NSC-207895, an MDMX inhibitor, reduces MDMX expression in AML cells at both mRNA and protein levels[3].

NSC-207895 细胞实验

Cell Line
Concentration Treated Time Description References
HT1080 cells 5 µM 24 h Inhibited MDMX expression Mol Cancer Ther. 2011 Jan;10(1):69-79.
MCF-7 cells 5 µM 16 h Activated p53 and induced pro-apoptotic gene expression Mol Cancer Ther. 2011 Jan;10(1):69-79.
B6-2 7.29 μM 48 h NSC207895 showed significant cytotoxic and antiproliferative effects in B6-2 cells Sci Rep. 2021 Feb 3;11(1):2967.
HepT1 1.47 μM 48 h NSC207895 showed significant cytotoxic and antiproliferative effects in HepT1 cells Sci Rep. 2021 Feb 3;11(1):2967.
Huh-6 3.03 μM 48 h NSC207895 showed significant cytotoxic and antiproliferative effects in Huh-6 cells Sci Rep. 2021 Feb 3;11(1):2967.
HepG2 0.95 μM 48 h NSC207895 showed significant cytotoxic and antiproliferative effects in HepG2 cells Sci Rep. 2021 Feb 3;11(1):2967.
Osteosarcoma cell lines 2.14–5.41 μM 48 h XI-006 induced cell cycle arrest rather than apoptosis in osteosarcoma cell lines. Sci Rep. 2015 Jun 22;5:11465.
Ewing sarcoma cell lines 0.099–1.61 μM 48 h XI-006 induced potent p53-independent apoptosis in Ewing sarcoma cell lines, independent of MDM4 mRNA/protein levels or TP53 status. Sci Rep. 2015 Jun 22;5:11465.
mouse primary chondrocytes 0.5 μM 6 h NSC-207895 activates p53 and reverses the inhibitory effect of miR-325-3p on mechanical overloading-induced chondrocyte senescence. Arthritis Res Ther. 2023 Apr 4;25(1):54.

NSC-207895 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
Mice HepT1 orthotopic xenograft model Intraperitoneal injection 5 mg/kg Every other day for three weeks NSC207895 significantly decreased tumor weight and increased apoptosis in the treatment group Sci Rep. 2021 Feb 3;11(1):2967.

NSC-207895 参考文献

[1]Laura Kapitzky, et al. Cross-species chemogenomic profiling reveals evolutionarily conserved drug mode of action. Mol Syst Biol. 2010 Dec 21;6:451.

[2]Erdenezaya Odkhuu, et al. Lipopolysaccharide downregulates the expression of p53 through activation of MDM2 and enhances activation of nuclear factor-kappa B. Immunobiology. 2015 Jan;220(1):136-41.

[3]Luis A Carvajal, et al. Dual inhibition of MDMX and MDM2 as a therapeutic strategy in leukemia. Sci Transl Med. 2018 Apr 11;10(436):eaao3003.

NSC-207895 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.58mL

0.72mL

0.36mL

17.91mL

3.58mL

1.79mL

35.81mL

7.16mL

3.58mL

NSC-207895 技术信息

CAS号58131-57-0
分子式C11H13N5O4
分子量 279.25
SMILES Code O=[N+](C1=CC=C(N2CCN(C)CC2)C3=[N+]([O-])ON=C31)[O-]
MDL No. MFCD01660065
别名 XI-006; NSC 179940; NSC-207895, NSC207895, NSC 207895, NSC179940, NSC-179940, NSC 179940, XI-006, XI 006, XI006
运输蓝冰
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Sealed in dry, 2-8°C

溶解方案

DMSO: 30 mg/mL(107.43 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

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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