NSC745885,98.0%

产品编号:Bellancom-119198| CAS NO:4219-52-7| 分子式:C14H6N2O2S| 分子量:266.27

本网站销售的所有产品仅用于工业应用或者科学研究等非医疗目的,不可用于人类或动物的临床诊断或者治疗,非药用,非食用,

货号 包装 价格 库存与货期 购买量 操作
Bellancom-119198
2500.00 杭州 北京(现货)
Bellancom-119198
4500.00 杭州 北京(现货)
Bellancom-119198
13000.00 杭州 北京(现货)
Bellancom-119198
18000.00 杭州 北京(现货)

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NSC745885

产品介绍 NSC745885 是一种有效的抗肿瘤 (anti-tumor) 试剂,对多种癌细胞株有选择性毒性,但对正常细胞没有毒性。NSC745885 是一种有效的 EZH2 的下调因子通过蛋白酶体降解途径。NSC745885 为晚期膀胱癌和口腔鳞癌的研究提供了可能性。
生物活性

NSC745885 an effective anti-tumor agent, shows selective toxicity against multiple cancer cell lines but not normal cells. NSC745885 is an effective down-regulator of EZH2 via proteasome-mediated degradation. NSC745885 provides possibilities for the study of advanced bladder and oral squamous cell carcinoma (OSCC) cancers.

体外研究

NSC745885 (0.5-4 μM; 24, 48 or 72 hours) has a growth inhibitory or death-promoting effect on the SAS cells, it significantly decreases the densities of cultured cells when compared with untreated cells. The IC50 of NSC745885 is 0.85 μM after 72 hours’ treatment.
NSC745885 (0.5-4 μM; 24 hours) increases annexin V positive cells in a dose-dependent manner, and the differences appears as a dose-dependent manner.
NSC745885 (0.5-2 μM; 24 or 48 hours) decreases XIAP protein levels and increases protein levels both as a dose-dependent manner in SAS cells.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay

Cell Line: SAS cells is obtained from a poorly differentiated human squamous cell carcinoma
Concentration: 0.5 μM, 1 μM, 1.5 μM, 2 μM, 4 μM
Incubation Time: 24, 48, or 72 hours
Result: Decreases SAS cells growth as a time and dose-dependent manner.

Apoptosis Analysis

Cell Line: SAS cells is obtained from a poorly differentiated human squamous cell carcinoma
Concentration: 0.5 μM, 1 μM, 1.5 μM, 2 μM, 4 μM
Incubation Time: 24 hours
Result: Decreases SAS cells growth as a time and dose-dependent manner.

Western Blot Analysis

Cell Line: SAS cells is obtained from a poorly differentiated human squamous cell carcinoma
Concentration: 0.5 μM, 1 μM, 1.5 μM, 2 μM
Incubation Time: 24 or 48 hours
Result: Increased cleaved caspase-3 expression and decreased XIAP expression.
体内研究
(In Vivo)

NSC745885 (intraperitoneal injection; 2 mg/kg; once daily; 10 days) treatment significantly reduces tumor size when compared with the vehicle control, and exhibits a higher safety than doxorubicin.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Eight-week-old NOD/SCID (NOD.CB17 Prkdcscid/J) mice
Dosage: 2 mg/kg
Administration: Intraperitoneal injection; 2 mg/kg; once daily; 10 days
Result: Inhibited engrafted tumors growth in vivo.
体内研究

NSC745885 (intraperitoneal injection; 2 mg/kg; once daily; 10 days) treatment significantly reduces tumor size when compared with the vehicle control, and exhibits a higher safety than doxorubicin.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Eight-week-old NOD/SCID (NOD.CB17 Prkdcscid/J) mice
Dosage: 2 mg/kg
Administration: Intraperitoneal injection; 2 mg/kg; once daily; 10 days
Result: Inhibited engrafted tumors growth in vivo.
体内研究

NSC745885 (intraperitoneal injection; 2 mg/kg; once daily; 10 days) treatment significantly reduces tumor size when compared with the vehicle control, and exhibits a higher safety than doxorubicin.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Eight-week-old NOD/SCID (NOD.CB17 Prkdcscid/J) mice
Dosage: 2 mg/kg
Administration: Intraperitoneal injection; 2 mg/kg; once daily; 10 days
Result: Inhibited engrafted tumors growth in vivo.
性状Solid
溶解性数据
In Vitro: 

DMSO : < 1 mg/mL (insoluble or slightly soluble)

*NSC745885 is usually formulated as a suspension.

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
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