PND-1186 hydrochloride (Synonyms: VS-4718 hydrochloride; SR-2516 hydrochloride)
目录号: PL03813 纯度: ≥98%
CAS No. :1356154-94-3
商品编号 规格 价格 会员价 是否有货 数量
PL03813-5mg 5mg ¥1360.00 请登录
PL03813-10mg 10mg ¥1854.55 请登录
PL03813-50mg 50mg ¥5192.73 请登录
PL03813-100mg 100mg ¥9272.73 请登录
PL03813-200mg 200mg 询价 询价
PL03813-500mg 500mg 询价 询价
PL03813-10mM*1mLinDMSO 10mM*1mLinDMSO ¥1609.75 请登录
Medlife所售产品仅用于科学研究(非临床研究),非药品不可食用,不可用于人体或动物的临床诊断和治疗,我们不为个人提供产品及服务。产品COA等资料,可至下方“质量控制”中下载。
中文名称
PND-1186 hydrochloride
英文名称
PND-1186 hydrochloride
英文别名
S803K9N9TL;2-(2-(2-Methoxy-4-morpholinophenylamino)-5-(trifluoromethyl)pyridine-4-ylamino)-N-methylbenzamide hydrochloride;Benzamide, 2-((2-((2-methoxy-4-(4-morpholinyl)phenyl)amino)-5-(trifluoromethyl)-4-pyridinyl)amino)-N-methyl-, hydrochloride (1:1);PND-1186 hydrochloride
Cas No.
1356154-94-3
分子式
C25H27ClF3N5O3
分子量
537.96
包装储存
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
产品详情
PND-1186 hydrochloride (VS-4718 hydrochloride) 是一种有效的,高特异性的,可逆的 FAK 抑制剂,IC50 为 1.5 nM。PND-1186 hydrochloride 选择性促进肿瘤细胞凋亡 (apoptosis)。
生物活性
PND-1186 hydrochloride (VS-4718 hydrochloride) is a potent, highly-specific and reversible inhibitor of FAK with an IC 50 of 1.5 nM. PND-1186 hydrochloride selectively promotes tumor cell apoptosis.
性状
Solid
体外研究(In Vitro)
PND-1186 has an IC50 of ~100 nM in breast carcinoma cells as determined by anti-phospho-specific immunoblotting to FAK Tyr-397.
In murine 4T1 breast carcinoma cells, FAK is important in promoting an invasive and metastatic cell phenotype. Increasing concentrations of PND-1186 (0.1 to 1.0 μM) added to 4T1 cells inhibits FAK Tyr-397 phosphorylation (pY397) and results in elevated levels of total FAK protein within 1 h. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
PND-1186 (30 mg/kg or 100 mg/kg; subcutaneously; injected subcutaneously in the neck region) inhibits 4T1 subcutaneous tumor growth by induction of apoptosis. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
ClinicalTrial
参考文献
[1]. Tanjoni I, et al. PND-1186 FAK inhibitor selectively promotes tumor cell apoptosis in three-dimensional environments. Cancer Biol Ther. 2010 May 15;9(10):764-77.
溶解度数据
In Vitro: DMSO : 200 mg/mL (371.77 mM; Need ultrasonic)H2O : 20 mg/mL (37.18 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2