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ART558
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
ART558图片
CAS NO:2603528-97-6
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
200mg电议
500mg电议

产品介绍
ART558 是一种纳摩尔、高效、有选择性、低分子量、变构 DNA 聚合酶活性的Polθ抑制剂(IC50=7.9 nM)。ART558 可用于癌症研究。
生物活性

ART558 is a nanomolar potent, selective, low molecular weight, allosteric DNA polymerase activity ofPolθinhibitor (IC50=7.9 nM). ART558 can be used for the research ofcancer[1].

IC50& Target

IC50: 7.9 nM (Polθ)[1]

体外研究
(In Vitro)

ART558 (0~10 μM; 7 days; BRCA2wild-typeor BRCA2-/-cells) shows synthetic lethality and a combinatorial effect with the PARPi olaparib in previously described isogenic models of BRCA1-deficiency[1].
ART558 (5μM; 0~72 hours; BRCA2wild-typeor BRCA2-/-cells) shows γH2AX accumulation in cells[1].
ART558 inhibits the major Polθ mediated DNA repair process, Theta-Mediated End Joining, without targeting NonHomologous End Joining. ART558 elicits DNA damage and synthetic lethality in BRCA1- or BRCA2-mutant tumour cells and enhances the effects of a PARP inhibitor. ART558 increases biomarkers of single-stranded DNA and synthetic lethality in 53BP1-defective cells whilst the inhibition of DNA nucleases that promote end-resection reversed these effects, implicating these in the synthetic lethal mechanism-of-action. ART558 increases the residence time of YFP-tagged full-length Polθ at sites of laserinduced DNA damage[1].

Cell Viability Assay[1]

Cell Line:BRCA2wild-typeor BRCA2-/-cells
Concentration:0~10 μM
Incubation Time:7 days
Result:Showed synthetic lethality and a combinatorial effect with the PARPi olaparib in previously described isogenic models of BRCA1-deficiency.

Western Blot Analysis[1]

Cell Line:BRCA2wild-typeor BRCA2-/-cells
Concentration:5μM
Incubation Time:0~72 hours
Result:Showed γH2AX accumulation in cells.
分子量

418.41

性状

Solid

Formula

C21H21F3N4O2

CAS 号

2603528-97-6

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture and light

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

溶解性数据
In Vitro: 

DMSO : 170 mg/mL(406.30 mM;Need ultrasonic)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM2.3900 mL11.9500 mL23.9000 mL
5 mM0.4780 mL2.3900 mL4.7800 mL
10 mM0.2390 mL1.1950 mL2.3900 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month (sealed storage, away from moisture and light)。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro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,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制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

  • 1.

    请依序添加每种溶剂: 10% DMSO    90%corn oil

    Solubility: ≥ 5 mg/mL (11.95 mM); Clear solution

    此方案可获得 ≥ 5 mg/mL (11.95 mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 50.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

  • 2.

    请依序添加每种溶剂: 10% DMSO    40%PEG300   5%Tween-80   45% saline

    Solubility: 4.25 mg/mL (10.16 mM); Suspended solution; Need ultrasonic

    此方案可获得 4.25 mg/mL (10.16 mM) 的均匀悬浊液,悬浊液可用于口服和腹腔注射。

    以 1 mL 工作液为例,取 100 μL 42.5 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH2O 中,得到澄清透明的生理盐水溶液
*以上所有助溶剂都可在本网站选购。