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- 详细信息
- 技术资料
- 保存条件:
4°C, sealed storage, away from moisture and light
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
2603528-97-6
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥3498.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥1520.0 |
| 规格: | 5 mg | 产品价格: | ¥3800.0 |
| 规格: | 10 mg | 产品价格: | ¥5738.0 |
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ART558
CAS No. : 2603528-97-6
MCE 国际站:ART558
产品活性: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。
研究领域:Cell Cycle/DNA Damage
作用靶点:DNA/RNA Synthesis
In Vitro: ART558 (0~10 μM; 7 days; BRCA2wild-type or BRCA2‒/‒ cells) shows synthetic lethality and a combinatorial effect with the PARPi olaparib in previously described isogenic models of BRCA1-deficiency.
ART558 (5μM; 0~72 hours; BRCA2wild-type or BRCA2‒/‒ cells) shows γH2AX accumulation in cells.
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.
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