| 产品描述： | VE-822 has been used in trials studying the treatment of Ovarian Neoplasms, Ovarian Serous Tumor, Adult Solid Neoplasm, Advanced Solid Tumor, and Advanced Solid Neoplasm, among others. |
| 靶点： |
ATM/ATR |
| 体内研究： |
80 nM VE-822单独使用增加MiaPaCa-2和PSN-1细胞停留在G1期的比率。80 nM VE-822消除MiaPaCa-2和PSN-1细胞中富含XRT的G2/M期部分。VE-822单独作用不大,而80 nM VE-822与XRT和/或gemcitabine联用则增强PSN-1细胞中的早期和晚期细胞凋亡。VE-822增加对与pChk1 Ser345阻断相关的DNA损伤剂的肿瘤应答。VE-822（80 nM）减弱ATR信号传导途径并降低肿瘤细胞对XRT和吉西他滨的应答的存活率。在正常细胞中,80 nM VE-822减弱ATR信号通路强度,但并没有增强辐射和gemcitabine杀伤正常细胞的能力 |
| 细胞实验： |
VE-822 is dissolved in DMSO and stored, and then diluted with appropriate media before use. Gemcitabine (10 nM) is added 24 h pre-XRT and is replaced with fresh medium before addition of VE-822. PSN-1 cells are treated with VE-822 (80 nM) for 1 h before, through to 18 h after, XRT (6 Gy). Apoptosis is analyzed 48 h after XRT by flow cytometry using an Annexin V-FITC kit with Pl |
| 参考文献： |
1.Fokas E, et al. Cancer Treat Rev, 2013, pii: S0305-7372(13)00065-0. 2.Fokas E, et al. Cell Death Dis, 2012, 3, e441. 3.Konstantinopoulos P A , Cheng S C , Hendrickson A E W , et al. Berzosertib plus gemcitabine versus gemcitabine alone in platinum-resistant high-grade serous ovarian cancer: a multicentre, open-label, randomised, phase 2 trial[J]. The Lancet Oncology, 2020, 21(7). |
| 溶解性： |
DMSO:34 mg/mL (73.3 mM) Ethanol:<1 mg/mL |
| 保存条件： |
2-8℃ |
| 配置溶液浓度参考： |
|
1mg |
5mg |
10mg |
| 1 mM |
2.157 ml |
10.786 ml |
21.573 ml |
| 5 mM |
0.431 ml |
2.157 ml |
4.315 ml |
| 10 mM |
0.216 ml |
1.079 ml |
2.157 ml |
| 50 mM |
0.043 ml |
0.216 ml |
0.431 ml |
|
| 注意： |
部分产品我司仅能提供部分信息，我司不保证所提供信息的权威性，仅供客户参考交流研究之用。 |
上海工商
危险品化学品经营许可证（不带存储）
营业执照(三证合一)
北京