| CAS NO: | 1198097-97-0 |
| 包装 | 价格(元) |
| 10mM (in 1mL DMSO) | 电议 |
| 10mg | 电议 |
| 50mg | 电议 |
| Physical Appearance | A solid |
| Storage | Store at -20°C |
| M.Wt | 220.25 |
| Cas No. | 1198097-97-0 |
| Formula | C10H8N2O2S |
| Solubility | insoluble in EtOH; insoluble in H2O; ≥9.3 mg/mL in DMSO |
| Chemical Name | (Z)-5-(4-hydroxybenzylidene)-2-imino-2,5-dihydrothiazol-4-ol |
| Canonical SMILES | N=C1N=C(O)/C(S1)=C([H])/C2=CC=C(O)C=C2 |
| 运输条件 | 蓝冰运输或根据您的需求运输。 |
| 一般建议 | 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。不同厂家不同批次产品溶解度各有差异，仅做参考。若实验所需浓度过大至产品溶解极限，请添加助溶剂助溶或自行调整浓度。溶液形式一般不宜长期储存，请尽快用完。 |
Mirin is a potent MRN complex inhibitor. Mirin inhibits Mre11-associated exonuclease activity, rather than alters DNA-binding or MRN complex formation. Moreover, mirin prevents MRN-dependent activation of ATM in response to DNA double-strand breaks, with an IC50 value of 12 μM. The MRN complex acts as a DNA damage sensor, responsible for maintaining genome stability during DNA replication, promoting homology-dependent DNA repair and activating ATM. The MRN-ATM pathway plays an essential role in sensing and signaling from DNA double-strand breaks.
Reference:
1. Dupré A, Boyer-Chatenet L, Sattler RM, et al. A forward chemical genetic screen reveals an inhibitor of the Mre11-Rad50-Nbs1 complex. Nature Chemical Biology, 2008, 4(2): 119-125.
| Cell experiment:[1] | |
Cell lines | Human embryonic kidney (HEK)293 cells and TOSA4 cells |
Reaction Conditions | 10 ~ 100 μM mirin for 24 h incubation |
Applications | In mammalian cells, mirin induced G2 arrest, abolished the radiation-induced G2/M checkpoint, and prevented homology-directed repair of DNA damage. |
Note | The technical data provided above is for reference only. |
References: 1. Dupré A, Boyer-Chatenet L, Sattler RM, et al. A forward chemical genetic screen reveals an inhibitor of the Mre11-Rad50-Nbs1 complex. Nature Chemical Biology, 2008, 4(2): 119-125. | |
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